Hu Congling, Li Lulu, Deng Wanyu, Zhang Gong, Zhu Wenjin, Yuan Xintong, Zhang Lei, Zhao Zhi-Jian, Gong Jinlong
Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Collaborative Innovation Center of Chemical Science and Engineering, Tianjin, 300072, P.R. China.
ChemSusChem. 2020 Dec 7;13(23):6353-6359. doi: 10.1002/cssc.202000557. Epub 2020 Apr 7.
The development of electrochemical CO conversion allows green carbon utilization. Formate and syngas are two typical products of electrochemical CO reduction, and the coproduction of these two products will maximize the energy efficiency of CO conversion. However, few works have successfully achieved the cogeneration of formate and syngas. This paper describes a novel strategy to maximize the efficiency of CO conversion through coproduction of formate and syngas on ultrasmall SnO nanodots (NDs) homogeneously anchored on carbon nanotubes (CNT#SnO NDs) electrodes. The CNT#SnO NDs not only decreased the adsorption energy of *OCHO but also reduced the adsorption energy difference of *COOH and *H. High energy efficiency toward formate and adjustable H /CO ratio were obtained over a broad potential window with long-term stability. In addition, CNT#SnO NDs and Ir foil were coupled together to construct an electrolyzer for electrochemical CO reduction reaction and oxygen evolution reaction (CO ERR-OER), which also produced formate and syngas with 24 h stability. A promising approach is presented for the electrochemical CO conversion in fuel production.
电化学CO转化的发展实现了绿色碳利用。甲酸盐和合成气是电化学CO还原的两种典型产物,这两种产物的联产将使CO转化的能量效率最大化。然而,很少有研究成功实现甲酸盐和合成气的联产。本文描述了一种通过在均匀锚定在碳纳米管(CNT#SnO纳米点)电极上的超小SnO纳米点上联产甲酸盐和合成气来最大化CO转化效率的新策略。CNT#SnO纳米点不仅降低了OCHO的吸附能,还减小了COOH和*H的吸附能差。在宽电位窗口内获得了对甲酸盐的高能效和可调节的H/CO比,并具有长期稳定性。此外,将CNT#SnO纳米点和Ir箔耦合在一起构建了一个用于电化学CO还原反应和析氧反应(CO ERR-OER)的电解槽,该电解槽也能稳定24小时联产甲酸盐和合成气。为燃料生产中的电化学CO转化提供了一种有前景的方法。