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用于低浓度乙炔电化学还原为乙烯并抑制析氢的二氧化钛负载铜单原子催化剂

Titania-Supported Cu-Single-Atom Catalyst for Electrochemical Reduction of Acetylene to Ethylene at Low-Concentrations with Suppressed Hydrogen Evolution.

作者信息

Wang Zeping, Shang Lu, Yang Hongzhou, Zhao Yunxuan, Waterhouse Geoffrey I N, Li Dong, Shi Run, Zhang Tierui

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Adv Mater. 2023 Oct;35(42):e2303818. doi: 10.1002/adma.202303818. Epub 2023 Sep 11.

Abstract

Electrochemical acetylene reduction (EAR) is a promising strategy for removing acetylene from ethylene-rich gas streams. However, suppressing the undesirable hydrogen evolution is vital for practical applications in acetylene-insufficient conditions. Herein, Cu single atoms are immobilized on anatase TiO nanoplates (Cu-SA/TiO ) for electrochemical acetylene reduction, achieving an ethylene selectivity of ≈97% with a 5 vol% acetylene gas feed (Ar balance). At the optimal Cu-single-atom loading, Cu-SA/TiO is able to effectively suppress HER and ethylene over-hydrogenation even when using dilute acetylene (0.5 vol%) or ethylene-rich gas feeds, delivering a 99.8% acetylene conversion, providing a turnover frequency of 8.9 × 10  s , which is superior to other EAR catalysts reported to date. Theoretical calculations show that the Cu single atoms and the TiO support acted cooperatively to promote charge transfer to adsorbed acetylene molecules, whilst also inhibiting hydrogen generation in alkali environments, thus allowing selective ethylene production with negligible hydrogen evolution at low acetylene concentrations.

摘要

电化学乙炔还原(EAR)是一种从富含乙烯的气流中去除乙炔的有前景的策略。然而,在乙炔不足的条件下,抑制不希望的析氢反应对于实际应用至关重要。在此,铜单原子固定在锐钛矿型TiO纳米片(Cu-SA/TiO)上用于电化学乙炔还原,在进料为5 vol%乙炔气体(氩气平衡)时实现了约97%的乙烯选择性。在最佳铜单原子负载量下,即使使用稀乙炔(0.5 vol%)或富含乙烯的气体进料,Cu-SA/TiO也能够有效抑制析氢反应和乙烯过度氢化,实现99.8%的乙炔转化率,周转频率为8.9×10⁻³ s⁻¹,优于迄今报道的其他EAR催化剂。理论计算表明,铜单原子与TiO载体协同作用,促进电荷转移至吸附的乙炔分子,同时抑制碱性环境中的氢气生成,从而在低乙炔浓度下以可忽略不计的析氢反应实现选择性乙烯生成。

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