4.8 Article

Effect of pretreatment atmosphere on CO oxidation over α-Mn2O3 supported gold catalysts

期刊

JOURNAL OF CATALYSIS
卷 264, 期 2, 页码 145-153

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2009.04.006

关键词

Supported gold catalyst; alpha-Mn2O3; CO oxidation; Pretreatment atmosphere; Deactivation

资金

  1. National Natural Science Foundation of China [20633030, 20721063, 20873026]
  2. National Basic Research Program of China [2003CB615807]
  3. National High Technology Research and Development Program of China [2006AA03Z336]
  4. Science and Technology Commission of Shanghai Municipality [08DZ2270500, 07QH14003]
  5. Committee of the Shanghai Education [06SG03]

向作者/读者索取更多资源

The microstructural properties of Au/alpha-Mn2O3 catalysts moderately pretreated under different atmospheres, i.e., O-2, He and H-2, in relation to their activities and stabilities on CO oxidation were investigated. The highest initial activity was obtained for the He-pretreated catalyst, which, however, suffered the most severe deactivation with time on stream. Pretreatment with O-2 resulted in the best stability and had the highest steady-state activity among the three catalysts. TEM results revealed that the pretreatment has a negligible effect on the gold particle size. While the formation of moderate surface oxygen vacancies before reaction was suggested to be responsible for the highest initial activity of He-Au/alpha-Mn2O3, overreduction of the oxide support could explain the inferior activity of the H-2-pretreated catalyst. Based on the XPS and in situ DRIFTS studies, the superior performance of the O-2-pretreated O-2-Au/alpha-Mn2O3 catalyst can be attributed to the creation of a specific oxygen-enriched interface leading to an enhanced metal-support synergy. (C) 2009 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Chemistry, Physical

Exploiting basic principles to control the selectivity of the vapor phase catalytic oxidative cross-coupling of primary alcohols over nanoporous gold catalysts

Lu-Cun Wang, Kara J. Stowers, Branko Zugic, Michelle L. Personick, Monika M. Biener, Juergen Biener, Cynthia M. Friend, Robert J. Madix

JOURNAL OF CATALYSIS (2015)

Article Chemistry, Physical

Methyl ester synthesis catalyzed by nanoporous gold: from 10-9 Torr to 1 atm

Lu-Cun Wang, Kara J. Stowers, Branko Zugic, Monika M. Biener, Juergen Biener, Cynthia M. Friend, Robert J. Madix

CATALYSIS SCIENCE & TECHNOLOGY (2015)

Article Chemistry, Physical

Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts

Lu-Cun Wang, C. M. Friend, Rebecca Fushimi, Robert J. Madix

FARADAY DISCUSSIONS (2016)

Article Chemistry, Physical

Active sites for methanol partial oxidation on nanoporous gold catalysts

Lu-Cun Wang, Michelle L. Personick, Stavros Karakalos, Rebecca Fushimi, Cynthia M. Friend, Robert J. Madix

JOURNAL OF CATALYSIS (2016)

Article Chemistry, Physical

Dynamic restructuring drives catalytic activity on nanoporous gold-silver alloy catalysts

Branko Zugic, Lucun Wang, Christian Heine, Dmitri N. Zakharov, Barbara A. J. Lechner, Eric A. Stach, Juergen Biener, Miquel Salmeron, Robert J. Madix, Cynthia M. Friend

NATURE MATERIALS (2017)

Article Chemistry, Physical

Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts

Lu-Cun Wang, C. M. Friend, Rebecca Fushimi, Robert J. Madix

FARADAY DISCUSSIONS (2016)

Article Chemistry, Applied

Oxygen Adsorption and Low-Temperature CO Oxidation on a Nanoporous Au Catalyst: Reaction Mechanism and Foreign Metal Effects

L. C. Wang, Y. Zhong, D. Widmann, J. Weissmueller, R. J. Behm

TOPICS IN CATALYSIS (2018)

Article Nanoscience & Nanotechnology

Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

Lu-Cun Wang, Yi Zhong, Haijun Jin, Daniel Widmann, Joerg Weissmueller, R. Juergen Behm

BEILSTEIN JOURNAL OF NANOTECHNOLOGY (2013)

Article Chemistry, Physical

Non-oxidative dehydrogenation of ethane to ethylene over ZSM-5 zeolite supported iron catalysts

Lu-Cun Wang, Yunya Zhang, Jiayi Xu, Weijian Diao, Stavros Karakalos, Bin Liu, Xueyan Song, Wei Wu, Ting He, Dong Ding

APPLIED CATALYSIS B-ENVIRONMENTAL (2019)

Article Chemistry, Applied

Discovery of single-atom alloy catalysts for CO2-to-methanol reaction by density functional theory calculations

Meng Li, Bin Hua, Lu-Cun Wang, Zheng Zhou, Kara J. Stowers, Dong Ding

Summary: The transformation of CO2 into valuable products is an important field of research due to its impact on global warming. Single-atom alloy (SAA) catalysts have shown promising results in CO2 hydrogenation reactions. In this study, the authors used density functional theory (DFT) computations to screen Ru and 6 RuX (X = Fe, Co, Ni, Cu, Ir and Pt) SAAs as potential catalysts. The formation of specific intermediates was found to play a critical role in determining the catalysts' activities, and the doping of Co and Pt single atoms into Ru surface was found to enhance the production of methanol.

CATALYSIS TODAY (2022)

Article Chemistry, Physical

Switching of metal-oxygen hybridization for selective CO2 electrohydrogenation under mild temperature and pressure

Meng Li, Bin Hua, Lu-Cun Wang, Joshua D. Sugar, Wei Wu, Yong Ding, Ju Li, Dong Ding

Summary: Tuning the Ir-O hybridization can alter the catalyst surface chemical environment, enabling the selective production of either CO or CH4 during electrocatalysis. This advanced electrolyser not only enables CO2 electrohydrogenation but also can be extended to the upgrade of different carbon resources, significantly enhancing the techno-economic feasibility of the process.

NATURE CATALYSIS (2021)

Article Chemistry, Applied

Precise non-steady-state characterization of solid active materials with no preliminary mechanistic assumptions

Denis Constales, Gregory S. Yablonsky, Lucun Wang, Weijian Diao, Vladimir V. Galvita, Rebecca Fushimi

CATALYSIS TODAY (2017)

Article Nanoscience & Nanotechnology

Active Site and Electronic Structure Elucidation of Pt Nanoparticles Supported on Phase-Pure Molybdenum Carbide Nanotubes

Shuai Tan, Lucun Wang, Shibely Saha, Rebecca R. Fushimi, Dongmei Li

ACS APPLIED MATERIALS & INTERFACES (2017)

Article Chemistry, Physical

Robust PtRu catalyst regulated via cyclic electrodeposition for electrochemical production of cyclohexanol

Yifan Sun, Ye Lv, Wei Li, Jinli Zhang, Yan Fu

Summary: In this study, PtRu electrocatalysts were fabricated on carbon paper via cyclic electrodeposition for the electrocatalytic hydrogenation (ECH) of phenol. The Pt3Ru3 catalyst exhibited excellent activity and stability for the conversion of phenol to cyclohexanol at ambient temperature and various current densities. The in situ Raman spectroscopy and kinetic study revealed the hydrogenation mechanism of phenol over Pt3Ru3 in acidic electrolyte, providing an effective electrochemical strategy for the facile construction of durable electrode materials and efficient phenol hydrogenation.

JOURNAL OF CATALYSIS (2024)

Article Chemistry, Physical

Escalating the synergism on CdZnS via Ag2S/Cu2S co-catalysts: Boosts hydrogen evolution from water splitting under sunlight

Amir Shahzad, Khezina Rafiq, Muhammad Zeeshan Abid, Naseem Ahmad Khan, Syed Shoaib Ahmad Shah, Raed H. Althomali, Abdul Rauf, Ejaz Hussain

Summary: Photocatalytic hydrogen production through water splitting is an effective method for meeting future energy demands. In this study, researchers synthesized a 1 % Ag2S/Cu2S co-doped CdZnS catalyst and found that it can produce hydrogen at a higher rate. The co-doping of Ag2S and Cu2S in the CdZnS catalyst showed a synergistic effect, with Ag2S promoting oxidation reactions and Cu2S promoting reduction reactions.

JOURNAL OF CATALYSIS (2024)