Wanfeng Yang (4818531)Yong Zhao (84950)Sheng Chen (21971)Wenhao Ren (2561731)Xianjue Chen (1650955)Chen Jia (2794714)Zhen Su (18658)Yuan Wang (14955)Chuan Zhao (1416175)
Electrochemical CO<sub>2</sub> reduction to fuels and chemicals\nis a promising approach for CO<sub>2</sub> utilization. Developing\nhighly active, selective, and cost-effective electrocatalysts is the\nkey to the large-scale application of this technology. Here, we report\nthat defective indium/indium oxide heterostructures selectively catalyze\nCO<sub>2</sub> electroreduction into C<sub>1</sub> products in a broad\npotential range from −0.7 to −1.2 V vs RHE in aqueous\nmedia with the faradaic efficiency approaching 100%. This electrocatalyst\nenables an efficient CO<sub>2</sub>-to-formate conversion with excellent\nselectivity (up to 93%), activity (up to 50.8 mA cm<sup>–2</sup>), and durability (>25 h). The collaboration between metallic\nIn\nand In oxide of the heterostructures attributes to the boosted electrochemical\nCO<sub>2</sub> reduction: Metallic In mainly facilitates formate production,\nwhile In oxide suppresses the competing hydrogen evolution reaction.\nThis study highlights the integration of different functional components/defects\ninto heterostructures as an effective strategy for enhancing CO<sub>2</sub> electrocatalysis.
Wanfeng YangYong ZhaoSheng ChenWenhao RenXianjue ChenChen JiaZhen SuYuan WangChuan Zhao
Jieshu ZhouLiming LiHangxing RenHaibin WangYong LiKangning LiuLiang HuangXinyao YangZhen HaoYuguang ZhangZhichao WangXi WangJian DingYuping JiLi WangHongyan Liang
V. LebedevCh. Y. WangS. HauguthV. M. PolyakovFrank SchwierzV. CimallaThomas KupsFrancisco M. MoralesJ. G. LozanoD. GonzálezMarcel HimmerlichJ.A. SchaeferStefan KrischokO. Ambacher
Guillem Domènech-GilI. GràciaC. CanéA. Romano‐Rodrı́guez
Jiaqi ShaoYi WangDunfeng GaoKe YeQi WangGuoxiong Wang