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源自β-BiO的多孔铋纳米片用于高效电催化将CO还原为甲酸盐。

Porous Bi Nanosheets Derived from β-BiO for Efficient Electrocatalytic CO Reduction to Formate.

作者信息

Pang Yongyu, Xie Ruikuan, Xie Huan, Lan Shaojie, Jiang Taiwen, Chai Guoliang

机构信息

Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou, Fujian 350108, People's Republic of China.

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences (CAS), Fuzhou, Fujian 350002, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 14;16(32):42109-42117. doi: 10.1021/acsami.4c05842. Epub 2024 Aug 1.

DOI:10.1021/acsami.4c05842
PMID:39088819
Abstract

The electrochemical CO reduction reaction (ECORR) is a promising strategy for converting CO into high-value chemical products. However, the synthesis of effective and stable electrocatalysts capable of transforming CO into a specified product remains a huge challenge. Herein, we report a template-regulated strategy for the preparation of a BiO-derived nanosheet catalyst with abundant porosity to achieve the expectantly efficient CO-to-formate conversion. The resultant porous bismuth nanosheet (-Bi) not only exhibited marked Faradaic efficiency of formate (), beyond 91% in a broad potential range from -0.75 to -1.1 V in the H-type cell, but also demonstrated an appreciable of 94% at a high current density of 262 mA cm in the commercially important gas diffusion cell. State-of-the-art X-ray absorption near edge structure spectroscopy (XANES) and theoretical calculation unraveled the distinct formate production performance of the -Bi catalyst, which was cocontributed by its smaller size, plentiful porous structure, and stronger Bi-O bond, thus accelerating the absorption of CO and promoting the subsequent formation of intermediates. This work provides an avenue to fabricate bismuth-based catalysts with high planar and porous morphologies for a broad portfolio of applications.

摘要

电化学CO还原反应(ECORR)是将CO转化为高价值化学产品的一种有前景的策略。然而,合成能够将CO转化为特定产物的有效且稳定的电催化剂仍然是一个巨大的挑战。在此,我们报道了一种模板调控策略,用于制备具有丰富孔隙率的BiO衍生纳米片催化剂,以实现预期的高效CO到甲酸盐的转化。所得的多孔铋纳米片(-Bi)不仅在H型电池中-0.75至-1.1 V的宽电位范围内表现出显著的甲酸盐法拉第效率(),超过91%,而且在商业上重要的气体扩散电池中,在262 mA cm的高电流密度下也表现出可观的94%的。先进的X射线吸收近边结构光谱(XANES)和理论计算揭示了-Bi催化剂独特的甲酸盐生成性能,这是由其较小的尺寸、丰富的多孔结构和更强的Bi-O键共同促成的,从而加速了CO的吸收并促进了随后中间体的形成。这项工作为制备具有高平面和多孔形态的铋基催化剂以用于广泛的应用提供了一条途径。

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