Xia ZhangJing FuYuyu LiuXiao‐Dong ZhouJinli Qiao
Metal nanoparticles usually exhibit unique catalytic performance, while unfortunately, so far, the Bi nanoparticles (NPs) (<5 nm) have not been employed for the electrochemical reduction of carbon dioxide (ECR-CO2). Here, we report a facile and mild strategy to fabricate Bi nanocrystals in situ decorated on functionalized multiwalled carbon nanotubes (Bi NP@MWCNTs) as a high-performance catalyst for ECR-CO2. The transmission electron microscopy (TEM) images revealed that the Bi NPs with an average particle size of 4.4 nm were uniformly supported on the MWCNTs. The resulting Bi NP@MWCNTs exhibit much higher electrocatalytic activity, Faradaic efficiency (FE), and current density than the Biblank catalyst toward CO2 reduction to formate. At −1.5 V versus SCE (saturated calomel reference electrode), the maximum FE of 95.2% for formate was achieved on a Bi NP@MWCNT catalyst with a current density of 10.7 mA cm−2. MWCNTs play an important role in the markedly enhanced activity for CO2 reduction to formate on Bi NP@MWCNT catalysts. Besides, the formation of the *OCOH intermediate is considered as the rate-limiting step for CO2 conversion to formate on Bi NP@MWCNT catalysts. The results indicate that the as-prepared Bi NP@MWCNT catalysts exhibit promising potential in the electrochemical reduction of CO2 to fuels.
Xia Zhang (41398)Jing Fu (177892)Yuyu Liu (173195)Xiao-Dong Zhou (1440082)Jinli Qiao (5153804)
Peilin DengHongming WangRuijuan QiJiexin ZhuShenghua ChenFan YangLiang ZhouKai QiHongfang LiuBao Yu Xia
Fangqi YangPengfei LiHaoming YuHan XuTonglin YangQuan ZhangJiong LuJie Zhang
Peilin Deng (8150883)Hongming Wang (11756)Ruijuan Qi (3662584)Jiexin Zhu (4249453)Shenghua Chen (8150886)Fan Yang (1413)Liang Zhou (85586)Kai Qi (1731952)Hongfang Liu (39593)Bao Yu Xia (1942657)
Sungjoo KimWan Jae DongSeungo GimWoonbae SohnJae-Yong ParkChul Jong YooHo Won JangJong‐Lam Lee