Shi Jia-Yi, Wang Zhen-Long, Wang Ke-An, Zhu Hai-Bin
School of Chemistry and Chemical Engineering Southeast University Nanjing 211189 China.
School of Chemistry and Chemical Engineering Southeast University Nanjing 211189 China.
J Colloid Interface Sci. 2024 Apr;659:248-256. doi: 10.1016/j.jcis.2023.12.177. Epub 2023 Dec 30.
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/TiO catalyst for both anodic methanol oxidation reaction (MOR) and cathodic carbon dioxide reduction (COR). The in-built abundant CuS/TiO heterointerfaces are found to boost the COR and MOR to produce formate. Based on the unique bifunctionality of CuS/TiO, a paired electrosynthesis of formate was performed with a total Faradaic efficiency (FE) of about 170 %, in which the cathodic COR achieved a formate FE of about 70 %, and the anodic MOR exhibited an almost 100 % formate FE.
将二氧化碳电化学还原为携带能量的化合物或高附加值化学品对于减轻温室效应具有重要意义。然而,为了提高技术经济性,仍然必须替代价值较低的阳极析氧反应(OER)。在此,我们首次报道了一种用于阳极甲醇氧化反应(MOR)和阴极二氧化碳还原反应(COR)的双功能CuS/TiO催化剂。发现大量内置的CuS/TiO异质界面可促进COR和MOR生成甲酸盐。基于CuS/TiO独特的双功能性,进行了甲酸盐的成对电合成,总法拉第效率(FE)约为170%,其中阴极COR的甲酸盐FE约为70%,阳极MOR的甲酸盐FE几乎为100%。