格式化
电催化剂
氧化锡
电解
纳米颗粒
甲酸脱氢酶
法拉第效率
材料科学
化学工程
无机化学
纳米晶材料
欧姆接触
化学
甲醇
电化学
催化作用
氧化物
甲酸
锡
核化学
纳米技术
电极
冶金
有机化学
电解质
物理化学
图层(电子)
工程类
作者
Ivan Merino-Garcia,Lionel Tinat,Jonathan Albo,Manuel Alvarez-Guerra,Angel Irabien,Olivier Durupthy,Vincent Vivier,Carlos Sánchez-Sánchez
标识
DOI:10.1016/j.apcatb.2021.120447
摘要
• Synthesis of high surface area SnO 2 NPs as electrocatalyst for continuous production of formate from CO 2 RR. • First evaluation of 2 nm SnO 2 NPs performance for CO 2 RR in a flow electrolyzer. • A maximum [formate] of 27 g L −1 was achieved with a FE of 44.9 % at 300 mA cm -2 . • [formate] of 27 g L −1 provokes a significant formate migration current. Tin oxide nanoparticles (SnO 2 NPs) as electrocatalyst for the production of formate from CO 2 reduction reaction (CO 2 RR). We synthesize, characterize and evaluate high surface area SnO 2 NPs (2.4 nm and 299 m 2 g −1 in diameter size and surface area, respectively), for the continuous production of formate at high current density within a flow electrolyzer. SnO 2 NPs under Ar and CO 2 reduction conditions were studied by cyclic voltammetry. SnO 2 -based gas diffusion electrodes (SnO 2 -GDEs) were manufactured to perform continuous CO 2 RR. A maximum formate concentration value of 27 g L −1 was achieved with a Faradaic efficiency (FE) of 44.9 % at 300 mA cm -2 , which was significantly stable and reproducible when operated up to 10 h. Nevertheless, ohmic drop contribution due to the semiconducting properties of SnO 2 was not negligible. The low total FE (< 60 %) of products pointed out a leakage of formate by crossover migration through the membrane from the catholyte towards the anolyte.
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