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author:

Fang, Zhongpu (Fang, Zhongpu.) [1] | Liang, Yingsi (Liang, Yingsi.) [2] | Li, Yanli (Li, Yanli.) [3] | Ni, Bilian (Ni, Bilian.) [4] | Zhu, Jia (Zhu, Jia.) [5] | Li, Yi (Li, Yi.) [6] (Scholars:李奕) | Huang, Shuping (Huang, Shuping.) [7] (Scholars:黄淑萍) | Lin, Wei (Lin, Wei.) [8] (Scholars:林伟) | Zhang, Yongfan (Zhang, Yongfan.) [9] (Scholars:章永凡)

Indexed by:

EI Scopus SCIE

Abstract:

The catalytic mechanisms of nitrogen reduction reaction (NRR) on the pristine and Co/alpha-MoC(001) surfaces were explored by density functional theory calculations. The results show that the preferred pathway is that a direct N equivalent to N cleavage occurs first, followed by continuous hydrogenations. The production of second NH3 molecule is identified as the rate-limiting step on both systems with kinetic barriers of 1.5 and 2.0 eV, respectively, indicating that N-2-to-NH3 transformation on bimetallic surface is more likely to occur. The two components of the bimetallic center play different roles during NRR process, in which Co atom does not directly participate in the binding of intermediates, but primarily serves as a reservoir of H atoms. This special synergy makes Co/alpha-MoC(001) have superior activity for ammonia synthesis. The introduction of Co not only facilitates N-2 dissociation, but also accelerates the migration of H atom due to the antibonding characteristic of Co-H bond. This study offers a facile strategy for the rational design and development of efficient catalysts for ammonia synthesis and other reactions involving the hydrogenation processes.

Keyword:

Density functional theory Molybdenum carbide Nitrogen reduction reaction Reaction mechanism Single-atom catalyst

Community:

  • [ 1 ] [Fang, Zhongpu]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 2 ] [Liang, Yingsi]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 3 ] [Li, Yanli]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 4 ] [Li, Yi]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 5 ] [Huang, Shuping]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 6 ] [Lin, Wei]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 7 ] [Zhang, Yongfan]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China
  • [ 8 ] [Ni, Bilian]Fujian Med Univ, Coll Pharm, Dept Basic Chem, Fuzhou 350122, Fujian, Peoples R China
  • [ 9 ] [Zhu, Jia]Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
  • [ 10 ] [Li, Yi]Fujian Prov Key Lab Theoret & Computat Chem, Xiamen 361005, Fujian, Peoples R China
  • [ 11 ] [Lin, Wei]Fujian Prov Key Lab Theoret & Computat Chem, Xiamen 361005, Fujian, Peoples R China
  • [ 12 ] [Zhang, Yongfan]Fujian Prov Key Lab Theoret & Computat Chem, Xiamen 361005, Fujian, Peoples R China

Reprint 's Address:

  • [Zhang, Yongfan]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Fujian, Peoples R China;;[Ni, Bilian]Fujian Med Univ, Coll Pharm, Dept Basic Chem, Fuzhou 350122, Fujian, Peoples R China;;[Zhang, Yongfan]Fujian Prov Key Lab Theoret & Computat Chem, Xiamen 361005, Fujian, Peoples R China;;

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Source :

CHEMISTRY-A EUROPEAN JOURNAL

ISSN: 0947-6539

Year: 2023

Issue: 9

Volume: 30

3 . 9

JCR@2023

3 . 9 0 0

JCR@2023

JCR Journal Grade:2

CAS Journal Grade:3

Cited Count:

WoS CC Cited Count: 1

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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