Xu Xiaoqian, Yang Song, Wang Yixiang, Chen Ying, Devi Assa Aravindh Sasikala, Hu Feng
Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies, College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China.
Research Unit of Sustainable Chemistry, Faculty of Technology, University of Oulu, 90014 Oulu, Finland.
Molecules. 2025 Aug 24;30(17):3475. doi: 10.3390/molecules30173475.
Silver is a promising electrocatalyst for electrochemical CO reduction reaction owing to its high selectivity and efficiency for CO production. However, it still faces a fundamental trade-off between reaction activity and stability. Here, we developed a three-dimensional coral-like porous silver (CP-Ag) catalyst through seed-assisted nanoparticle attachment synthesis, which creates a unique architecture featuring interconnected pores and stable grain boundaries (GBs) between constituent Ag nanoparticles (Ag NPs). Compared to normal Ag NPs, CP-Ag demonstrates superior catalytic performance, maintaining >90% Faradaic efficiency (FE) for CO across a wide potential range (-0.6 to -1.0 V vs. RHE) while achieving 2-times higher current density. Importantly, CP-Ag demonstrated an impressive long-term stability by sustaining nearly 90% FE for CO approximately 40 h at a current density of -50 mA cm in a flow cell. The enhanced catalytic performance arises from three factors: (1) the three-dimensional coral-like morphology increases accessible active sites and promotes charge transfer efficiency; (2) stable GBs between interconnected nanoparticles increase reaction activity; (3) more moderate binding on Ag (100) preferentially promotes *CO intermediate formation. Our findings highlight the importance of simultaneously engineering both morphological and crystallographic features to optimize silver catalysts for CO conversion.
由于银对一氧化碳生成具有高选择性和效率,它是一种很有前景的用于电化学一氧化碳还原反应的电催化剂。然而,它在反应活性和稳定性之间仍面临一个基本的权衡。在此,我们通过种子辅助纳米颗粒附着合成法开发了一种三维珊瑚状多孔银(CP-Ag)催化剂,其构建了一种独特的结构,具有相互连接的孔隙以及组成银纳米颗粒(Ag NPs)之间稳定的晶界(GBs)。与普通的Ag NPs相比,CP-Ag表现出卓越的催化性能,在很宽的电位范围(相对于可逆氢电极,-0.6至-1.0 V)内对一氧化碳保持>90%的法拉第效率(FE),同时实现了2倍更高的电流密度。重要的是,在流动池中,CP-Ag在-50 mA cm的电流密度下,对一氧化碳保持近90%的FE约40小时,展现出令人印象深刻的长期稳定性。催化性能的提升源于三个因素:(1)三维珊瑚状形态增加了可及的活性位点并促进电荷转移效率;(2)相互连接的纳米颗粒之间稳定的GBs增加了反应活性;(3)在Ag(100)上更适中的吸附优先促进*CO中间体的形成。我们的研究结果突出了同时设计形态和晶体学特征以优化用于一氧化碳转化的银催化剂的重要性。