Laboratory of Advanced Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Center of Chemistry for Energy Materials, Fudan University, Shanghai 200438, China.
Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
J Colloid Interface Sci. 2018 Dec 1;531:564-569. doi: 10.1016/j.jcis.2018.07.066. Epub 2018 Jul 20.
The increasing accumulation of CO in the atmosphere has been leading to serious environmental problems. Electrochemical reduction of CO is a potential means of carbon recycling for energy storage and environmental sustainability. However, it is limited by the lack of highly active and selective electrocatalysts. Here we demonstrate the development of mesoporous tin oxide (SnO) for electrocatalytic CO reduction, which facilitates the adsorption and electrochemical reduction of CO inside mesopores. The highly-ordered and uniform pore sizes of the mesoporous SnO electrocatalyst favor the enhancement of formation of carbon monoxide (CO) and formate during the electrochemical reduction. The combined faradaic efficiencies of CO and formate reach a peak value of ∼80% at a current density of 5 mA cm at -0.8 V vs. reversible hydrogen electrode. This work suggests attractive development of mesoporous electrocatalysts with a variety of pore size and structures for efficient energy conversion and electrochemical CO reduction.
大气中 CO 的不断积累导致了严重的环境问题。电化学还原 CO 是一种用于储能和环境可持续性的碳循环的潜在手段。然而,它受到缺乏高活性和选择性电催化剂的限制。在这里,我们展示了介孔氧化锡(SnO)在电催化 CO 还原方面的开发,这有利于 CO 在介孔内的吸附和电化学还原。介孔 SnO 电催化剂的高度有序和均匀的孔径有利于增强在电化学还原过程中一氧化碳(CO)和甲酸盐的形成。在-0.8 V 相对于可逆氢电极的电流密度为 5 mA cm 时,CO 和甲酸盐的总法拉第效率达到约 80%的峰值。这项工作为具有各种孔径和结构的介孔电催化剂的有效能量转换和电化学 CO 还原提供了有吸引力的发展方向。