Designs of Tandem Catalysts and Cascade Catalytic Systems for CO2 Upgrading

Author:

Zheng Wanzhen1,Yang Xiaoxuan1,Li Zhongjian1,Yang Bin1,Zhang Qinghua1,Lei Lecheng1,Hou Yang12ORCID

Affiliation:

1. Key Laboratory of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou Zhejiang 310027 China

2. Institute of Zhejiang University, Quzhou Quzhou Zhejiang 324000 China

Abstract

AbstractUpgrading CO2 into multi‐carbon (C2+) compounds through the CO2 reduction reaction (CO2RR) offers a practical approach to mitigate atmospheric CO2 while simultaneously producing high value chemicals. The reaction pathways for C2+ production involve multi‐step proton‐coupled electron transfer (PCET) and C−C coupling processes. By increasing the surface coverage of adsorbed protons (*Had) and *CO intermediates, the reaction kinetics of PCET and C−C coupling can be accelerated, thereby promoting C2+ production. However, *Had and *CO are competitively adsorbed intermediates on monocomponent catalysts, making it difficult to break the linear scaling relationship between the adsorption energies of the *Had/*CO intermediate. Recently, tandem catalysts consisting of multicomponents have been developed to improve the surface coverage of *Had or *CO by enhancing water dissociation or CO2‐to‐CO production on auxiliary sites. In this context, we provide a comprehensive overview of the design principles of tandem catalysts based on reaction pathways for C2+ products. Moreover, the development of cascade CO2RR catalytic systems that integrate CO2RR with downstream catalysis has expanded the range of potential CO2 upgrading products. Therefore, we also discuss recent advancements in cascade CO2RR catalytic systems, highlighting the challenges and perspectives in these systems.

Funder

National Natural Science Foundation of China

National Archives and Records Administration

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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