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作者:

Lin Lili (Lin Lili.) | Yu Qiaolin (Yu Qiaolin.) | Peng Mi (Peng Mi.) | Li Aowen (Li Aowen.) | Yao Siyu (Yao Siyu.) | Tian Shuheng (Tian Shuheng.) | Liu Xi (Liu Xi.) | Li Ang (Li Ang.) (学者:李昂) | Jiang Zheng (Jiang Zheng.) | Gao Rui (Gao Rui.) | Han Xiaodong (Han Xiaodong.) (学者:韩晓东) | Li Yong-Wang (Li Yong-Wang.) | Wen Xiao-Dong (Wen Xiao-Dong.) | Zhou Wu (Zhou Wu.) | Ma Ding (Ma Ding.)

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摘要:

Methanol-water reforming is a promising solution for H2 production/transportation in stationary and mobile hydrogen applications. Developing inexpensive catalysts with sufficiently high activity, selectivity, and stability remains challenging. In this paper, nickel-supported over face-centered cubic (fcc) phase α-MoC has been discovered to exhibit extraordinary hydrogen production activity in the aqueous-phase methanol reforming reaction. Under optimized condition, the hydrogen production rate of 2% Ni/α-MoC is about 6 times higher than that of conventional noble metal 2% Pt/Al2O3 catalyst. We demonstrate that Ni is atomically dispersed over α-MoC via carbon bridge bonds, forming a Ni1-C
x
 motif on the carbide surface. Such Ni1-C
x
 motifs can effectively stabilize the isolated Ni1 sites over the α-MoC substrate, rendering maximized active site density and high structural stability. In addition, the synergy between Ni1-C
x
 motif and α-MoC produces an active interfacial structure for water dissociation, methanol activation, and successive reforming processes with compatible activity.

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作者机构:

  • [ 1 ] [Lin Lili]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China
  • [ 2 ] [Yu Qiaolin]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China
  • [ 3 ] [Peng Mi]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China
  • [ 4 ] [Li Aowen]School of Physical Sciences and CAS Key Laboratory of Vacuum Physics, University of Chinese Academy of Sciences, Beijing 100049, China
  • [ 5 ] [Yao Siyu]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China
  • [ 6 ] [Tian Shuheng]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China
  • [ 7 ] [Liu Xi]School of Chemistry and Chemical, In-situ Center for Physical Science, Shanghai Jiao Tong University, Shanghai 200240, China
  • [ 8 ] [Li Ang]Beijing Key Laboratory of Microstructure and Property of Advanced Materials, Beijing University of Technology, Beijing 100024, China
  • [ 9 ] [Jiang Zheng]Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201204, China
  • [ 10 ] [Gao Rui]State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
  • [ 11 ] [Han Xiaodong]Beijing Key Laboratory of Microstructure and Property of Advanced Materials, Beijing University of Technology, Beijing 100024, China
  • [ 12 ] [Li Yong-Wang]State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
  • [ 13 ] [Wen Xiao-Dong]State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
  • [ 14 ] [Zhou Wu]School of Physical Sciences and CAS Key Laboratory of Vacuum Physics, University of Chinese Academy of Sciences, Beijing 100049, China
  • [ 15 ] [Ma Ding]Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing 100871, China

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来源 :

Journal of the American Chemical Society

ISSN: 1520-5126

年份: 2021

期: 1

卷: 143

页码: 309-317

1 5 . 0 0 0

JCR@2022

ESI学科: CHEMISTRY;

ESI高被引阀值:96

JCR分区:1

被引次数:

WoS核心集被引频次: 0

SCOPUS被引频次: 219

ESI高被引论文在榜: 0 展开所有

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