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author:

Ding, Xueda (Ding, Xueda.) [1] | Huang, Yuxin (Huang, Yuxin.) [2] | Chen, Dongyang (Chen, Dongyang.) [3] | Xie, Zailai (Xie, Zailai.) [4]

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Abstract:

Constructing heterojunction interface as an active catalyst is an effective strategy to boost electrocatalytic activity of oxygen evolution reaction (OER). Herein, we report an interfacial CoP/CeO2 heterostructure catalyst constructed by interface engineering and selective phosphorization procedure. X-ray photoelectron spectroscopy (XPS) suggests that coupling CeO2 nanoparticles on the surface of CoP will generate interfacial interaction at the two-phase interface, resulting in electron transfer between CoP and CeO2 components at the interface. Benefitting from the interfacial interaction, large exposed interface area, and luxuriant mesopores structure, CoP/CeO2 shows fascinating alkaline OER performance. At the current densities of 10 and 50 mA cm−2, the optimal CoP/CeO2 heterojunction exhibits lower overpotential (257 and 298 mV) than either CoP (288 and 354 mV) or RuO2 (305 and 409 mV). This work provides a facile synthetic protocol for constructing heterostructure interfaces to improve OER performance. © 2023 Chinese Society of Particuology and Institute of Process Engineering, Chinese Academy of Sciences

Keyword:

Catalyst activity Cerium oxide Heterojunctions Nanocatalysts Nanoparticles Oxygen Phase interfaces Ruthenium compounds X ray photoelectron spectroscopy

Community:

  • [ 1 ] [Ding, Xueda]College of Materials Science and Engineering, Fuzhou University, Fuzhou; 350116, China
  • [ 2 ] [Huang, Yuxin]College of Chemistry, Fuzhou University, Fuzhou; 350116, China
  • [ 3 ] [Chen, Dongyang]College of Materials Science and Engineering, Fuzhou University, Fuzhou; 350116, China
  • [ 4 ] [Xie, Zailai]College of Chemistry, Fuzhou University, Fuzhou; 350116, China

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Source :

Particuology

ISSN: 1674-2001

Year: 2023

Volume: 81

Page: 38-44

4 . 1

JCR@2023

4 . 1 0 0

JCR@2023

ESI HC Threshold:49

JCR Journal Grade:2

CAS Journal Grade:3

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count: 9

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 3

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