Qin Yuntong, Zhan Guangming, Tang Cun, Yang Di, Wang Xibo, Yang Jianhua, Mao Chengliang, Hao Zhentian, Wang Shuangyu, Qin Yixin, Li Hongmei, Chen Ke, Liu Min, Li Jie
School of Physics and Electronics, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China.
School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Nano Lett. 2023 Oct 25;23(20):9227-9234. doi: 10.1021/acs.nanolett.3c01905. Epub 2023 Oct 4.
Crafting vacancies offers an efficient route to upgrade the selectivity and productivity of nanomaterials for CO electroreduction. However, defective nanoelectrocatalysts bear catalytically active vacancies mostly on their surface, with the rest of the interior atoms adiaphorous for CO-to-product conversion. Herein, taking nanosilver as a prototype, we arouse the catalytic ability of internal atoms by creating homogeneous vacancies realized via electrochemical reconstruction of silver halides. The homogeneous vacancies-rich nanosilver, compared to the surface vacancies-dominated counterpart, features a more positive d-band center to trigger an intensified hybridization of the Ag_d orbital with the C_P orbital of the *COOH intermediate, leading to an accelerated CO-to-CO transformation. These structural and electronic merits allow a large-area (9 cm) electrode to generate nearly pure CO with a CO/H Faradaic efficiency ratio of 6932 at an applied current of 7.5 A. These findings highlight the potential of designing new-type defects in realizing the industrialization of electrocatalytic CO reduction.
制备空位为提升用于CO电还原的纳米材料的选择性和生产率提供了一条有效途径。然而,有缺陷的纳米电催化剂的催化活性空位大多位于其表面,其余内部原子对于CO向产物的转化是惰性的。在此,以纳米银为原型,我们通过对卤化银进行电化学重构来产生均匀空位,从而激发内部原子的催化能力。与以表面空位为主的对应物相比,富含均匀空位的纳米银具有更正的d带中心,从而引发Ag_d轨道与*COOH中间体的C_P轨道的增强杂化,导致CO到CO的转化加速。这些结构和电子优势使得大面积(9平方厘米)电极在7.5 A的施加电流下能够产生几乎纯的CO,CO/H法拉第效率比为6932。这些发现突出了设计新型缺陷在实现电催化CO还原工业化方面的潜力。