Jiang Yawen, Wang Xinyu, Duan Delong, He Chaohua, Ma Jun, Zhang Wenqing, Liu Hengjie, Long Ran, Li Zibiao, Kong Tingting, Loh Xian Jun, Song Li, Ye Enyi, Xiong Yujie
Hefei National Laboratory for Physical Sciences at the Microscale, Frontiers Science Center for Planetary Exploration and Emerging Technologies, School of Chemistry and Materials Science, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research), 2 Fusionopolis Way, Innovis, #08-03, Singapore, 138634, Singapore.
Adv Sci (Weinh). 2022 May;9(16):e2105292. doi: 10.1002/advs.202105292. Epub 2022 Apr 1.
Structural reconstruction is a process commonly observed for Cu-based catalysts in electrochemical CO reduction. The Cu-based precatalysts with structural complexity often undergo sophisticated structural reconstruction processes, which may offer opportunities for enhancing the electrosynthesis of multicarbon products (C products) but remain largely uncertain due to various new structural features possibly arising during the processes. In this work, the Cu O superparticles with an assembly structure are demonstrated to undergo complicated structure evolution under electrochemical reduction condition, enabling highly selective CO -to-C products conversion in electrocatalysis. As revealed by electron microscopic characterization together with in situ X-ray absorption spectroscopy and Raman spectroscopy, the building blocks inside the superparticle fuse to generate numerous grain boundaries while those in the outer shell detach to form nanogap structures that can efficiently confine OH to induce high local pH. Such a combination of unique structural features with local reaction environment offers two important factors for facilitating C-C coupling. Consequently, the Cu O superparticle-derived catalyst achieves high faradaic efficiencies of 53.2% for C H and 74.2% for C products, surpassing the performance of geometrically simpler Cu O cube-derived catalyst and most reported Cu electrocatalysts under comparable conditions. This work provides insights for rationally designing highly selective CO reduction electrocatalysts by controlling structural reconstruction.
结构重构是电化学CO还原中铜基催化剂常见的过程。具有结构复杂性的铜基预催化剂通常会经历复杂的结构重构过程,这可能为增强多碳产物(C产物)的电合成提供机会,但由于过程中可能出现的各种新结构特征,其情况仍很大程度上不确定。在这项工作中,具有组装结构的CuO超粒子被证明在电化学还原条件下会经历复杂的结构演变,从而在电催化中实现高选择性的CO到C产物转化。通过电子显微镜表征以及原位X射线吸收光谱和拉曼光谱揭示,超粒子内部的构建块融合产生大量晶界,而外壳中的构建块分离形成纳米间隙结构,该结构可有效限制OH以诱导高局部pH值。这种独特的结构特征与局部反应环境的结合为促进C-C偶联提供了两个重要因素。因此,由CuO超粒子衍生的催化剂对C₂H₄的法拉第效率高达53.2%,对C产物的法拉第效率为74.2%,超过了几何结构更简单的CuO立方体衍生催化剂以及在可比条件下大多数已报道的Cu电催化剂的性能。这项工作为通过控制结构重构合理设计高选择性CO还原电催化剂提供了见解。