Garg Sahil, Li Mengran, Hussain Tanveer, Idros Mohamed Nazmi, Wu Yuming, Zhao Xiu Song, Wang Geoff G X, Rufford Thomas E
School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
Department of Physics, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.
ACS Appl Mater Interfaces. 2022 Aug 10;14(31):35504-35512. doi: 10.1021/acsami.2c05918. Epub 2022 Jul 31.
We report a new strategy to improve the reactivity and durability of a membrane electrode assembly (MEA)-type electrolyzer for CO electrolysis to CO by modifying the silver catalyst layer with urea. Our experimental and theoretical results show that mixing urea with the silver catalyst can promote electrochemical CO reduction (COR), relieve limitations of alkali cation transport from the anolyte, and mitigate salt precipitation in the gas diffusion electrode in long-term stability tests. In a 10 mM KHCO anolyte, the urea-modified Ag catalyst achieved CO selectivity 1.3 times better with energy efficiency 2.8-fold better than an untreated Ag catalyst, and operated stably at 100 mA cm with a faradaic efficiency for CO above 85% for 200 h. Our work provides an alternative approach to fabricating catalyst interfaces in MEAs by modifying the catalyst structure and the local reaction environment for critical electrochemical applications such as CO electrolysis and fuel cells.
我们报道了一种新策略,即通过用尿素修饰银催化剂层来提高用于将CO电解为CO的膜电极组件(MEA)型电解槽的反应活性和耐久性。我们的实验和理论结果表明,将尿素与银催化剂混合可以促进电化学CO还原(COR),缓解阳极电解液中碱金属阳离子传输的限制,并在长期稳定性测试中减轻气体扩散电极中的盐沉淀。在10 mM KHCO阳极电解液中,尿素修饰的Ag催化剂的CO选择性比未处理的Ag催化剂提高了1.3倍,能量效率提高了2.8倍,并在100 mA cm下稳定运行200小时,CO的法拉第效率高于85%。我们的工作为通过修饰催化剂结构和局部反应环境来制造MEA中的催化剂界面提供了一种替代方法,用于诸如CO电解和燃料电池等关键电化学应用。