Relevant bibliographies by topics / Core shell structured catalyst

Contents

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

Academic literature on the topic 'Core shell structured catalyst'

Author: Grafiati
Published: 14 July 2021
Last updated: 7 February 2022

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Journal articles on the topic "Core shell structured catalyst"

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Wang, Hong, Ying Wang, Xianyou Wang, Peiying He, Lanhua Yi, Wei Yi, and Xue Liu. "Investigation of the Performance ofAucore-Pdshell/C as the Anode Catalyst of Direct Borohydride-Hydrogen Peroxide Fuel Cell." International Journal of Electrochemistry 2011 (2011): 1–7. http://dx.doi.org/10.4061/2011/129182.

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The carbon-supported bimetallic Au-Pd catalyst with core-shell structure is prepared by successive reduction method. The core-shell structure, surface morphology, and electrochemical performances of the catalysts are characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet-visible absorption spectrometry, linear sweep voltammetry, and chronopotentiometry. The results show that the Au-Pd/C catalyst with core-shell structure exhibits much higher catalytic activity for the direct oxidation of NaBH4than pure Au/C catalyst. A direct borohydride-hydrogen peroxide fuel cell, in which the Au-Pd/C with core-shell structure is used as the anode catalyst and the Au/C as the cathode catalyst, shows as high as 68.215 mW cm−2power density.
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Wu, Yan Ni, Hai Fu Guo, Peng Hu, Xiao Peng Xiao, Zhao Wang Xiao, and Shi Jun Liao. "A Comparative Study on Ternary Low-Platinum Catalysts with Various Constructions for Oxygen Reduction and Methanol Oxidation Reactions." Nano 11, no. 07 (July 2016): 1650081. http://dx.doi.org/10.1142/s1793292016500818.

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Three types of ternary low-platinum nanocatalysts, alloy PdPtIr/C, core–shell PdPt@PtIr/C and Pd@PtIr/C, have been prepared, and their catalytic behaviors toward methanol oxidation reaction (MOR)/oxygen reduction reaction (ORR) are comparatively investigated via cyclic voltammetry and chronoamperometry analysis in an acidic medium. Through a two-step colloidal technique, the synthesized core–shell structured catalyst PtPd@PtIr/C with alloy core and alloy shell show the best catalytic activity toward MOR and the best poisoning tolerance. The alloy PdPtIr/C catalyst prepared via a one-step colloidal technique exhibits the best performance toward ORR among the three catalysts. All the three catalysts are characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and other characterization techniques.
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Zhao, Bonan, Zhipeng Dong, Qiyan Wang, Yisong Xu, Nanxia Zhang, Weixing Liu, Fangning Lou, and Yue Wang. "Highly Efficient Mesoporous Core-Shell Structured Ag@SiO2 Nanosphere as an Environmentally Friendly Catalyst for Hydrogenation of Nitrobenzene." Nanomaterials 10, no. 5 (May 3, 2020): 883. http://dx.doi.org/10.3390/nano10050883.

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The size-uniformed mesoporous Ag@SiO2 nanospheres’ catalysts were prepared in one-pot step via reducing AgNO3 by different types of aldehyde, which could control the size of Ag@SiO2 NPs and exhibit excellent catalytic activity for the hydrogenation of nitrobenzene. The results showed that the Ag core size, monitored by different aldehydes with different reducing abilities, together with the ideal monodisperse core-shell mesoporous structure, was quite important to affect its superior catalytic performances. Moreover, the stability of Ag fixed in the core during reaction for 6 h under 2.0 MPa, 140 °C made this type of Ag@SiO2 catalyst separable and environmentally friendly compared with those conventional homogeneous catalysts and metal NPs catalysts. The best catalyst with smaller Ag cores was prepared by strong reducing agents such as CH2O. The conversion of nitrobenzene can reach 99.9%, the selectivity was 100% and the catalyst maintained its activity after several cycles, and thus, it is a useful novel candidate for the production of aniline.
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Kuttiyiel, Kurian A., Kotaro Sasaki, Wei-Fu Chen, Dong Su, and Radoslav R. Adzic. "Core–shell, hollow-structured iridium–nickel nitride nanoparticles for the hydrogen evolution reaction." J. Mater. Chem. A 2, no. 3 (2014): 591–94. http://dx.doi.org/10.1039/c3ta14301e.

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Hong, Wei, Xin Feng, Lianqiao Tan, Aiming Guo, Bing Lu, Jing Li, and Zidong Wei. "Preparation of monodisperse ferrous nanoparticles embedded in carbon aerogels via in situ solid phase polymerization for electrocatalytic oxygen reduction." Nanoscale 12, no. 28 (2020): 15318–24. http://dx.doi.org/10.1039/d0nr01219j.

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Core–shell structured materials constructed by using Fe/Fe3C cores and nitrogen doped carbon shells represent a type of promising non-precious oxygen reduction reaction (ORR) catalyst due to well-established active sites at the interface positions.
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Nan, Haoxiong, Xinlong Tian, Junming Luo, Dai Dang, Rong Chen, Lina Liu, Xiuhua Li, Jianhuang Zeng, and Shijun Liao. "A core–shell Pd1Ru1Ni2@Pt/C catalyst with a ternary alloy core and Pt monolayer: enhanced activity and stability towards the oxygen reduction reaction by the addition of Ni." Journal of Materials Chemistry A 4, no. 3 (2016): 847–55. http://dx.doi.org/10.1039/c5ta07740k.

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Lee, Hyunju, and Doohwan Lee. "Synthesis Chemistry and Properties of Ni Catalysts Fabricated on SiC@Al2O3 Core-Shell Microstructure for Methane Steam Reforming." Catalysts 10, no. 4 (April 2, 2020): 391. http://dx.doi.org/10.3390/catal10040391.

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Heat and mass transport properties of heterogeneous catalysts have significant effects on their overall performance in many industrial chemical reaction processes. In this work, a new catalyst micro-architecture consisting of a highly thermally conductive SiC core with a high-surface-area metal-oxide shell is prepared through a charge-interaction-induced heterogeneous hydrothermal construction of SiC@NiAl-LDH core-shell microstructures. Calcination and reduction of the SiC@NiAl-LDH core-shell results in the formation of Ni nanoparticles (NPs) dispersed on SiC@Al2O3, referred to as Ni/SiC@Al2O3 core-shell catalyst. The Ni/SiC@Al2O3 exhibit petal-like shell morphology consisting of a number of Al2O3 platelets with their planes oriented perpendicular to the surface, which is beneficial for improved mass transfer. For an extended period of methane-stream-reforming reaction, the Ni/SiC@Al2O3 core-shell structure remained stable without any significant degradation at the core/shell interface. However, the catalyst suffered from coking and sintering likely associated with the relatively large Ni particle sizes and the low Al2O3 content. The synthesis procedure and chemistry for construction of supported Ni catalyst on the core-shell microstructure of the highly thermal conductive SiC core, and the morphology-controlled metal-oxide shell, could provide new opportunities for various catalytic reaction processes that require high heat flux and enhanced mass transport.
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Albers, Peter W., Konrad Möbus, Stefan D. Wieland, and Stewart F. Parker. "The fine structure of Pearlman's catalyst." Physical Chemistry Chemical Physics 17, no. 7 (2015): 5274–78. http://dx.doi.org/10.1039/c4cp05681g.

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Chang, Huazhen, Tao Zhang, Hao Dang, Xiaoyin Chen, Yanchen You, Johannes W. Schwank, and Junhua Li. "Fe2O3@SiTi core–shell catalyst for the selective catalytic reduction of NOx with NH3: activity improvement and HCl tolerance." Catalysis Science & Technology 8, no. 13 (2018): 3313–20. http://dx.doi.org/10.1039/c8cy00810h.

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A core–shell structured Fe2O3@SiTi catalyst with a SiTi shell and Fe2O3 core was prepared and used for the selective catalytic reduction (SCR) of NOx with NH3.
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Liu, Lili, Xiaojing Zhou, Yongmei Yan, Jie Zhou, Wenping Zhang, and Xishi Tai. "Bimetallic Gold-Silver Nanoparticles Supported on Zeolitic Imidazolate Framework-8 as Highly Active Heterogenous Catalysts for Selective Oxidation of Benzyl Alcohol into Benzaldehyde." Polymers 10, no. 10 (October 1, 2018): 1089. http://dx.doi.org/10.3390/polym10101089.

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The metal-organic zeolite imidazolate framework-8 (ZIF-8) supported gold-silver bimetallic catalysts with a core-shell structure (Au@Ag/ZIF-8 and Ag@Au/ZIF-8) and cluster structure (AuAg/ZIF-8) were successfully prepared by the deposition-redispersion method. Energy dispersive X-ray spectroscopy (EDS) elemental mapping images displayed that in the Au@Ag/ZIF-8 catalyst, Ag atoms were deposited on an exposed Au surface, and core-shell structured Au@Ag particles with highly dispersed Ag as the shell were formed. Additionally, the XPS investigation at gold 4f levels and silver 3d levels indicated that the Au and Ag particles of Au@Ag/ZIF-8, Ag@Au/ZIF-8, and AuAg/ZIF-8 were in a zero valence state. Among the resultant catalysts obtained in this study, Ag@Au/ZIF-8 catalysts showed the highest catalytic activity for the selective oxidation of benzyl alcohol, followed by AuAg/ZIF-8 and Au@Ag/ZIF-8. The turnover frequency (TOF) values were in the order of Ag@Au/ZIF-8 (28.2 h−1) > AuAg/ZIF-8 (25.0 h−1) > Au@Ag/ZIF-8 (20.0 h−1) at 130 °C within 1 h under 8 bar O2 when using THF as solvent. The catalysts of Au@Ag/ZIF-8 and Ag@Au/ZIF-8 with core–shell structures have higher benzaldehyde selectivities (53.0% and 53.3%) than the AuAg/ZIF-8 catalyst (35.2%) in the selective oxidation of benzyl alcohol into benzaldehyde. The effect of the solvent, reaction temperature, reaction time, and reaction pressure on benzyl alcohol conversion and benzaldehyde selectivity in benzyl alcohol selective oxidation over Au@Ag/ZIF-8, Ag@Au/ZIF-8, and AuAg/ZIF-8 were also investigated. All of the catalysts showed excellent performance at 130 °C under 8 bar O2 within 1 h when using THF as the solvent in the selective oxidation of benzyl alcohol to benzaldehyde. Moreover, the catalysts can be easily recycled and used repetitively at least four times.
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Dissertations / Theses on the topic "Core shell structured catalyst"

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Haibo, E. "Quantitative analysis of core-shell nanoparticle catalysts by scanning transmission electron microscopy." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:19c3b989-0ffb-487f-8cb3-f6e9dea83e63.

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This thesis concerns the application of aberration corrected scanning transmission electron microscopy (STEM) to the quantitative analysis of industrial Pd-Pt core-shell catalyst nanoparticles. High angle annular dark field imaging (HAADF), an incoherent imaging mode, is used to determine particle size distribution and particle morphology of various particle designs with differing amounts of Pt coverage. The limitations to imaging, discrete tomography and spectral analysis imposed by the sample’s sensitivity to the beam are also explored. Since scattered intensity in HAADF is strongly dependent on both thickness and composition, determining the three dimensional structure of a particle and its bimetallic composition in each atomic column requires further analysis. A quantitative method was developed to interpret single images, obtained from commercially available microscopes, by analysis of the cross sections of HAADF scattering from individual atomic columns. This technique uses thorough detector calibrations and full dynamical simulations in order to allow comparison between experimentally measured cross section to simulated ones and is shown to be robust to many experimental parameters. Potential difficulties in its applications are discussed. The cross section approach is tested on model materials before applying it to the identification of column compositions of core-shell nanoparticles. Energy dispersive X-ray analysis is then used to provide compositional sensitivity. The potential sources of error are discussed and steps towards optimisation of experimental parameters presented. Finally, a combination of HAADF cross section analysis and EDX spectrum imaging is used to investigate the core-shell nanoparticles and the results are correlated to findings regarding structure and catalyst activity from other techniques. The results show that analysis by cross section combined with EDX spectrum mapping shows great promise in elucidating the atom-by-atom composition of individual columns in a core-shell nanoparticle. However, there is a clear need for further investigation to solve the thickness / composition dualism.
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Liu, Chen. "Structural Studies of Pt-Based Electrocatalysts for Polymer Electrolyte Fuel Cells." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263807.

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付記する学位プログラム名: 京都大学大学院思修館
京都大学
新制・課程博士
博士(総合学術)
甲第23346号
総総博第19号
京都大学大学院総合生存学館総合生存学専攻
(主査)教授 寶 馨, 教授 内本 喜晴, 特定教授 橋本 道雄
学位規則第4条第1項該当
Doctor of Philosophy
Kyoto University
DFAM
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直也, 青木, and Naoya Aoki. "固体高分子形燃料電池用高活性・高耐久コアシェル触媒の新規合成法に関する研究." Thesis, https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB13158528/?lang=0, 2021. https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB13158528/?lang=0.

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Cho, Sung-Jin. "Synthesis and characterization of core/shell structured magnetic nanomaterials /." For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2005. http://uclibs.org/PID/11984.

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Ceylan, Abdullah. "Core/shell structured magnetic nanoparticles synthesized by inert gas condensation." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 139 p, 2007. http://proquest.umi.com/pqdweb?did=1397915001&sid=7&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Williams, Benjamin Parker. "Using Core-Shell Nanocatalysts to Unravel the Impact of Surface Structure on Catalytic Activity:." Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:108918.

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Thesis advisor: Udayan Mohanty
The high surface area and atomic-level tunability offered by nanoparticles has defined their promise as heterogeneous catalysts. While initial studies began with nanoparticles of a single metal assuming thermodynamic shapes, modern work has focused on using nanoparticle composition and geometry to optimize nanocatalysts for a wide variety of reactions. Further optimization of these refined nanocatalysts remains difficult, however, as the factors that determine catalytic activity are intertwined and a fundamental understanding of each remains elusive. In this work, precise synthetic methods are used to tune a number of factors, including composition, strain, metal-to-metal charge transfer, atomic order, and surface faceting, and understand their impact on catalysis. The first chapter focuses on current achievements and challenges in the synthesis of intermetallic nanocatalysts, which offer long-range order that allows for total control of surface structure. A particular focus is given to the impact of the synthetic approach on the activity of the resulting nanoparticles. In the second chapter, multilayered Pd-(Ni-Pt)x nanoparticles serve as a controlled arena for the study of metallic mixing and order formation on the nanoscale. The third chapter controls the shell thickness of Au@PdPt core-alloyed shell nanoparticles on a nanometer scale to isolate strain at the nanoparticle surface. In the fourth chapter, the synthetic approaches of chapters two and three are applied to catalysis. In totality, the work presented here represents a brick in the foundation of understanding and exploiting structure-function relationships on the nanoscale, with an eye toward the rational design of tailored nanocatalysts
Thesis (PhD) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
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De, Clercq Astrid. "In-situ study of the growth, structure and reactivity of Pt-Pd nanoalloys." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4077/document.

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Les propriétés catalytiques des nanoparticules métalliques peuvent être améliorées par effet d’alliages. La synthèse en solution par voie colloïdale permet de préparer des nanoalliages homogènes en taille, en forme et en composition chimique, de structure ordonnée, désordonnée ou cœur-coquille. La nucléation et la croissance des nanoalliages de Pt-Pd sont étudiées ici par microscopie électronique en transmission, en condition standard, puis in situ dans une cellule liquide formée par des feuilles d’oxyde de graphène. La cinétique de croissance des nanoalliages de Pt-Pd correspond à l’incorporation directe des monomères en solution, compatible avec un processus limité par la réaction de surface, sans phénomène de coalescence, contrairement à la croissance du Pt pur. La structure théorique à l’équilibre des nanoalliages de Pt-Pd est déterminée par des simulations Monte Carlo. La structure la plus probable correspond à une surface riche en Pd et à une sous couche atomique riche en Pt, stable à des températures élevées. L’effet de l’adsorption de gaz oxydants ou réducteurs sur la forme des nanoparticules, est étudié in situ par microscopie environnementale sous pression de quelques mbar, dans un porte objet environnemental. On observe des changements de formes sous oxygène, dus au développement de facettes d’indices plus élevés. La réactivité des nanocubes de Pd@Pt est étudiée pour l’oxydation du CO en fonction du recouvrement de Pt à la surface. La réactivité maximale pour un faible recouvrement est interprétée par une baisse de l’énergie d’adsorption du CO liée au désaccord paramétrique entre le Pt et le Pd et à la modification de la structure électronique du Pt lié au Pd
The catalytic properties of metal nanoparticles can be improved by the alloying effect. Nanoalloys homogeneous in size, shape and chemical composition can be prepared with the colloidal synthesis method, with an ordered, random or core-shell chemical structure. Nucleation and growth of colloidal Pt-Pd nanoalloys were studied by transmission electron microscopy (TEM), in standard conditions and in situ with the aid of a graphene oxide liquid cell. The growth kinetics of homogeneous Pt-Pd nanoalloys corresponds to the direct incorporation of the monomers in solution. It was compatible with a process limited by the surface reaction, without coalescence (Lifshitz-Slyozov-Wagner mechanism). On the contrary, coalescence occurs during the growth of pure Pt nanoparticles. The theoretical structure of Pt-Pd nanoalloys is determined by Monte Carlo simulations. The most stable structure corresponds to a Pd surface and Pt subsurface layer, which is stable up to high temperatures. The effect of adsorption of oxidizing or reducing gasses on the shape of pure Pd nanocubes and core-shell Pd@Pt nanocubes is studied in situ by TEM with an environmental cell. The observed changes in a few mbar of oxygen are due to the development of higher index facets. The CO oxidation reaction is used to compare the reactivity of homogeneous Pt-Pd nanoalloys and core-shell Pd@Pt nanocubes with increasing coverage of Pt at the surface. A maximal reactivity is attained for a low coverage. The effect is interpreted by a decrease in adsorption energy of CO, due to electronic effects originating from the lattice mismatch between Pt and Pd and the mixed Pt-Pd bonds
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Hu, Pan. "Surfactant Directed Encapsulation of Metal Nanocrystals in Metal-Organic Frameworks." Thesis, Boston College, 2015. http://hdl.handle.net/2345/bc-ir:104132.

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Thesis advisor: Dunwei Wang
Metal nanocrystals with size and shape control have great potential in heterogeneous catalysis. Controllable encapsulation of well-defined metal nanoparticles into the novel porous materials results in new multifunctional nanomaterials. The core-shell nanostructure can enhance the selectivity, durability, or reactivity of the catalysts and even provide additional functionalities. Metal-organic frameworks (MOFs) are a class of novel crystalline nanoporous materials, with well-defined pore structures and distinctive chemical properties. Using MOFs as the encapsulating porous materials has drawn great interest recently due to their tunable structures and properties. However, it could be challenging to grow another porous material layer on metal surface due to the unfavorable interfacial energy. In this work we develop a new concept of colloidal synthesis to synthesize the metal@MOF core-shell nanostructures, in which a layer of self-assembled molecules directed the growth and alignment between two materials. Surfactant cetyltrimethylammonium bromide (CTAB) is designated to facilitate the overgrowth of MOF onto metal surface, and an alignment between the {100} planes of the metal and {110} planes of the MOF can be observed. By utilizing the same concept, a third layer of mesoporous silica could also be coated on the MOF shell with assistance of CTAB. And our method could be a general strategy to fabricate multiple-layer MOF materials
Thesis (MS) — Boston College, 2015
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
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Zhang, Furui. "Mechanism and Interface Study of One-to-one Metal NP/Metal Organic Framework Core-shell Structure." Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107565.

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Thesis advisor: Chia-Kuang (Frank) Tsung
The core-shell hybrid structure is the simplest motif of two-component systems which consists of an inner core coated by an outer shell. Core-shell composite materials are attractive for their biomedical, electronic and catalytic applications in which interface between core and shell is critical for various functionalities. However, it is still challenging to study the exact role that interface plays during the formation of the core-shell structures and in the properties of the resulted materials. By studying the formation mechanism of a well interface controlled one-to-one metal nanoparticle (NP)@zeolite imidazolate framework-8 (ZIF-8) core-shell material, we found that the dissociation of capping agents on the NP surface results in direct contact between NP and ZIF-8, which is essential for the formation of core-shell structure. And the amount of capping agents on the NP surface has a significant effect to the crystallinity and stability of ZIF-8 coating shell. Guided by our understanding to the interface, one-to-one NP@UiO-66 core-shell structure has also been achieved for the first time. We believe that our research will help the development of rational design and synthesis of core-shell structures, particularly in those requiring good interface controls
Thesis (MS) — Boston College, 2017
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
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Otor, Hope O. "Catalyst Development and Control of Catalyst Deactivation for Carbon Dioxide Conversion." University of Toledo / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1596134702392137.

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Book chapters on the topic "Core shell structured catalyst"

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Miyake, Koji, and Norikazu Nishiyama. "Core–Shell Structured Zeolite Catalysts with Enhanced Shape Selectivity." In Core-Shell and Yolk-Shell Nanocatalysts, 181–86. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_11.

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Das, Sonali, and Sibudjing Kawi. "Core-Shell Structured Catalysts for Catalytic Conversion of CO2 to Syngas." In Core-Shell and Yolk-Shell Nanocatalysts, 121–49. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_8.

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Huang, He, Weixiao Ji, and Wei Wang. "Organic Transformations Enabled by Yolk–Shell and Core–Shell Structured Catalysts." In Core-Shell and Yolk-Shell Nanocatalysts, 479–92. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_29.

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Chang, Shuai, Soon Hee Park, Chang Hwan Kim, and Sung June Cho. "Tailoring of Core Shell Like Structure in PdPt Bimetallic Catalyst for Catalytic Application." In Core-Shell and Yolk-Shell Nanocatalysts, 289–302. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_19.

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Okamoto, Masaki. "Core–Shell Structured Zeolite Catalysts with Minimal Defects for Improvement of Shape Selectivity." In Core-Shell and Yolk-Shell Nanocatalysts, 187–98. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_12.

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Wen, Meicheng, Kohsuke Mori, Yasutaka Kuwahara, Guiying Li, Taicheng An, and Hiromi Yamashita. "Synthesis of Plasmonic Catalyst with Core-Shell Structure for Visible Light Enhanced Catalytic Performance." In Core-Shell and Yolk-Shell Nanocatalysts, 233–43. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_15.

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Li, Guodong, and Zhiyong Tang. "Fabrication of Core–Shell Structured Metal Nanoparticles@Metal–Organic Frameworks for Heterogeneous Thermal Catalysis." In Core-Shell and Yolk-Shell Nanocatalysts, 83–103. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_6.

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Zong, Zi Yi, Xi Jiang Yin, Li Fang Lew, and Soo Yee Tan. "SiO2 (core)-TiO2 (shell) Structure as Catalyst Support for Oxidation of CO at Low Temperatures." In Advances in Composite Materials and Structures, 1025–28. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-427-8.1025.

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Suzuki, Ken. "Aerobic Oxidative Esterification of Aldehydes with Alcohols by Gold–Nickel Oxide Nanoparticle Catalysts with a Core–Shell Structure." In Core-Shell and Yolk-Shell Nanocatalysts, 13–24. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_2.

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Chang, Fangfang, Lingyan Jing, Yash Boyjoo, Jian Liu, and Qihua Yang. "Yolk-Shell Structured Functional Nanoreactors for Organic Transformations." In Core-Shell and Yolk-Shell Nanocatalysts, 379–94. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0463-8_23.

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Conference papers on the topic "Core shell structured catalyst"

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Choi, H. J., I. B. Jang, J. Y. Lee, A. Pich, S. Bhattacharya, and H. J. Alder. "Magnetorheology of synthesized core-shell structured nanoparticle." In INTERMAG Asia 2005: Digest of the IEEE International Magnetics Conference. IEEE, 2005. http://dx.doi.org/10.1109/intmag.2005.1464207.

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CHOI, H. J., M. S. CHO, and I. S. LEE. "ELETRORHEOLOGY OF MONODISPERSE CORE/SHELL STRUCTURED PARTICLE SUSPENSIONS." In Proceedings of the Ninth International Conference. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702197_0003.

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Wang, Xuefeng, Yarong Cheng, Li Su, Pengcheng Xu, and Xinxin Li. "Formaldehyde Sensor with Pentagram-Shaped Core-Shell Nanostructure as Catalyst." In 2021 21st International Conference on Solid-State Sensors, Actuators and Microsystems (Transducers). IEEE, 2021. http://dx.doi.org/10.1109/transducers50396.2021.9495612.

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Hyunsuk Kim, Byungjun Park, Kyoungah Cho, Jin-Hyoung Kim, Jun Woo Lee, and Sangsig Kim. "Charge transport of HgTe/CdTe core-shell structured nanoparticles." In Digest of Papers. 2004 International Microprocesses and Nanotechnology Conference, 2004. IEEE, 2004. http://dx.doi.org/10.1109/imnc.2004.245769.

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Uesugi, Akio, Shinya Nakata, Kodai Inoyama, Koji Sugano, and Yoshitada Isono. "Anomalous Piezoresistive Changes of Core-Shell Structured SIC Nanowires." In 2021 IEEE 34th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2021. http://dx.doi.org/10.1109/mems51782.2021.9375210.

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Su, Sena, Mehmet Eroglu, Cevriye Kalkandelen, Nazmi Ekren, Faik Nuzhet Oktar, Mahir Mahirogullari, and Oguzhan Gunduz. "Core-shell structured hyaluronic acid and keratin nanofibers for wound dressing." In 2019 Medical Technologies Congress (TIPTEKNO). IEEE, 2019. http://dx.doi.org/10.1109/tiptekno.2019.8895083.

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Rabbani, Mahboubeh, Rahmatollah Rahimi, and Mahdi Heidari-Golafzani. "Preparation and Photocatalytic Application of Zn-Fe2O4@ZnO Core-Shell Structured Spheres." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b003.

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Dong, Lin, Andrea Pinos, Abhilash Sugunan, Shanghua Li, Sergei Popov, Muhammet Toprak, Ari T. Friberg, and Mamoun Muhammed. "Measurement of Radiative Lifetime in CdSe/CdS Core/shell Structured Quantum Dots." In Asia Communications and Photonics Conference and Exhibition. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/acp.2009.fw6.

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Wang, Fan, Minghui Nan, Sunghoon Cho, Chang-Sei Kim, Jong-Oh Park, and Eunpyo Choi. "Bioinspired Ionic Soft Actuator Based on Core-Shell-Structured Bacterial Cellulose Membrane." In 2018 International Conference on Manipulation, Automation and Robotics at Small Scales (MARSS). IEEE, 2018. http://dx.doi.org/10.1109/marss.2018.8481151.

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Morais, Amanda de, Fernando Sigoli, Flávia Ferreira, and Italo Mazali. "Comparative study of hierarchically structured and bifunctional core-shell rare earth nanoparticles." In Congresso de Iniciação Científica UNICAMP. Universidade Estadual de Campinas, 2019. http://dx.doi.org/10.20396/revpibic2720192250.

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