Ji Yujing, Wu Jichuang, Lee Ha Eun, An Yongsu, Jung Duk-Young, Lee Chan Woo, Kim Young Dok, Seo Hyun Ook
Department of Chemistry, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Department of Chemistry and Energy Engineering, Sangmyung University, Seoul 03016, Republic of Korea.
ACS Omega. 2024 Nov 26;9(49):48855-48866. doi: 10.1021/acsomega.4c09642. eCollection 2024 Dec 10.
Two types of bismuth films (micro-Bi and nano-Bi) were prepared, and their electrocatalytic behavior was studied in terms of reduction current and product selectivity in a potential range of -0.776 to -1.376 V vs RHE. CO and HO molecules competed with each other for reduction on the surfaces of both types of films, and formate and H were the respective major products of reductive reactions. Under the same conditions, nano-Bi exhibited lower selectivity for formate and higher selectivity for H compared to the respective micro-Bi cases with bismuth films of similar thickness. This can be attributed to the higher hydrophilicity of bismuth film surfaces of nano-Bi due to surface nanoscale roughness and lower surface-carbon content compared with those of micro-Bi. Our results suggest a new strategy for controlling the selectivity of electrocatalytic CO reduction under aqueous electrolytes through the use of surface engineering.
制备了两种铋膜(微米级铋和纳米级铋),并在相对于可逆氢电极(RHE)为-0.776至-1.376 V的电位范围内,根据还原电流和产物选择性研究了它们的电催化行为。CO和H₂O分子在两种膜表面相互竞争还原反应,甲酸盐和H₂分别是还原反应的主要产物。在相同条件下,与具有相似厚度铋膜的微米级铋相比,纳米级铋对甲酸盐的选择性较低,对H₂的选择性较高。这可归因于纳米级铋的铋膜表面由于表面纳米级粗糙度而具有更高的亲水性,且与微米级铋相比表面碳含量更低。我们的结果表明了一种通过表面工程控制水性电解质下电催化CO还原选择性的新策略。