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author:

Chang, Bin (Chang, Bin.) [1] | Pang, Hong (Pang, Hong.) [2] | Raziq, Fazal (Raziq, Fazal.) [3] | Wang, Sibo (Wang, Sibo.) [4] (Scholars:汪思波) | Huang, Kuo-Wei (Huang, Kuo-Wei.) [5] | Ye, Jinhua (Ye, Jinhua.) [6] | Zhang, Huabin (Zhang, Huabin.) [7]

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EI Scopus SCIE

Abstract:

Electrocatalytic CO2 reduction has been developed as a promising and attractive strategy to achieve carbon neutrality for sustainable chemical production. Among various reduction products, multi-carbon (C2+) compounds with higher energy density are desirable value-added products. Herein, we review and discuss the recent progress and challenges in preparing C2+ products. We start with the elaboration of the most recent advancement of carbon-carbon coupling results and the newly proposed mechanisms, which are much more complicated than that of single-carbon products. The complex scenarios involved in the initial CO2 activation process, the catalyst micro/nanostructure design, and mass transfer conditions optimization have been thoroughly discussed. In addition, we also propose the synergistic realization of high C2+ product selectivity through the rational design of the catalyst and elaborate on the influence of electrolytes (anion/cation/pH/ionic liquid) using theoretical calculation analysis and machine learning prediction. Several in situ/operando techniques have been elaborated for tracking the structural evolution and recording the reaction intermediates during electrocatalysis. Additional insights into the triphasic interfacial reaction systems with improved C2+ selectivity are also provided. By presenting these advances and future challenges with potential solutions related to the integral development of electrochemical reduction of carbon dioxide to C2+ products, we hope to shed some light on the forthcoming research on electrochemical carbon dioxide recycling.

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Community:

  • [ 1 ] [Chang, Bin]King Abdullah Univ Sci & Technol KAUST, Chem Program, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
  • [ 2 ] [Raziq, Fazal]King Abdullah Univ Sci & Technol KAUST, Chem Program, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
  • [ 3 ] [Huang, Kuo-Wei]King Abdullah Univ Sci & Technol KAUST, Chem Program, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
  • [ 4 ] [Zhang, Huabin]King Abdullah Univ Sci & Technol KAUST, Chem Program, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
  • [ 5 ] [Chang, Bin]King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal, Saudi Arabia
  • [ 6 ] [Raziq, Fazal]King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal, Saudi Arabia
  • [ 7 ] [Huang, Kuo-Wei]King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal, Saudi Arabia
  • [ 8 ] [Zhang, Huabin]King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal, Saudi Arabia
  • [ 9 ] [Pang, Hong]Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
  • [ 10 ] [Ye, Jinhua]Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
  • [ 11 ] [Wang, Sibo]Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China

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Source :

ENERGY & ENVIRONMENTAL SCIENCE

ISSN: 1754-5692

Year: 2023

Issue: 11

Volume: 16

Page: 4714-4758

3 2 . 4

JCR@2023

3 2 . 4 0 0

JCR@2023

ESI Discipline: ENVIRONMENT/ECOLOGY;

ESI HC Threshold:33

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count: 119

SCOPUS Cited Count: 126

ESI Highly Cited Papers on the List: 6 Unfold All

  • 2025-1
  • 2024-11
  • 2024-9
  • 2024-7
  • 2024-5
  • 2024-3

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 2

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