催化作用
乙炔
X射线光电子能谱
钴
化学
密度泛函理论
酞菁
乙烯
选择性
串联
氧化物
无机化学
光化学
物理化学
材料科学
化学工程
计算化学
有机化学
复合材料
工程类
作者
Jilin Liu,Kai Yu,Zhiyuan Qiao,Qianlong Zhu,Hong Zhang,Jie Jiang
出处
期刊:Chemsuschem
[Wiley]
日期:2023-07-25
卷期号:16 (19): e202300601-e202300601
被引量:5
标识
DOI:10.1002/cssc.202300601
摘要
Abstract Suppressing side reactions and simultaneously enriching key intermediates during CO 2 reduction reaction (CO 2 RR) has been a challenge. Here, we propose a tandem catalyst (Cu 2 O NCs‐C‐Copc) consisting of acetylene black, cobalt phthalocyanine (Copc) and cuprous oxide nanocubes (Cu 2 O NCs) for efficient CO 2 ‐to‐ethylene conversion. Density‐functional theory (DFT) calculation combined with experimental verification demonstrated that Copc can provide abundant CO to nearby copper sites while acetylene black successfully reduces the formation energies of key intermediates, leading to enhanced C 2 H 4 selectivity. X‐ray photoelectron spectroscopy (XPS) and potentiostatic tests indicated that the catalytic stability of Cu 2 O NCs‐C‐Copc was significantly enhanced compared with Cu 2 O NCs. Finally, the industrial application prospect of the catalyst was evaluated using gas diffusion electrolyzers. The of Cu 2 O NCs‐C‐Copc can reach to 58.4 % at −1.1 V vs. RHE in 0.1 M KHCO 3 and 70.3 % at −0.76 V vs. RHE in 1.0 M KOH. This study sheds new light on the design and development of highly efficient CO 2 RR tandem catalytic systems.
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