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Interfacial Metal Oxides Stabilize Cu Oxidation States for Electrocatalytical CO 2 Reduction
Author(s) -
Zhao Yajie,
Wang Haoyuan,
Liu Chunxiao,
Ji Yuan,
Li Xu,
Jiang Qiu,
Zheng Tingting,
Xia Chuan
Publication year - 2025
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.202402510
Subject(s) - metal , copper , inorganic chemistry , chemistry , oxide , redox , oxidation state , materials science , reduction (mathematics) , chemical engineering , organic chemistry , geometry , mathematics , engineering
Abstract Modulating the oxidation state of copper (Cu) is crucial for enhancing the electrocatalytic CO 2 reduction reaction (CO 2 RR), particularly for facilitating deep reductions to produce methane (CH 4 ) or multi‐carbon (C 2+ ) products. However, Cu δ+ sites are thermodynamically unstable, fluctuating their oxidation states under reaction conditions, which complicates their functionality. Incorporating interfacial metal oxides has emerged as an effective strategy for stabilizing these oxidation states. This review provides an in‐depth examination of the reaction mechanisms occurring at oxide‐modified Cu δ+ sites, offering a comprehensive understanding of their behavior. We explore how Cu/metal oxide interfaces stabilize Cu oxidation states, showing that oxides‐modified Cu catalysts often enhance selectivity for C 2+ or CH 4 products by stabilizing Cu + or Cu 2+ sites. In addition, we discuss innovative strategies for the rational design of efficient Cu catalytic sites tailored for specific deep CO 2 RR products. The review concludes with an outlook on current challenges and future directions, offering new insights into the rational design of selective and efficient CO 2 RR catalysts.
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