Synergistic effects of CuS/TiO2 heterointerfaces: Enhanced cathodic CO2 reduction and anodic CH3OH oxidation for paired electrosynthesis of formate

被引:3
|
作者
Shi, Jia-Yi [1 ]
Wang, Zhen-Long [1 ]
Wang, Ke-An [1 ]
Zhu, Hai-Bin [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Peoples R China
基金
中国国家自然科学基金;
关键词
CO; 2; electroreduction; Anodic methanol oxidation; CuS/TiO; Heterointerface; Formate; Paired electrosynthesis; FORMATION MECHANISM; CARBON-DIOXIDE; CUS; ELECTROREDUCTION;
D O I
10.1016/j.jcis.2023.12.177
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical reduction of carbon dioxide into energy-carrying compounds or value-added chemicals is of great significance for diminishing the greenhouse effect. However, it is still imperative to replace the less-value anodic oxygen evolution reaction (OER) to improve the technical economy. Herein, we firstly reported a bifunctional CuS/TiO2 catalyst for both anodic methanol oxidation reaction (MOR) and cathodic carbon dioxide reduction (CO2R). The in-built abundant CuS/TiO2 heterointerfaces are found to boost the CO2R and MOR to produce formate. Based on the unique bifunctionality of CuS/TiO2, a paired electrosynthesis of formate was performed with a total Faradaic efficiency (FE) of about 170 %, in which the cathodic CO2R achieved a formate FE of about 70 %, and the anodic MOR exhibited an almost 100 % formate FE.
引用
收藏
页码:248 / 256
页数:9
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