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一种用于室温下将甲醛水溶液高效转化为氢气的铜镍合金-碳层核壳催化剂。

A CuNi Alloy-Carbon Layer Core-Shell Catalyst for Highly Efficient Conversion of Aqueous Formaldehyde to Hydrogen at Room Temperature.

作者信息

Zhou Zining, Ng Yun Hau, Xu Shengju, Yang Siyuan, Gao Qiongzhi, Cai Xin, Liao Jihai, Fang Yueping, Zhang Shengsen

机构信息

Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou 510643, China.

School of Energy and Environment, City University of Hong Kong, Hong Kong 999077, China.

出版信息

ACS Appl Mater Interfaces. 2021 Aug 11;13(31):37299-37307. doi: 10.1021/acsami.1c11776. Epub 2021 Jul 29.

DOI:10.1021/acsami.1c11776
PMID:34324293
Abstract

A copper (Cu) material is catalytically active for formaldehyde (HCHO) dehydrogenation to produce H, but the unsatisfactory efficiency and easy corrosion hinder its practical application. Alloying with other metals and coating a carbon layer outside are recognized as effective strategies to improve the catalytic activity and the long-term durability of nonprecious metal catalysts. Here, highly dispersed CuNi alloy-carbon layer core-shell nanoparticles (CuNi@C) have been developed as a robust catalyst for efficient H generation from HCHO aqueous solution at room temperature. Under the optimized reaction conditions, the CuNi@C catalyst exhibits a H evolution rate of 110.98 mmol·h·g, which is 1.5 and 4.9 times higher than those of Cu@C and Ni@C, respectively, which ranks top among the reported nonprecious metal catalysts for catalytic HCHO reforming at room temperature to date. Furthermore, CuNi@C also displays excellent stability toward the catalytic HCHO reforming into H in tap water owing to the well-constructed carbon sheath protecting CuNi nanocrystals from oxidation in an alkaline medium. Combined with density functional theory calculations, the superior catalytic efficiency of CuNi@C for H generation results from the synergistic contribution between the massive active species from HCHO decomposition on the Cu sites and the remarkable H evolution activity on Ni sites. The improved performance of CuNi@C highlights the enormous potential of advancing noble-metal-free nanoalloys as cost-effective and recyclable catalysts for energy recovery from industrial HCHO wastewater.

摘要

铜(Cu)材料对甲醛(HCHO)脱氢生成氢气具有催化活性,但效率不理想且易腐蚀,阻碍了其实际应用。与其他金属合金化以及在外部包覆碳层被认为是提高非贵金属催化剂催化活性和长期耐久性的有效策略。在此,高度分散的CuNi合金-碳层核壳纳米颗粒(CuNi@C)已被开发为一种强大的催化剂,用于在室温下从甲醛水溶液中高效产氢。在优化的反应条件下,CuNi@C催化剂的析氢速率为110.98 mmol·h·g,分别比Cu@C和Ni@C高1.5倍和4.9倍,在迄今为止报道的用于室温催化HCHO重整的非贵金属催化剂中排名第一。此外,由于构建良好的碳鞘保护CuNi纳米晶体在碱性介质中不被氧化,CuNi@C在自来水中对催化HCHO重整为H也表现出优异的稳定性。结合密度泛函理论计算,CuNi@C对产氢的卓越催化效率源于Cu位点上HCHO分解产生的大量活性物种与Ni位点上显著的析氢活性之间的协同作用。CuNi@C性能的提升突出了推进无贵金属纳米合金作为从工业HCHO废水中回收能量的经济高效且可回收催化剂的巨大潜力。

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