Zhou Rui, Fan Xing, Ke Xiaoxing, Xu Jie, Zhao Xuan, Jia Lin, Pan Binbin, Han Na, Li Lixing, Liu Xijun, Luo Jun, Lin Haiping, Li Yanguang
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123, China.
Beijing Key Laboratory of Microstructure and Properties of Solids, Faculty of Materials and Manufacturing, Beijing University of Technology, Beijing 100124, China.
Nano Lett. 2021 May 12;21(9):4092-4098. doi: 10.1021/acs.nanolett.1c01113. Epub 2021 Apr 21.
Pd is the only metal that can catalyze electrochemical CO reduction to formate at close-to-zero overpotential. It is unfortunately subjected to severe poisoning by trace CO as the side product and suffers from deteriorating stability and selectivity with increasing overpotential. Here, we demonstrate that alloying Pd with Cu in the form of two-dimensional nanodendrites could enable highly stable and selective formate production. Such unique bimetallic nanostructures are formed as a result of the rapid in-plane growth and suppressed out-of-plane growth by carefully controlling a set of experimental parameters. Thanks to the combined electronic effect and nanostructuring effect, our alloy product catalyzes CO reduction to formate with remarkable stability and selectivity under the working potential as cathodic as -0.4 V. Our results are rationalized by computational simulations, evidencing that Cu atoms weaken the *CO adsorption and stabilize the *OCHO adsorption on neighboring Pd atoms.
钯是唯一一种能够在接近零过电位的情况下催化电化学一氧化碳还原生成甲酸盐的金属。不幸的是,它会因痕量一氧化碳这种副产物而受到严重中毒,并且随着过电位的增加,稳定性和选择性会逐渐变差。在此,我们证明以二维纳米树枝状形式将钯与铜合金化能够实现高度稳定且选择性地生成甲酸盐。通过仔细控制一组实验参数,这种独特的双金属纳米结构是快速的面内生长和抑制的面外生长的结果。得益于电子效应和纳米结构效应的共同作用,我们的合金产物在低至 -0.4 V 的阴极工作电位下催化一氧化碳还原生成甲酸盐时具有显著的稳定性和选择性。我们的结果通过计算模拟得到了合理的解释,证明铜原子减弱了 *CO 的吸附并稳定了相邻钯原子上的 *OCHO 吸附。