Relevant bibliographies by topics / Amorphous carbon materials

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Amorphous carbon materials'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Amorphous carbon materials"

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Robertson, J. "π-bonded clusters in amorphous carbon materials". Philosophical Magazine B 66, № 2 (1992): 199–209. http://dx.doi.org/10.1080/13642819208224583.

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Rodil, S. E. "Infrared spectra of amorphous carbon based materials." Diamond and Related Materials 14, no. 8 (2005): 1262–69. http://dx.doi.org/10.1016/j.diamond.2005.01.044.

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Blanco, A., A. Borghesi, V. Orofino, et al. "Amorphous carbon and carbonaceous materials in space." Il Nuovo Cimento C 13, no. 1 (1990): 231–39. http://dx.doi.org/10.1007/bf02515792.

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Blanco, A., A. Borghesi, V. Orofino, et al. "Amorphous carbon and carbonaceous materials in space." Il Nuovo Cimento C 13, no. 1 (1990): 241–47. http://dx.doi.org/10.1007/bf02515793.

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Sullivan, J. P., T. A. Friedmann, and K. Hjort. "Diamond and Amorphous Carbon MEMS." MRS Bulletin 26, no. 4 (2001): 309–11. http://dx.doi.org/10.1557/mrs2001.68.

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The designer of microelectromechanical systems (MEMS) can increase MEMS performance either by improved mechanical design or by the selection of a MEMS material with improved mechanical performance. In the quest to identify highperformance MEMS materials, diamond and amorphous carbon have recently emerged as a promising class of materials.
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Muller, David A. "Electron-diffraction studies of amorphous carbon thin films." Proceedings, annual meeting, Electron Microscopy Society of America 51 (August 1, 1993): 1100–1101. http://dx.doi.org/10.1017/s0424820100151337.

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The sp2 rich amorphous carbons have a wide variety of microstructures ranging from flat sheetlike structures such as glassy carbon to highly curved materials having similar local ordering to the fullerenes. These differences are most apparent in the region of the graphite (0002) reflection of the energy filtered diffracted intensity obtained from these materials (Fig. 1). All these materials consist mainly of threefold coordinated atoms. This accounts for their similar appearance above 0.8 Å-1. The fullerene curves (b,c) show a string of peaks at distance scales corresponding to the packing of the large spherical and oblate molecules. The beam damaged C60 (c) shows an evolution to the sp2 amorphous carbons as the spherical structure is destroyed although the (220) reflection in fee fcc at 0.2 Å-1 does not disappear completely. This 0.2 Å-1 peak is present in the 1960 data of Kakinoki et. al. who grew films in a carbon arc under conditions similar to those needed to form fullerene rich soots.
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Jiang, Yun, Hong Wen Ma, and Yu Qin Liu. "Experimental Study on Carbothermic Reduction of Magnesia with Different Carbon Materials." Advanced Materials Research 652-654 (January 2013): 2552–55. http://dx.doi.org/10.4028/www.scientific.net/amr.652-654.2552.

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The structure and composition of carbon materials affect obviously the result of carbothermic reduction of magnesia. Coke, charcoal and graphite were used in reduction experiments under the same conditions. The reactivity ratio of magnesia and XRD pattern of residues were analyzed and compared. The reactivity ratio of magnesia by coke was similar to the one by charcoal. The amorphous carbon in coke graphitized partly in reduction experiments of 1673K. The results show that the effective composition in coke is the amorphous carbon. It also suggests that the temperature of reaction should be control less than 1700K to avoid the amorphous carbon’s graphitization.
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Logothetidis, S. "Optical and electronic properties of amorphous carbon materials." Diamond and Related Materials 12, no. 2 (2003): 141–50. http://dx.doi.org/10.1016/s0925-9635(03)00015-3.

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Chae, Ji Su, Won-seop Kang, and Kwang Chul Roh. "sp2–sp3 Hybrid Porous Carbon Materials Applied for Supercapacitors." Energies 14, no. 19 (2021): 5990. http://dx.doi.org/10.3390/en14195990.

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Carbon materials have gained considerable attention in recent years due to their superior properties. Activated carbon has been used in supercapacitors due to its density and rapid adsorption capability. The sp2–sp3 hybrid porous carbon materials are synthesized using herringbone-type carbon nanofibers (CNFs) and carbonized spherical phenol resins, with KOH as the activating agent. The morphology of the hybrid porous carbon facilitates the formation of ribbon-like nanosheets from highly activated CNFs wrapped around spherical resin-based activated carbon. The etching and separation of the CNFs produce a thin ribbon-like nanosheet structure; these CNFs simultaneously form new bonds with activated carbon, forming the sp2–sp3 hybrid porous structure. The relatively poor electrical conductivity of amorphous carbon is improved by the 3D conductive network that interconnects the CNF and amorphous carbon without requiring additional conductive material. The composite electrode has high electron conductivity and a large surface area with a specific capacitance of 120 F g−1. Thus, the strategy substantially simplifies the hybrid materials of sp2-hybridized CNFs and sp3-hybridized amorphous spherical carbon and significantly improves the comprehensive electrochemical performance of supercapacitors. The developed synthesis strategy provides important insights into the design and fabrication of carbon nanostructures that can be potentially applied as electrode materials for supercapacitors.
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Boychuk, V. M., L. O. Shyyko, V. O. Kotsyubynsky, and A. Kachmar. "Structure and morphology of MoS2 / Carbon nanocomposite materials." Фізика і хімія твердого тіла 20, no. 1 (2019): 63–68. http://dx.doi.org/10.15330/pcss.20.1.68.

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The paper presents the experimental results of the hydrothermal synthesis composite materials based on the MoS2 and carbon using different types of detergents (cetyltrimethylammonium bromide and Triton-X) or microporous carbon. The synthesized material was studied by XRD, TEM, and EDS. The investigation of structural and morphological properties of the obtained nanocomposite material shows that the nanoparticles (the average size of about 40 nm) obtained by detergent-assisted procedure have a multilayer crystal ordered superficial layers where quasi-two-dimensional MoS2 layers alternate with amorphous carbon. The annealing at 500oC in argon caused the formation turbostratically stacked layers of crystalline MoS2 with amorphous carbon located in the interlayer space. The core-shall morphology (carbon nanoparticles on the surface of MoS2 clusters) was observed for composite materials synthesized on the base of microporous carbon.
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Dissertations / Theses on the topic "Amorphous carbon materials"

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Dawson, Janet Caroline. "The electronic properties of granular and amorphous materials." Thesis, University of Cambridge, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318097.

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Li, Yuting. "Simulations and Electronic Structure of Disordered Silicon and Carbon Materials." Ohio University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395410498.

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Burke, Theresa Mary. "An X-ray and neutron scattering study of amorphous hydrogenated carbon." Thesis, University of Kent, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240132.

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Lau, Desmond, and desmond lau@rmit edu au. "Characterisation of Novel Carbonaceous Materials Synthesised Using Plasmas." RMIT University. Applied Sciences, 2009. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20091119.102551.

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Novel carbon materials such as carbon onions, nanotubes and amorphous carbon (a-C) are technologically important due to their useful properties. Normally synthesised using plasmas, their growth mechanisms are not yet fully understood. For example, the growth mechanism of the high density phase of a-C, tetrahedral amorphous carbon (ta-C), has been a subject of debate ever since its discovery. The growth mechanism of carbon nanostructures such as carbon onions and nanotubes is also not well known. The aim of this thesis is two-fold. Firstly, to provide insight into the growth of carbon films, in particular, the driving force behind the formation of diamond-like bonding in a-C which leads to ta-C. Secondly, to investigate the growth of carbon onions and other sp2 bonded carbon nanostructures such as nanotubes. To achieve the first aim, carbon thin films were deposited using cathodic arc deposition at a range of ion energies, substrate temperatures and Ar background gas pressures. These films were characterised using electron microscopy techniques to examine their microstructure, density and sp3 content. It was found that the formation of the ta-C is due to a stress-induced transition whereby a critical stress of 6.5±1.5 GPa is needed to change the phase of the film from highly sp2 to highly sp3. Within this region, a preferentially oriented phase with graphitic sheets aligned perpendicular to the substrate surface was found. By investigating the role of elevated temperatures, the ion energy-temperature
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Gammon, W. Jason. "Chemical bonding in hard and elastic amorphous carbon-nitride films." W&M ScholarWorks, 2003. https://scholarworks.wm.edu/etd/1539623423.

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In this study, the chemical bonding in hard and elastic amorphous carbon nitride (a-CNx) films is investigated with x-ray photoelectron spectroscopy (XPS) and 15N, 13C, and 1H nuclear magnetic resonance (NMR) spectroscopy. The films were deposited by DC Magnetron sputtering in a pure nitrogen discharge on Si(001) substrates at 300--400??C. Nanoindentation measurements reveal an elastic modulus of ∼50 GPa and a hardness of ∼5 GPa, thus confirming our films are highly elastic but resist plastic deformation.;Our 13C NMR study demonstrates the absence of sp 3-bonded carbon in this material. Collectively, our N(1s) XPS, 13C NMR, and 15N NMR data suggest a film-bonding model that has an aromatic carbon structure with sp2-hybridized nitrogen incorporated in heterocyclic rings. We demonstrate that the nitrogen bonding is predominantly in configurations similar to those in pyridine and pyrrole. In addition, the data indicate that the a-CNx films prepared for this study have low hydrogen content, but are hydrophilic. Specifically, results from 15N and 13C cross polarization (CP) and 1H magic angle spinning (MAS) NMR experiments suggest that nitrogen sites are susceptible to protonation from water absorbed during sample preparation for the NMR experiments. The sensitivity of the surface of a-CNx to water absorption may impact tribological applications for this material.;In accord with our XPS and NMR spectroscopic studies on a-CN x films, we propose a film-structure model consisting of buckled graphitic planes that are cross-linked together by sp2 hybridized carbons. The curvature and cross-linking is attributed to a type of compound defect, which is formed by placing a pentagon next to single-atom vacancy in a graphite layer. Our proposed film structure is called the pentagon-with-vacancy-defect (5VD) model. Using Hartree-Fock calculations, we show that the 5VD, film-structure model is compatible with our XPS, NMR, and nanoindentation measurements and with previous transmission electron microscopy (TEM) and computational work.
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Merchant, Alexander Raymond. "An investigation of carbon nitride." University of Sydney. Physics, 2001. http://hdl.handle.net/2123/832.

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This thesis employs experimental and theoretical methods to characterise carbon nitride solids and proposes a generalstructural model for amorphous carbon nitride (a-C:N). It finds that a-C:N deposited by several methods is essentially identical, with similar bonding environments for carbon and nitrogen atoms. Using evidence from several techniques, the saturation of nitrogen in an sp2 carbon matrix is discussed. The experimental studies on a range of carbon nitride solids show no evidence for a crystalline form of carbon nitride. In addition to the experimental characterisation of a-C:N, ab initio molecular dynamics were used to investigate bonding and structure in carbon nitride. These simulations show that the most common form of nitrogen bonding was three-fold sites with a lone pair of electrons. Two-fold nitrogen sites were also found in agreement with experimental findings. An increase of nitrogen in a-C:N decreases the sp3-carbon fraction, but this is not localised on the nitrogen and the effect is most severe at high densities. A simulation of a low density/high nitrogen content network shows that the nitrogen saturation seen experimentally may be due to the formation of N2 dimers and C-N molecules which are easily driven out of the structure. The ab initio simulations also explore the nature of charged nitrogen and carbon sites in a-C:N. An analysis based on Wannier Function centres provided further information about the bonding and allowed for a detailed classification of these sites. The removal of electrons from the networks caused structural changes that could explain the two-state conductivity in ta-C:N memory devices. Finally, a theoretical study of the electron energy-loss near-edge structure (ELNES) calculated using multiple scattering theory is presented. The calculated ELNES of diamond, graphite and boron, silicon and carbon nitride structures compare well to experiment and supports the experimental finding that no crystalline carbon nitride had (or has) been produced. These ELNES calculations will however, provide a means of identifying crystalline beta-C3N4 should it be synthesised.
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Prasai, Kiran. "Gap Engineering and Simulation of Advanced Materials." Ohio University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1503393620371266.

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Forrest, Roy Duncan. "Electron field emission from amorphous semiconductor thin films." Thesis, University of Surrey, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.484237.

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Brown, James Emery. "Advances in electrical energy storage using core-shell structures and relaxor-ferroelectric materials." Diss., Kansas State University, 2018. http://hdl.handle.net/2097/38779.

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Doctor of Philosophy
Department of Chemistry
Jun Li
Electrical energy storage (EES) is crucial in todays’ society owing to the advances in electric cars, microelectronics, portable electronics and grid storage backup for renewable energy utilization. Lithium ion batteries (LIBs) have dominated the EES market owing to their wide use in portable electronics. Despite the success, low specific capacity and low power rates still need to be addressed to meet the increasing demands. Particularly, the low specific capacity of cathode materials is currently limiting the energy storage capability of LIBs. Vanadium pentoxide (V₂O₅) has been an emerging cathode material owing to its low cost, high electrode potential in lithium-extracted state (up to 4.0 V), and high specific capacities of 294 mAh g⁻¹ (for a 2 Li⁺/V₂O₅ insertion process) and 441 mAh g⁻¹ (for a 3 Li⁺/V₂O₅ insertion process). However, the low electrical conductivities and slow Li⁺ ion diffusion still limit the power rate of V₂O₅. To enhance the power-rate capability we construct two core-shell structures that can achieve stable 2 and 3 Li⁺ insertion at high rates. In the first approach, uniform coaxial V₂O₅ shells are coated onto electrospun carbon nanofiber (CNF) cores via pulsed electrodeposition. The materials analyses confirm that the V₂O₅ shell after 4 hours of thermal annealing at 300 °C is a partially hydrated amorphous structure. SEM and TEM images indicate that the uniform 30 to 50 nm thick V₂O₅ shell forms an intimate interface with the CNF core. Lithium insertion capacities up to 291 and 429 mAh g⁻¹ are achieved in the voltage ranges of 4.0 – 2.0 V and 4.0 – 1.5 V, respectively, which are in good agreement with the theoretical values for 2 and 3 Li⁺/V₂O₅ insertion. Moreover, after 100 cycles, remarkable retention rates of 97% and 70% are obtained for 2 and 3 Li⁺/V₂O₅ insertion, respectively. In the second approach, we implement a three-dimensional (3D) core-shell structure consisting of coaxial V₂O₅ shells sputter-coated on vertically aligned carbon nanofiber (VACNF) cores. The hydrated amorphous microporous structure in the “as-deposited” V₂O₅ shells and the particulated nano-crystalline V₂O₅ structure formed by thermal annealing are compared. The former provides remarkably high capacity of 360 and 547 mAh g⁻¹ in the voltage range of 4.0 – 2.0 V and 4.0 – 1.5 V, respectively, far exceeding the theoretical values for 2 and 3 Li⁺/V₂O₅ insertion, respectively. After 100 cycles of 3 Li⁺/V₂O₅ insertion/extraction at 0.20 A g⁻¹ (~ C/3), ~ 84% of the initial capacity is retained. After thermal annealing, the core-shell structure presents a capacity of 294 and 390 mAh g⁻¹, matching well with the theoretical values for 2 and 3 Li⁺/V₂O₅ insertion. The annealed sample shows further improved stability, with remarkable capacity retention of ~100% and ~88% for 2 and 3 Li⁺/V₂O₅ insertion/extraction. However, due to the high cost of Li. alternative approaches are currently being pursued for large scale production. Sodium ion batteries (SIB) have been at the forefront of this endeavor. Here we investigate the sodium insertion in the hydrate amorphous V₂O₅ using the VACNF core-shell structure. Electrochemical characterization was carried out in the potential ranges of 3.5 – 1.0, 4.0 – 1.5, and 4.0 – 1.0 (vs Na/Na⁺). An insertion capacity of 196 mAh g-1 is achieved in the potential range of 3.5 – 1.0 V (vs Na/Na⁺) at a rate of 250 mA g⁻¹. When the potential window is shifted upwards to 4.0 – 1.5 V (vs Na/Na⁺) an insertion capacity of 145 mAh g⁻¹ is achieved. Moreover, a coulombic efficiency of ~98% is attained at a rate of 1500 mA g⁻¹. To enhance the energy density of the VACNF-V₂O₅ core-shell structures, the potential window is expanded to 4.0 – 1.0 V (vs Na/Na⁺) which achieved an initial insertion capacity of 277 mAh g⁻¹. The results demonstrate that amorphous V₂O₅ could serve as a cathode material in future SIBs.
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Maddi, Chiranjeevi. "Laser technologies for the development of carbon materials for environmental analytical microsystems." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSES014/document.

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Technologies laser pour l’élaboration de matériaux carbonés pour microsystèmes analytiques environnementaux. Pas de résumé en français fourni
Amorphous carbon nitride (a-CzN) material has attractor much attention in research and development. Recently, it has become a more promising electrode material than conventional carbon based electrodes in electrochemical and biosensor applications. Nitrogen containing amorphous carbon (a-C:N) thin films have been synthesized by femtosecond pulsed laser deposition (fs-PLD) coupled with plasma assistance through Direct Current (DC) bias power supply. During the deposition process, various nitrogen pressures (0 to 50 Pa) and DC bias (0 to -350 V) were used in order to explore a wide range of nitrogen content into the film. The structure and chemical composition of the films have been studied by using Multi-wavelength (MW) Roman spectroscopy, electron energy-loss spectroscopy (EELS), X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTBM). The surface morphology has been studied by Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). Increasing the nitrogen pressure or adding a DC bias induced an increase of the N content, up to 28 at.%. Nitrogen content increase induces a higher sp2 character of the film. However DC bias has been found to increase the film structmal disorder, which was detrimental to the electrochemical properties. Indeed the electrochemical measurern-ts, investigated by cyclic voltammetry (CV), demonstrated that the a-CzNfilms show better electron transfer kinetics, reversibility and excellent reproducibility than the pure a-C films. Electrochemical grafting from diazoniurn salts was successfully achieved on this film, with a surface coverage of covalently bonded molecules close to the dense packed monolayer of ferrocene
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Books on the topic "Amorphous carbon materials"

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Pouch, John J. Auger electron spetroscopy, secondary ion mass spectrometry and optical characterization of a-C:H and BN films. National Aeronautics and Space Administration, Lewis Research Center, 1986.

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Robertson, J., O. Zhou, T. B. Allen, B. F. Coll, and J. P. Sullivan. Amorphous and Nanostructured Carbon: Volume 593. University of Cambridge ESOL Examinations, 2014.

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Koidl, P. Amorphous Hydrogenated Carbon Films, 1987 (Symposia proceedings / European Materials Research Society). Materials Research Society, 1987.

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Pouch, John J. Properties and Characterization of Amorphous Carbon Films (Materials Science Forum, Vol 52-53). Trans Tech Publications, 1990.

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P, Sullivan J., ed. Amorphous and nanostructured carbon: Symposium held November 29-December 2, 1999, Boston, Massachusetts, U.S.A. Materials Research Society, 2000.

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(Editor), John P. Sullivan, John Robertson (Editor), Otto Zhou (Editor), Tatiana B. Allen (Editor), and Bernard F. Coll (Editor), eds. Amorphous and Nanostructured Carbon: Symposium Held November 29-December 2, 1999,Boston, Massachusetts, U.S.A (Materials Research Society Symposium Proceedings). Materials Research Society, 2000.

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Book chapters on the topic "Amorphous carbon materials"

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Bakar, Suriani Abu, Azira Abdul Aziz, Putut Marwoto, Samsudi Sakrani, Roslan Md Nor, and Mohamad Rusop. "Hydrogenated Amorphous Carbon Films." In Advanced Structured Materials. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/8611_2010_15.

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Martinu, Ludvik. "Amorphous Carbon Films." In High Energy Density Technologies in Materials Science. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0499-6_6.

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Marks, Nigel A. "Amorphous Carbon and Related Materials." In Computer-Based Modeling of Novel Carbon Systems and Their Properties. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-1-4020-9718-8_5.

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Aono, Masami, and Tomo Harata. "Photomechanical Response of Amorphous Carbon Nitride Thin Films and Their Applications in Light-Driven Pumps." In Carbon Related Materials. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-7610-2_13.

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Galli, Giulia, Richard M. Martin, Roberto Car, and Michele Parrinello. "Ab-Initio Study of Amorphous and Liquid Carbon." In Atomistic Simulation of Materials. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5703-2_17.

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Zheng, Chuan Lin, Wu Bao Yang, and X. Chang. "FCVA-Synthesized Tetrahedral Amorphous Carbon Films for Biomedical Applications." In Key Engineering Materials. Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-410-3.1577.

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Tóth, Sara, M. Füle, M. Veres, I. Pócsik, and Margit Koós. "Supercapacitor Electrodes Made from Mixture of Amorphous Carbon Nano-Particles and Carbon Black." In Materials Science Forum. Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-426-x.263.

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Milne, W. I. "Preparation and Structural Properties of Tetrahedrally Bonded Amorphous Carbon." In Properties and Applications of Amorphous Materials. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0914-0_20.

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Milne, W. I. "Mechanical, Optical and Electrical Properties of Tetrahedrally Bonded Amorphous Carbon." In Properties and Applications of Amorphous Materials. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0914-0_21.

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Milne, W. I. "Field Emission from Carbon Films Grown by the Cathodic Arc Process." In Properties and Applications of Amorphous Materials. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0914-0_22.

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Conference papers on the topic "Amorphous carbon materials"

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Ali, Mokhtar, G. Venkata Ramana, Balaji Padya, V. V. S. S. Srikanth, and P. K. Jain. "Synthesis of amorphous carbon nanofibers using iron nanoparticles as catalysts." In CARBON MATERIALS 2012 (CCM12): Carbon Materials for Energy Harvesting, Environment, Nanoscience and Technology. AIP, 2013. http://dx.doi.org/10.1063/1.4810064.

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Bhattacharyya, Somnath, Swapan K. Pati, and S. V. Subramanyam. "Structural modeling of amorphous conducting carbon film." In Smart Materials, Structures and MEMS, edited by Vasu K. Aatre, Vijay K. Varadan, and Vasundara V. Varadan. SPIE, 1998. http://dx.doi.org/10.1117/12.305621.

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Anikeeva, I. V., A. B. Arbuzov, M. V. Trenikhin, and Yu G. Kryazhev. "Formation of carbon-carbon composite materials with nanoglobular carbon particles embedded in amorphous carbon matrix." In 21ST CENTURY: CHEMISTRY TO LIFE. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122941.

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Rusop, M., Mohamad Rusop, Rihanum Yahaya Subban, Norlida Kamarulzaman, and Wong Tin Wui. "Amorphous Carbon Based Solar Cell: Fabrication and Characterization." In INTERNATIONAL CONFERENCE ON ADVANCEMENT OF MATERIALS AND NANOTECHNOLOGY: (ICAMN—2007). AIP, 2010. http://dx.doi.org/10.1063/1.3377850.

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Kaasik, Friedrich, Janno Torop, Indrek Must, et al. "Ionic EAP transducers with amorphous nanoporous carbon electrodes." In SPIE Smart Structures and Materials + Nondestructive Evaluation and Health Monitoring, edited by Yoseph Bar-Cohen. SPIE, 2012. http://dx.doi.org/10.1117/12.915136.

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Kojima, Nobuaki. "Fabrication of C[sub 60]/amorphous carbon superlattice structures." In NANONETWORK MATERIALS: Fullerenes, Nanotubes, and Related Systems. AIP, 2001. http://dx.doi.org/10.1063/1.1420124.

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Guo, Lei, Ying Gao, Yongxian Xu, Renhui Zhang, Loutfy H. Madkour, and Yingchang Yang. "Understanding the corrosion behavior of amorphous multiple-layer carbon coating." In ADVANCES IN MATERIALS, MACHINERY, ELECTRONICS II: Proceedings of the 2nd International Conference on Advances in Materials, Machinery, Electronics (AMME 2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5033573.

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Mohamad, F., N. M. Hanib, U. M. Noor, et al. "Properties of Amorphous Carbon Thin Films for Solar Cell Applications." In INTERNATIONAL CONFERENCE ON ADVANCEMENT OF MATERIALS AND NANOTECHNOLOGY: (ICAMN—2007). AIP, 2010. http://dx.doi.org/10.1063/1.3377800.

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RUSOP, M., S. M. MOMINUZZAMAN, T. SOGA, T. JIMBO, and M. UMENO. "Characterization of phosphorus doped amorphous carbon and construction of n-carbon/p-silicon heterojunction solar cells." In 2002 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2002. http://dx.doi.org/10.7567/ssdm.2002.lp6-2.

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Pamungkas, Diajeng I., Anas Haikal, Malik A. Baqiya, Yoyok Cahyono, and Darminto. "Synthesis of amorphous carbon from bio-products by drying method." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON MATERIALS AND METALLURGICAL ENGINEERING AND TECHNOLOGY (ICOMMET 2017) : Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. Author(s), 2018. http://dx.doi.org/10.1063/1.5030281.

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