Yang Chao, Shen Hanchen, Guan Anxiang, Liu Junlang, Li Tengfei, Ji Yali, Al-Enizi Abdullah M, Zhang Lijuan, Qian Linping, Zheng Gengfeng
Laboratory of Advanced Materials, Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200438, China.
Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
J Colloid Interface Sci. 2020 Jun 15;570:375-381. doi: 10.1016/j.jcis.2020.03.017. Epub 2020 Mar 6.
Electrochemical CO reduction with rationally designed copper-based electrocatalysts is a promising approach to reduce CO emission and produce value-added products. Grain boundaries and micron-strains inside catalysts have been proposed as active catalytic sites, while the controlled formation of these sites has remained highly challenging. In this work, we developed a strategy of creating high-density grain boundaries and micron-strains inside CuO electrocatalysts by fast cooling with liquid nitrogen. Compared to samples with slower cooling rates, the fast cooled CuO showed clear difference in their crystal domain sizes, micro-strain densities, and the chemisorption capacities of CO and CO. This micro-strain-rich CuO electrocatalyst exhibited a high total current density over 300 mA·cm, and an outstanding Faradaic efficiency for C products (with a majority to ethanol) at -1.0 V vs. reversible hydrogen electrode. Our work suggests a facile approach of tuning grain boundaries and micro-strains inside Cu-based electrocatalysts to scale up electrochemical CO reduction for high value-added products.
使用合理设计的铜基电催化剂进行电化学CO还原是一种减少CO排放并生产增值产品的有前途的方法。催化剂内部的晶界和微应变已被认为是活性催化位点,而这些位点的可控形成仍然极具挑战性。在这项工作中,我们开发了一种通过液氮快速冷却在CuO电催化剂内部创建高密度晶界和微应变的策略。与冷却速率较慢的样品相比,快速冷却的CuO在其晶畴尺寸、微应变密度以及CO和CO的化学吸附能力方面表现出明显差异。这种富含微应变的CuO电催化剂在相对于可逆氢电极-1.0 V时表现出超过300 mA·cm的高总电流密度以及对C产物(大部分为乙醇)的出色法拉第效率。我们的工作提出了一种调整铜基电催化剂内部晶界和微应变以扩大电化学CO还原以生产高附加值产品的简便方法。