Relevant bibliographies by topics / H-111

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Academic literature on the topic 'H-111'

Author: Grafiati
Published: 26 July 2024
Last updated: 28 July 2024

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Journal articles on the topic "H-111"

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ALIPOOR, ZAHRA, ZOHREH GHOLAMZADEH, MAHDI SADEGHI, SOLALEH SEYYEDI, and MORTEZA AREF. "DATA EVALUATION ACQUIRED TALYS 1.0 CODE TO PRODUCE 111In FROM VARIOUS ACCELERATOR-BASED REACTIONS." International Journal of Modern Physics E 20, no. 05 (May 2011): 1307–24. http://dx.doi.org/10.1142/s0218301311018332.

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The Indium-111 physical-decay parameters as a β-emitter radionuclide show some potential for radiodiagnostic and radiotherapeutic purposes. Medical investigators have shown that 111 In is an important radionuclide for locating and imaging certain tumors, visualization of the lymphatic system and thousands of labeling reactions have been suggested. The TALYS 1.0 code was used here to calculate excitation functions of 112/114–118 Sn+p , 110 Cd +3 He , 109 Ag +3 He , 111–114 Cd+p , 110/111 Cd+d , 109 Ag +α to produce 111 In using low and medium energy accelerators. Calculations were performed up to 200 MeV. Appropriate target thicknesses have been assumed based on energy loss calculations with the SRIM code. Theoretical integral yields for all the latter reactions were calculated. The TALYS 1.0 code predicts that the production of a few curies of 111 In is feasible using a target of isotopically highly enriched 112 Cd and a proton energy between 12 and 25 MeV with a production rate as 248.97 MBq·μA-1 · h-1. Minimum impurities shall be produced during the proton irradiation of an enriched 111 Cd target yielding a production rate for 111 In of 67.52 MBq· μA-1 · h-1.
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LU, HUNG-CHIEH, and LOU-SING KAN. "CADMIUM AND PROTON NMR STUDY ON [Cd2(BIS(2-PYRIDYL)FORMAMINE)3]." Biophysical Reviews and Letters 03, no. 04 (October 2008): 491–500. http://dx.doi.org/10.1142/s1793048008000861.

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The structure of a bi - Cd organic complex [ Cd 2(bis(2-pyridyl)formamine)3 or 1], is analyzed thoroughly by 1 H and 113/111 Cd NMR in solution. Only one representative set of pyridyl proton resonance of a total of six pyridines in 1 was observed. The resonance of protons in pyridine ring can be assigned by both 2D COSY and 2D NOESY. Similarly, only one Cd (either 113 Cd or 111 Cd NMR signal was observed too. This indicates that the two Cd atoms in 1 are chemically equivalent. The Cd signal is split by its three neighboring equivalent protons on the bridged carbon atoms ( C a H )3, resulting in a quartet. The 3 J 113 Cd –1 H and 3 J 111 Cd –1 H are 44 and 42 Hz, respectively, measured directly from the spectral pattern. The proton NMR signals of C a H composed from three sources: (1) superimposed doublets arising from Cd – H –113 Cd and Cd – H –111 Cd ; (2) a pseudo triplet from 113 Cd – H –113 Cd , 111 Cd – H –111 Cd and 113 Cd – H –111 Cd and (3) a singlet from those H's surrounded by all non-magnetic Cd atoms. They superimpose and appear as a quintet with intensity ratio of 1:12:38:12:1, explainable by the above constituents and their associated Cd – H splitting analyses. We deduced that the three bis(2-pyridyl)formamidine groups have a three-fold symmetry with respect to the Cd – Cd axis, i.e., the three bis(2-pyridyl)formamidine units are co-planar and spaced 120 degrees from each other based on above observations. This implies the key C a atom exists as a hybrid of two canonical forms (– N = C a H – N – ↔ – N – C a H = N –). As a consequence, 1 does not exhibit chirality. We exemplified that Cd NMR study is well suited for investigating those metalloproteins if the calcium and/or zinc ions contained can be replaced by 113 Cd /111 Cd ions of similar size.
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Pan, Guyue, Yongsheng Zhang, Yonggang Li, Chuanguo Zhang, Zhe Zhao, and Zhi Zeng. "Orientation-dependent behaviors of H dissolution and diffusion near W surfaces: A first-principles study." International Journal of Modern Physics C 28, no. 07 (July 2017): 1750090. http://dx.doi.org/10.1142/s0129183117500905.

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The dissolution and diffusion behaviors of H in the four low-Miller-index W surfaces ((110), (112), (100) and (111)) are systematically studied by the density functional theory approach to understand the orientation dependence of the H bubble distribution on surface. The results show that H accumulation on surface is influenced by H diffusion barrier as well as vacancy and H formation. The barriers of diffusion towards surfaces are larger than that in bulk. It indicates that H is prone to diffuse into the deep in bulk once H dissolves in surface. H is preferred to accumulate on the W(111) surface due to the lower formation energies of vacancy and H comparing to that in bulk. However, W(110) is the resistant surface for forming H bubble due to the higher formation energies of vacancy and H. The results are helpful for understanding the orientation dependence of surface damages on W surface and designing new plasma-facing materials.
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Chorniy, R. "Guilt in compositions of crimes against bases of national safety of Ukraine: problem questions of theory and fixing in a law on criminal responsibility." Herald of criminal justice, no. 3 (2019): 136–50. http://dx.doi.org/10.17721/2413-5372.2019.3/136-150.

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The article is devoted to the investigation of forms and types of guilt in the composition of crimes against the basics of national security of Ukraine. The presence of a number of unresolved issues at the theoretical and legal level on this issue actualizes the need for its scientific elaboration and formulation of proposals to improve the provisions of the law on criminal liability. The purpose of the article is to investigate the problematic issues of forms and types of guilt in crimes against the bases of national security of Ukraine, ways of fixing them in the articles of Section I of the Special part of the Criminal Code of Ukraine and to develop sound proposals for their solution based on the provisions of the doctrine of criminal law. The article presents the existing approaches of doctrinal interpretation by scientists of the provisions on wine, its forms and types, through which the research of this feature in the crimes under Art. Art. 109 - 114-1 of the Criminal Code of Ukraine. It is proved that the most reasonable is the psychological concept of guilt, which promotes the insertion of forms and types of guilt in crimes against the basics of national security with a formal composition, the elucidation of forms of guilt in the warehouses of crimes provided by articles of section I of the Special part of the Criminal Code of Ukraine, in which the legislator directly does not say that it is one of the preconditions for the proper qualification of the act committed by the person. It is proved that the basis for the conclusion about the intentional form of guilt is based on: 1) a direct indication of it in the norm of the law (Part 1 of Article 110 and Part 1 of Article 111 of the Criminal Code of Ukraine); 2) indication of the specific purpose or motives of the criminal behavior (Part 1 of Article 109, Note 1, Part 1 and Part 2 of Article 110-2, Article 113, Part 1 of Article 114 and Article 112 of the Criminal Code of Ukraine) ; 3) combination of the above mentioned features in one norm (Part 1 of Article 110 of the Criminal Code of Ukraine); 4) interpretation of terms used in the dispositions of certain articles and / or through the description in the law of the features of the crime (Part 1 of Article 110, Part 2 of Article 109, Part 1 of Article 110, Part 1 of Article 111, Article 112, Article 113, Part 1 of Article 114 and Part 1 of Article 114-1 of the Criminal Code of Ukraine); 5) interpretation of terms used in other articles of the Special (espionage as a part of state treason) or articles of the General part of the Criminal Code of Ukraine (conspiracy to commit the actions provided for in part 1 of Article 109 of the Criminal Code of Ukraine (Article 26 of the Criminal Code of Ukraine), attempted murder state or public figure (Article 112 of the Criminal Code of Ukraine) (part 1 of Article 15 of the Criminal Code of Ukraine); 6) the orientation of socially dangerous acts. The specifics of constructing all these norms testify to the direct intent of the person who committed the respective crime. On this basis it is substantiated that the lack of specification of intent in part 1 of Art. 111 and Part 1 of Art. 110 of the Criminal Code of Ukraine does not contribute to the clarity of the provisions of the Criminal Code in the specified part, and the direct intent in the composition of these crimes is evidenced by: 1) special purpose (Part 1 of Article 110 of the Criminal Code); 2) the terms used in the dispositions of the said articles (“violation of the order… established by the Constitution of Ukraine” (part 1 of Article 110), “transfer of information…, transition to the enemy's side, rendering… assistance in carrying out subversive activities against Ukraine”) ( Part 1 of Article 111); 3) the focus of socially dangerous action. In order to eliminate the ambiguous interpretation of the provisions of Part 1 of Art. 110 and Part 1 of Art. 111 of the Criminal Code it is proposed to amend them accordingly. The forms and type of guilt in the warehouses of crimes with material composition (Part 3 of Article 110, Part 3 and 4 of Article 110-2, Part 2 of Article 114-1 of the Criminal Code of Ukraine) were not clearly reflected in the relevant rules of the law. It is substantiated that the subject's attitude to socially dangerous consequences (deaths of people (h. 3 Art. 110, h. 2 Art. 114-1), other grave consequences (h. 3 Art. 110, h. 4 Art. 110- 2, Part 2 of Article 114-1) Causing considerable property damage (Part 3 of Article 110-2) can be intentional or negligent.
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Svensson, Ann-Marie, Marko Modiano, Angela Karstadt, Mats Mobärg, Åke Persson, Monica Armini, Peter Boxall, et al. "Reviews and notices." Moderna Språk 94, no. 1 (June 1, 2000): 101–19. http://dx.doi.org/10.58221/mosp.v94i1.9661.

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Includes the following reviews: p. 101. Ann-Marie Svensson. Lightfoot, D., The Development of Language, Acquisition, Change, and Evolution. p. 101-103. Marko Modiano. Ronowicz, E. & Yallop, C. (eds), English: One Language, Different Cultures. p. 103-105. Angela Karstadt. Klintborg, S., The Transience of American English. p. 105-106. Mats Mobärg. Pinker, S., Words and Rules. The Ingredients of Language. p. 106-107. Åke Persson. Cartmell, D. & Whelehan, I. (eds), Adaptations: From Text to Screen, Screen to Text. p. 108. Monica Armini. Rivkin, J. & Ryan, M. (eds), Literary Theory: An Anthology. p. 108-109. Peter Boxall. Paul, R., Dissonant Voices: Literature and Society in Britain from Chaucer to the Present Day. p. 109-110. Maria Proitsaki. Dove, R., On the Bus with Rosa Parks. p. 110-111. Ronald Paul. Arundhati, R., The Cost of Living. p. 111. Sabina Kielow. Chouliaraki, L. & Fairclough, N., Discourse in late Modernity: Rethinking Critical Discourse Analysis. + Mills, S., Discourse. The New Critical Idiom. p. 112-114. Lars-Olof Nyhlén. Ammon, U. Ist deutsch noch internationale Wissenschaftssprache? p. 114-115. Sigurd Rothstein. Treichel, H. -U., Der Verlone. p. 116-117. M. Martin Guiney. Horlitz, M. Germanistische Schlaglichter. p. 118-119. M. Martin Guiney. Conner, T., Chateaubriand's Mémoires d'outre-tombe. A portrait of the Artist as Exile.
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Melkozerova, J. A., and I. K. Gainullin. "Theoretical study of resonant charge exchange between H−ion and adsorbate-covered metal surface Cu(111)/Cu(110) with adsorbates Li+/Na+." Seriya 3: Fizika, Astronomiya, no. 4_2023 (September 20, 2023): 2340504–1. http://dx.doi.org/10.55959/msu0579-9392.78.2340504.

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The influence of the surface type on resonant charge exchange between H−ion with a metal surfaces Cu(111) and Cu(110) covered by adsorbate Li+/Na+has been studied. A model static problem was considered. For modeling, athree-dimensional realization of the wave-packet propagation method was used. The Cu(110) andCu(111) surfaces were described by a pseudopotential, derived from a density functional theory (DFT).An occupation of H− ion, an electron density dynamics and an ion level width were analyzed. As aresult, we obtained that an electron oscillates more in case of the surface Cu(111). Furthermore, the resonant charge exchange is more efficient for Cu(111) surface.
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Wang, Runnan, Qingyan Xu, Xiufang Gong, Xianglin Su, and Baicheng Liu. "Experimental and Numerical Studies on Recrystallization Behavior of Single-Crystal Ni-Base Superalloy." Materials 11, no. 7 (July 19, 2018): 1242. http://dx.doi.org/10.3390/ma11071242.

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The recrystallization (RX) behavior of superalloy during standard solution heat treatment (SSHT) varies significantly with deformation temperature. Single-crystal (SX) samples of Ni-base superalloy were compressed to 5% plastic deformation at room temperature (RT) and 980 °C, and the deformed samples were then subjected to SSHT process which consists of 1290 °C/1 h, 1300 °C/2 h, and 1315 °C/4 h, air cooling. RT-deformed samples showed almost no RX grains until the annealing temperature was elevated to 1315 °C, while 980 °C-deformed samples showed a large number of RX grains in the initial stage of SSHT. It is inferred that the strengthening effect of γ’ phases and the stacking faults in them increase the driving force of RX for 980 °C-deformed samples. The RX grains nucleate and grow in dendritic arms preferentially when the microstructural inhomogeneity is not completely eliminated by SSHT. A model coupling crystal plasticity finite element method (CPFEM) and cellular automaton (CA) method was proposed to simulate the RX evolution during SSHT. One ({111} <110>) and three ({111} <110>, {100} <110>, {111} <112>) slip modes were assumed to be activated at RT and 980 °C in CPFEM calculations, respectively. The simulation takes the inhomogeneous as-cast dendritic microstructure into consideration. The simulated RX morphology and density conform well to experimental results.
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Kjellmer, Göran, Ann-Marie Svensson, Monica Malm, Paul Goulding, Ronald Paul, Nathaniel Chase, Alan McGee, et al. "Reviews and notices." Moderna Språk 92, no. 1 (June 1, 1998): 100–120. http://dx.doi.org/10.58221/mosp.v92i1.9847.

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Includes the following reviews:pp. 100-102. Göran Kjellmer. Hill, J. & Lewis, M. (eds), Dictionary of Selected Collocations. pp. 102-103. Ann-Marie Svensson. Lass, R., Historical linguistics and language change. p. 103. Monica Malm. Cixous, H. & Calle-Gruber, M., Rootprints: Memory and Life Writing. p. 104. Paul Goulding. Storry, M. & Childs, P. (ed.), British Cultural Identities. p. 105. Ronald Paul. Young, G., From Sea to Shining Sea: a present-day journey into America's past. pp. 105-106. Monica Malm. Coupe, L., Myth. pp. 106-107. Nathaniel Chase. Modiano, M., A Mid-Atlantic Handbook. American and British English. p. 107. Alan McGee. Bowen, T., Build Your Business Grammar. pp. 107-108. Alan McGee. Comfort, J., Effective Socializing. pp. 108. Alan McGee. Mackenzie, I., Management and Marketing. pp. 109-110. Edelgard Biedermann. Besch, W., Duzen, Siezen, Titulieren: Zur Anrede im Deutschen heute und gestern. pp. 110-111. Stefan Neuhaus. Cumart, N., Zwei Welten. Gedichte. pp. 112-113. Stefan Neuhaus. Fontane, T., Englischer Sommer. pp. 113-115. Hans-Roland Johnsson. Brown, F., Zola, A Life. pp. 115-118. Karl-Anders Arvidsson. Le Nouveau Petit Robert électronique. pp. 118-120. Gabriella Villagrán Backman. Foster, D.W., Mexican Literature: A History.
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Myerscough, Megan, Wes Chapple, William T. Meteer, and Daniel W. Shike. "22 Effects of Housing Cow-calf Pairs on Drylots vs Pasture on Calf Performance and Behavior Through Weaning." Journal of Animal Science 99, Supplement_1 (May 1, 2021): 24. http://dx.doi.org/10.1093/jas/skab054.042.

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Abstract The objectives were to analyze the effects of housing cow-calf pairs in drylots or pasture on calf performance and behavior through weaning. Simmental × Angus (2 yr; 108/yr; 81 ± 15.3 d postpartum) spring-calving cows were stratified by age, BW, BCS, and calf sex and allotted to six groups/yr. Groups were randomly allotted to 1 of 2 treatments: drylot (DL) or pasture (PAST). Calves in the drylot had ad libitum access to a diet consisting of corn silage, dried distillers grain, corn stalks, dry rolled corn, and soybean hulls. Calves on PAST received creep feed three weeks prior to weaning. Calf BW was measured on d 0, 55, and 110. Calves were fence-line weaned on d 110. Behavior was observed for two days after weaning. Data were analyzed using the MIXED procedure of SAS. Drylot calves had greater (P &lt; 0.01) BW at d 55 and 110. There was treatment by time interactions (P &lt; 0.01) for lying and eating on d 111. More PAST calves were lying at h 2 and 3 and eating at h 11 and 12. More DL calves were lying at h 9, 10, 11, and 12. More DL calves were eating at h 2 and tended to at h 3. There was also a treatment by time interaction (P &lt; 0.01) for vocalizations on d 111. More PAST calves vocalized at h 1, however, DL calves vocalized more at h 4 and tended to at h 5. There was treatment by time interactions (P &lt; 0.01) for eating and walking on d 112. More DL calves were eating at h 2, 3, 4, 7, and 9. More PAST calves were walking at h 1 and 2. There was also a treatment by time interaction (P &lt; 0.01) for vocalizations on d 112. More PAST calves vocalized at h 1 and 10. In conclusion, housing cow-calf pairs in drylots improved preweaning performance and altered postweaning behavior.
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Bauschlicher, Charles W., and Marzio Rosi. "Differentiating between H and F or H and CN on C(111) or Si(111) Surfaces." Journal of Physical Chemistry B 102, no. 13 (March 1998): 2403–5. http://dx.doi.org/10.1021/jp9734742.

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Dissertations / Theses on the topic "H-111"

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Yanagita, Hiroshi. "Adsorbed states of H on Ni(111) and Rh(111) surfaces." 京都大学 (Kyoto University), 2000. http://hdl.handle.net/2433/181137.

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Gorgoi, Mihaela. "Electronic Properties of Phthalocyanines Deposited on H-Si(111)." Doctoral thesis, Universitätsbibliothek Chemnitz, 2007. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200700213.

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Im Rahmen dieser Arbeit wurden vier Phthalocyanine untersucht: Metallfreies-Phthalocyanin (H2Pc), Kupferphthalocyanin (CuPc) und Fluor-substituiertes Phthalocyanin (F4CuPc und F16CuPc). Das Ziel dieser Arbeit ist die Charakterisierung der elektronischen und chemischen Eigenschaften der Grenzflächen zwischen diesen Molekülen und Silizium. Die Moleküle wurden durch organische Molekularstrahldeposition (OMBD) im Ultrahochvakuum auf wasserstoffpassivierte Si(111)-Substrate aufgedampft. Oberflächensensitive Messmethoden wie Photoemissionsspektroskopie (PES), Bremsstrahlung Isochromaten Spektroskopie (BIS oder IPES - Inverse Photoemissionsspektroskopie) und Spektroskopie der Röntgen-Absorptions-Feinstruktur (NEXAFS – Near Edge X-Ray Absorption Fine Structure) wurden zur Charakterisierung eingesetzt. Um eine Zuordnung der verschiedenen Komponenten in PES und IPES zu ermöglichen, wurden Methoden der Dichtefunktionaltheorie zur theoretischen Berechnung eingesetzt. Die Energieniveauanpassung an der Grenzfläche zwischen der organischen Schicht und der H-Si-Grenzfläche, sowie die Transportbandlücke von H2Pc, CuPc, F4CuPc und F16CuPc wurden mit Hilfe von PES und IPES bestimmt. Die NEXAFS-Messungen ermöglichten eine genaue Bestimmung der Molekülorientierung relativ zum Substrat. Die Auswertung der Daten zeigte unterschiedliche Molekülorientierungen in dünnen und dicken Filmen. Diese Änderungen wurden mit dem bandverbiegungsähnlichen Verlauf der HOMO-und LUMO-Positionen in Verbindung gebracht. Zusätzlich zu diesem Verhalten wiesen die Grenzflächen auch einen Grenzflächendipol auf, welcher durch die unterschiedlichen Austrittsarbeiten der Kontaktmaterialien hervorgerufen wird. Der Einfluss des Grads der Flouridierung wird durch eine ähnlichen Zunahme der Elektronenaffinität (EA), der Austrittsarbeit (WF) und der Ionisierungsenergie (IE) bestätigt. Die elektronischen Eigenschaften von Metall/organische-Schicht-Grenzflächen und von organischen Schichten unter Sauerstoffeinfluss wurden mit Hilfe von PES und IPES untersucht. Die Ag/Pc Grenzflächen zeigten eine Mischung aus HOMO-LUMO-Verschiebungen und Grenzflächendipolbildung. An den Ag/H2Pc- und Ag/F16CuPc- Grenzflächen wurde ein Ladungstransferkomplex gebildet. Auf der CuPc-Schicht physisorbiert das Ag lediglich und im Fall von F4CuPc wird Ladung zu Ag transferiert, wobei eine andauernde n-Typ-Dotierung an der Grenzfläche erzeugt wird. In Analogie zum Fall der Pc/H-Si Grenzfläche wiesen die Dipole, die hier gefunden wurden, eine lineare Abhängigkeit von EA, WF und IE auf und können durch die Differenz zwischen den Austrittsarbeiten vorausgesagt werden. Das Verhalten der dicken organischen Schichten unter Sauerstoffeinfluss kann in zwei Gruppen eingeteilt werden. Eine Gruppe, bestehend aus H2Pc und F4CuPc, wies nur schwache Wechselwirkung auf und der Sauerstoff physisorbiert auf der Pc-Schicht. Die beiden anderen Moleküle, CuPc und F16CuPc konnten einer Gruppe starker Wechselwirkung zugeordnet werden. CuPc bildet einen Ladungstransferkomplex mit Sauerstoff und auf F16CuPc wird eine polarisierte Schicht gebildet
In the context of this work four Phthalocyanine were studied: Metal-free Phthalocyanine (H2Pc), Copper Phthalocyanine (CuPc) and fluorine-substituted Phthalocyanine (F4CuPc and F16CuPc). The goal of this work is the electronic and chemical characteristics of the interfaces. The molecules were deposited by organic molecular beam deposition (OMBD) in the ultra high vacuum on hydrogen-passivated Si(111)-Substrate. Surface sensitive techniques such as photoemission spectroscopy (PES), bremsstrahlung isochromate spectroscopy (BIS or IPES - inverse photoemission spectroscopy) and near edge X-ray absorption fine structure spectroscopy (NEXAFS) were used for characterisation. Theoretical computations by density functional theory methods were employed, in order to assign different components in PES and IPES. The energy level alignment at the organic/H-Si interface, as well as the transport gap of H2Pc, CuPc, F4CuPc and F16CuPc were determined by PES and IPES. The NEXAFS measurements determine the exact molecular orientation with respect to the substrate. The evaluation of the data showed different molecular orientation in the thin and thick films. This change was correlated with the band bending like behaviours that emerged at these interfaces. In addition to the band bending like behaviour, the interfaces show also an interface dipole which is driven by the work function difference between the contact materials. The influence of the degree of fluorination is confirmed in the similar increase of the EA, WF and IE. The electronic properties of metal/organic layer interfaces and of organic layer under oxygen influence were examined by PES and IPES. The Ag/Pc interfaces show a mixture of HOMO-LUMO shifts and interface dipole formation. A charge transfer complex is formed in the case of Ag/H2Pc and Ag/F16CuPc interfaces. Ag is physisorbed atop the CuPc. Charge transfers from F4CuPc to Ag creating a continuous n-type doping at the interface. Similar to the Pc/H-Si interfaces the interface dipoles found here show a linear dependence on the EA, WF and IE and can be predicted by the difference in the work functions. The data evaluation of oxygen exposed thick films determined two groups of behaviours. The weak interaction group is represented by H2Pc and F4CuPc, Pcs on which oxygen is physisorbed. The strong interaction group contains the other two molecules CuPc and F16CuPc. CuPc forms a charge transfer complex with oxygen and on top of F16CuPc a polarized layer is formed
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Hugelmann, Martin. "Erzeugung und Charakterisierung metallischer Nanostrukturen auf n-Si(111):H-Einkristalloberflächen." Karlsruhe : Univ.-Verl, 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973495839.

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GUNTHER, ROLF. "Etudes des structures electroniques du si(111)-h(1x1) par photoemission angulaire." Paris 11, 1997. http://www.theses.fr/1997PA112443.

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Les etudes de photoemission fourni les resultats suivants : _ la surface si(111)-h(1x1) obtenue par voie chimique est effectivement d'une qualite esceptionelle. _ la preparation de la surface par voie chimique n'est pas completement maitrisee. Nous avons travaille sur une quarantaine d'echantillons : deux ou trois ont presente des spectres nettement superieurs aux autres. L'origine de cette difference n'est pas evidente. _ la finesse des raies a permis d'obtenir la position des etats de surfaces dans la bande de valanece ainsi que leur dispersion avec une grande precision. _ suite a ces resultats, des calculs lda et gw ont ete menes par l'equipe du professeur s. Louie a berkeley. Les calculs gw (quasi particules), montrent un accord remarquable avec nos resultats. _ les mesures sur les niveaux 2p du si a hv = 108 ev qui representent en principe le volume montrant les structures les plus fines jamais observees sur les niveaux de cur du si. Elles ont permis de montrer par ailleurs : - que la largeur a mi-hauteur de ces raies depend fortement de la preparation de la surface - que la plupart des valeurs donnees dans la litterature pour la duree de vie du trou ainsi que pour la contribution des phonons sont fausses. - que les mesures sur des surfaces differentes (si(111) hydrogene, photodesorbe, si(7x7) montrent clairement que la mesure de la duree de vie du trou par photoemission ne peut etre une technique fiable. _ les mesures de photoemission sur les niveaux de cur a hv = 130 ev (sensibilite a la surface) ont permis d'etudier les deplacements des niveaux de cur a la surface.
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Haug, Kerstin Leigh 1971. "The unique reactions of surface bound H, bulk H, and gas phase H atoms with acetylene, ethylene and ethane on Ni(111)." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/84737.

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Hugelmann, Martin [Verfasser]. "Erzeugung und Charakterisierung metallischer Nanostrukturen auf n-Si(111):H-Einkristalloberflächen / Martin Hugelmann." Karlsruhe : Univ.-Verl. Karlsruhe, 2004. http://d-nb.info/973495839/34.

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Razado-Colambo, Ivy. "Scanning Tunneling Microscopy and Photoelectron Spectroscopy Studies of Si(111) and Ge(111) Surfaces : Clean and Modified by H or Sn Atoms." Doctoral thesis, Linköpings universitet, Tekniska högskolan, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-17371.

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The (111) surfaces of Si and Ge were studied by scanning tunneling microscopy (STM) and photoelectron spectroscopy (PES) that are complementary techniques used to obtain structural and electronic properties of surfaces. The (111) surfaces have been of great interest because of the complex reconstructions formed by annealing. Adsorption of different types of atoms on these surfaces has been widely explored by many research groups. In this thesis work, both clean and modified Si(111) and Ge(111) surfaces were extensively studied to gain information about their atomic and electronic structures. Hydrogen plays a significant role in surface science, specifically in passivating dangling bonds of semiconductor surfaces. There has been a significant number of studies performed on hydrogen exposure of the Si(111)7x7 surface. However, most studies were done after higher exposures resulting in a 1x1 surface. In this thesis work, low hydrogen exposures were employed such that the 7x7 structure was preserved. STM images revealed that the hydrogen atoms preferentially adsorb on the rest atoms at elevated temperatures. A hydrogen terminated rest atom dangling bond is no longer visible in the STM image and the surrounding adatoms become brighter. This implies that there is a charge transfer back to the adatoms. Three types of Htermination (1H, 2H and 3H) were studied in detail by analysing the line profiles of the apparent heights. There are still unresolved issues regarding the electronic structure of the Ge(111)c(2x8) surface. By combining STM, angle-resolved photoelectron spectroscopy (ARPES), and theoretical calculations, new results about the electronic structure of the clean surface have been obtained in this thesis. A more detailed experimental surface band structure showing seven surface state bands is presented. A split surface state band in the photoemission data matched a split between two types of rest atom bands in the calculated surface band structure. A highly dispersive band close to the Fermi level was identified with states below the adatom and rest atom layers and is therefore not a pure surface state. The bias dependent STM images which support the photoemission results were in agreement with simulated images generated from the calculated electronic structure of the c(2x8) surface. Many studies have been devoted to hydrogen adsorption on Si(111)7x7 but only a few have dealt with Ge(111)c(2x8). In this work, hydrogen adsorption on Ge(111)c(2x8) has been studied using STM and ARPES. The preferred adsorption site is the rest atom. As a consequence of the adsorption on the rest atom there is a reverse charge transfer to the adatoms, which makes them appear brighter in the filled-state STM images. Photoemission results showed that for the H-exposed surface, the surface states associated with the rest-atom dangling bonds decreased in intensity while a new peak appeared in the close vicinity of the Fermi level which is not present in the spectrum of the clean surface. This is a clear evidence of a semiconducting to metallic transition of the Ge(111)c(2x8) surface. A higher H exposure on the Ge(111)c(2x8) surface was also done which resulted in a 1x1 surface. The electronic structure was investigated using ARPES. Two surface states were observed that are related to the Ge-Ge backbonds and the Ge-H bonds. Sn/Ge(111) has attracted a lot of attention from the surface science community because of the interesting phase transition from the RT-(√3x√3) phase to the LT-(3x3) phase. Previously, the Sn/Ge(111)√3x√3 surface was considered to be just a simple α- phase surface on which the Sn atoms sit on the T4 sites. However, a core-level study of the RT-(√3x√3) surface showed two components in the Sn 4d core-level spectra which implies that there are two inequivalent Sn atoms. The transition was later on explained by the dynamical fluctuation model. There have been different models proposed for the Sn/Ge(111)3x3 structure such as the 2U1D, 1U2D and IDA models. In this thesis work, the surface was studied using STM. The optimum √3x√3 surface was determined by performing different sample preparations. The LT STM images of the 3x3 surface were investigated and they showed that there are different types of Sn atoms such as up and down atoms. A histogram of the apparent height distribution revealed two peaks, a sharper peak associated with the up atoms and a broader peak for the down atoms. The height distribution was used to produce simulated Sn 4d core-level spectra and the line shape was compared to that of experimental spectra.
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Zahl, Percy. "Oberflächenspannung auf Si(111): Heteroepitaxie von Ge und CaF2, Adsorption von H und Sb." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=961158336.

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Zheng, Chaozhi. "Coverage, step and quantum effects on surface diffusion of H on Pt(111) surfaces /." View abstract or full-text, 2004. http://library.ust.hk/cgi/db/thesis.pl?PHYS%202004%20ZHENG.

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Wickard, Todd DeVere. "The First Attachment and Post-Functionalization of Polybutadiene and Thio-Click Functionalized Polybutadiene on H-Terminated Si(111)." BYU ScholarsArchive, 2009. https://scholarsarchive.byu.edu/etd/2035.

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I report the attachment of polymers with pendant vinyl groups to hydrogen-terminated silicon(111) (Si(111)-H) under mild conditions. 1,2-addition polybutadiene (Mw 3200-3500) was attached to Si(111)-H at room temperature with visible light. I also report the partial functionalization, in solution, of 1,2-addition polybutadiene with various thiols using thiol-click chemistry. These compounds bind to Si(111)-H via visible light activation. The partially functionalized polybutadienes allow further functionalization at the surface through unreacted carbon-carbon double bonds. Surfaces were characterized with contact angle goniometry, spectroscopic ellipsometry, X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and atomic force microscopy (AFM).
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Books on the topic "H-111"

1

Malherbe, Charles, ed. La Damnation de Faust, Op. 24 / H. 111: Vocal score. Edwardsville: Serenissima Music, 2009.

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United States. Congress. House. Committee on Rules. Providing for the consideration of H.R. 2: Report (to accompany H. Res. 111). [Washington, D.C.?: U.S. G.P.O., 1989.

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United States. Congress. House. Committee on Rules. Providing for the consideration of H.R. 1175: Report (to accompany H. Res. 111). [Washington, D.C.?: U.S. G.P.O., 1991.

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United States. Congress. House. Committee on Rules. Providing for the consideration of H.R. 2: Report (to accompany H. Res. 111). [Washington, D.C.?: U.S. G.P.O., 1989.

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Bergeld, Johan. Thermo- and photostimulated reactions of H₂O, O₂, and CO on Pt(111) and C(0001) surfaces. Göteborg: Göteborg University, Department of Physics, 2007.

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Rules, United States Congress House Committee on. Providing for the consideration of H.J. Res. 111, tax limitation constitutional amendment: Report (to accompany H. Res. 407). [Washington, D.C: U.S. G.P.O., 1998.

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United States. Congress. House. Committee on Rules. Providing for the consideration of H.J. Res. 111, tax limitation constitutional amendment: Report (to accompany H. Res. 407). [Washington, D.C: U.S. G.P.O., 1998.

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United States. Congress. House. Committee on Rules. Providing for consideration of H.R. 8, Death Tax Elimination Act of 2001: Report (to accompany H. Res. 111). Washington, D.C.]: [U.S. G.P.O.], 2001.

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United States. Congress. House. Committee on Rules. Providing for consideration of House Joint Resolution 111, making continuing appropriations for the fiscal year 2003: Report (to accompany H. Res. 550). Washington, D.C.]: [U.S. G.P.O.], 2002.

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United States. Congress. House. Committee on Foreign Affairs. Consideration of miscellaneous bills and resolutions: Full committee markup before the Committee on Foreign Affairs, House of Representatives, One Hundred Third Congress, second session, on H. Res. 323, H. Con. Res. 180, H. Con. Res. 124, H.R. 3813, H.R. 4429, H. Con. Res. 111, H.R. 4635, H.J. Res. 388, H. Res. 476, H. Res. 471, H. Con. Res. 151, H.R. 2826, S.J. Res. 204, proposed legislative language to implement the Uruguay Round, H. Con. Res. 250, H.R. 5030, H.R. 5034, H.R. 4541, H. Con. Res. 257, H.R. 4950, H.R. 5108, H. Con. Res. 286, H. Con. Res. 279, H.R. 5155, H. Con. Res. 302, H. Res. 561, S. Con. Res. 74, H. Con. Res. 216, H. Con. Res. 278, and H. Res. 560, January 25, February 9, March 16, May 18, June 23, July 19, August 3, September 13 and 28, and October 3, 1994. Washington: U.S. G.P.O., 1994.

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Book chapters on the topic "H-111"

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Guyot-Sionnest, P., P. Dumas, Y. J. Chabal, and G. S. Higashi. "Lifetime of an Adsorbate Substrate Vibration: H on Si(111)." In Springer Series in Chemical Physics, 374–76. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84269-6_114.

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Rosenberg, R. A., C. R. Wen, and D. C. Mancini. "Temperature-Dependent PSD of H+ from H2O/Si(111) (7×7)." In Desorption Induced by Electronic Transitions DIET III, 220–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73728-2_31.

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Jackson, B., and M. Persson. "Eley-Rideal Dynamics of the Reaction of Gas-Phase H(D) with D(H) on Cu(111)." In Springer Series in Solid-State Sciences, 26–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61185-8_2.

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Harder, R., G. Herrmann, J. H. Rechtien, and K. J. Snowdon. "Orientation Effects in the Scattering of H2 and H+ 2 from Cu(111)." In Springer Series in Surface Sciences, 125–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78080-6_19.

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Brown, N. F., and M. A. Barteau. "Activation of C-H, C-C, and C-O Bonds of Oxygenates on Rh(111)." In ACS Symposium Series, 345–54. Washington, DC: American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0517.ch024.

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Thompson, Noel. "Conclusions." In G. D. H. Cole: Selected Works, 2257–70. London: Routledge, 2022. http://dx.doi.org/10.4324/9780203839317-111.

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Sahu, D., S. C. Ying, and J. M. Kosterlitz. "Theory of Phase Transitions on H/W(110) and H/Mo(110) Systems." In Springer Series in Surface Sciences, 470–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73343-7_77.

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Jaccob, Madhavan, Gopalan Rajaraman, and Federico Totti. "On the kinetics and thermodynamics of S–X (X = H, CH3, SCH3, COCH3, and CN) cleavage in the formation of self-assembled monolayers of alkylthiols on Au(111)." In Vincenzo Barone, 99–109. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-34462-6_10.

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Behm, R. J., K. Christmann, C. Ertl, V. Penka, and R. Schwankner. "Competing Reconstruction Mechanisms in H/Ni(110)." In The Structure of Surfaces, 257–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-82493-7_41.

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Simon, Helmut, Helmut Günther, Johann Bader, and Stefan Neumann. "Chiral Products from Non-Pyridine Nucleotide-Dependent Reductases and Methods for NAD(P)H Regeneration." In Ciba Foundation Symposium 111 - Enzymes in Organic Synthesis, 97–111. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720929.ch8.

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Conference papers on the topic "H-111"

1

Guyot-Sionnest, P., P. Dumas, Y. J. Chabal, and G. S. Higashi. "Lifetime of an Adsorbate-Substrate Vibration: H on Si(111)." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/up.1990.wd5.

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Among the recent developments in surface science is the study of dynamical processes and energy transfers. It is thought in particular that lifetimes of adsorbate vibrations should have an important effect on the chemistry of adsorbates on surfaces.
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Billing, G. D., and M. Cacciatore. "Recombination coefficient and final state vibrational distribution for the reaction: H+Had+Cu(111)→H2(v)+Cu(111)." In Joint meeting of the seventh international symposium on the production and neutralization of negative ions and beams and the sixth European workshop on the production and applicaton of light negative ions. AIP, 1996. http://dx.doi.org/10.1063/1.51281.

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Dogan Vurdu, Can, Muhammet Serdar Cavus, and Fatma Kandemirli. "Investigation of H(2H) - Pt(111) Interaction System: using Density Functional Methods." In 3rd International Conference on Computation for Science and Technology (ICCST-3). Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/iccst-15.2015.28.

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Guyot-Sionnest, Philippe. "Nonlinear optical probes of surface dynamics: application to the vibrational dynamics of Si-H for Si(111)/H." In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, edited by Cheuk Yiu Ng. SPIE, 1993. http://dx.doi.org/10.1117/12.143099.

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Miyauchi, Y., H. Sano, and G. Mizutani. "Images of hydrogen deficiency on H-Si (111) surfaces observed by second harmonic microscopy." In Nonlinear Optics: Materials, Fundamentals and Applications. Washington, D.C.: OSA, 2004. http://dx.doi.org/10.1364/nlo.2004.wd15.

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Miyauchi, Yoshihiro, Khuat Thi Thu Hien, and Goro Mizutani. "Modulation of Si-H vibrational mode as a function of the hydrogen coverage on a H-Si(111)1×1 surface." In International Conference on Photonics Solutions 2013, edited by Prathan Buranasiri and Sarun Sumriddetchkajorn. SPIE, 2013. http://dx.doi.org/10.1117/12.2021685.

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Höfer, U., T. F. Heinz, Leping Li, and G. A. Reider. "Nonlinear optical studies of adsorbates on silicon surfaces." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.tuss2.

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Second-harmonic generation (SHG) provides a sensitive probe of the dynamics of adsorption on semiconductor surfaces. The technique has been applied to examine diffusion, desorption, and dissociation processes on silicon surfaces. Desorption has been investigated for hydrogen on Si(111)7×7 and Si(100)2×1 through isothermal measurements. The high sensitivity of SHG to adsorbed hydrogen allows us to perform such experiments at coverages well below 1% of a monolayer. For both surfaces, the results reveal a marked departure from the second-order kinetics expected for a recombinative desorption reaction. This observation is related to the details of the surface structure. Surface diffusion has been investigated by means of second-harmonic diffraction from a spatially modulated adsorbate density. For H/ Si(111)7×7, a diffusion barrier of 1.5 eV, ~50% of the H-Si binding energy, has been established. Such a high barrier for lateral motion stands in marked contrast to the usual behavior on metal surfaces. For NH3 and O2 on Si(111), SHG is found to be strongly dependent on the chemical state of these adsorbates, permitting real-time investigations of dissociation reactions.
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Voss, M. R. "Atomic H(D) adsorption on polycrystalline UO[sub 2] and UO[sub 2](111) surfaces." In Plutonium futures-The science (Topical conference on Plutonium and actinides). AIP, 2000. http://dx.doi.org/10.1063/1.1292322.

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Gokce, Bilal, Eric J. Adles, David E. Aspnes, Kenan Gundogdu, Jisoon Ihm, and Hyeonsik Cheong. "Measurement and Control of In-Plane Surface Chemistry During Oxidation of H-Terminated (111)Si." In PHYSICS OF SEMICONDUCTORS: 30th International Conference on the Physics of Semiconductors. AIP, 2011. http://dx.doi.org/10.1063/1.3666321.

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Tsuge, K., Y. Jingu, H. Umezawa, and H. Kawarada. "High hole current density in diamond MOSFETs fabricated on H-terminated Iia-type (111) diamond substrate." In 2009 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2009. http://dx.doi.org/10.7567/ssdm.2009.k-5-1.

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Reports on the topic "H-111"

1

Chan, Tzu-Liang. Theoretical Studies of Pb on Si(111) and Si(100), Global Search for H-Passivated Si Nanowires, and Construction of highly Localized Quasiatomic Minimal Basis Orbitals for Mo. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/861606.

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J.D. Ludowise. Final Hazard Categorization for the Remediation of the 118-D-1, 118-D-2, 118-D-3, 118-H-1, 118-H-2, and 118-H-3 Solid Waste Burial Grounds. Office of Scientific and Technical Information (OSTI), June 2009. http://dx.doi.org/10.2172/972717.

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T. J. Rodovsky. Final Hazard Categorization for the Remediation of the 118-D-1, 118-D-2, 118-D-3, 118-H-1, 118-H-2, and 118-H-3 Solid Waste Burial Grounds. Office of Scientific and Technical Information (OSTI), April 2007. http://dx.doi.org/10.2172/944090.

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T. J. Rodovsky. Final Hazard Categorization for the Remediation of the 118-D-1, 118-D-2, 118-D-3, 118-H-1, 118-H-2, and 118-H-3 Solid Waste Burial Grounds. Office of Scientific and Technical Information (OSTI), December 2006. http://dx.doi.org/10.2172/944091.

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K. L. Vialetti. Final Hazard Categorization for the Remediation of the 118-D-1, 118-D-2, 118-D-3, 118-H-1, 118-H-2 and 118-H-3 Solid Waste Burial Grounds. Office of Scientific and Technical Information (OSTI), May 2008. http://dx.doi.org/10.2172/945404.

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T. J. Rodovsky. Final Hazard Categorization and Auditable Safety Analysis for the Remediation of the 118-D-1, 118-D-2, 118-D-3, 118-H-1, 118-H-2 and 118-H-3 Solid Waste Burial Grounds. Office of Scientific and Technical Information (OSTI), March 2006. http://dx.doi.org/10.2172/945400.

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Kiss, F. Residual total magnetic field, Kluane area aeromagnetic survey, parts of NTS 115 G/8, 115 H/5 and 115 H/6, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2010. http://dx.doi.org/10.4095/286072.

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Kiss, F. Residual total magnetic field, Kluane area aeromagnetic survey, NTS 115 H/4 and parts of 115 H/3 and 115 G/1, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2010. http://dx.doi.org/10.4095/286070.

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Kiss, F. Residual total magnetic field, Kluane area aeromagnetic survey, parts of NTS 115 H/11 and 115 H/12, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2010. http://dx.doi.org/10.4095/286074.

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Kiss, F. First vertical derivative of the magnetic field, Kluane area aeromagnetic survey, parts of NTS 115 G/8, 115 H/5 and 115 H/6, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2010. http://dx.doi.org/10.4095/286073.

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