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磷化钴负载单原子铂催化剂用于氨硼烷水解高效稳定产氢

Cobalt Phosphide-Supported Single-Atom Pt Catalysts for Efficient and Stable Hydrogen Generation from Ammonia Borane Hydrolysis.

作者信息

Wang Shiqi, Li Songqi, Yu Yicheng, Zhang Tianjun, Qu Jiafu, Sun Qiming

机构信息

Innovation Center for Chemical Sciences, College of Chemistry, Chemical Engineering and Materials Science, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, Suzhou, 215123, P. R. China.

School of Materials Science and Engineering, Suzhou University of Science and Technology, Suzhou, 215009, P. R. China.

出版信息

Small Methods. 2024 Dec;8(12):e2400376. doi: 10.1002/smtd.202400376. Epub 2024 May 27.

DOI:10.1002/smtd.202400376
PMID:38801007
Abstract

Ammonia borane (AB) has emerged as a promising chemical hydrogen storage material. The development of efficient, stable, and cost-effective catalysts for AB hydrolysis is the key to achieving hydrogen energy economy. Here, cobalt phosphide (CoP) is used to anchor single-atom Pt species, acting as robust catalysts for hydrogen generation from AB hydrolysis. Thanks to the high Pt utilization and the synergy between CoP and Pt species, the optimized Pt/CoP-100 catalyst exhibits an unprecedented hydrogen generation rate, giving a record turnover frequency (TOF) value of 39911 and turnover number of 2926829 at room temperature. These metrics surpass those of all existing state-of-the-art supported metal catalysts by an order of magnitude. Density functional theory calculations reveal that the integration of single-atom Pt onto the CoP substrate significantly enhances adsorption and dissociation processes for both water and AB molecules, thereby facilitating hydrogen production from AB hydrolysis. Interestingly, the TOF value is further elevated to 54878 under UV-vis light irradiation, which can be attributed to the efficient separation and mobility of photogenerated carriers at the Pt-CoP interface. The findings underscore the effectiveness of CoP as a support for single-atom metals in hydrogen production, offering insights for designing high-performance catalysts for chemical hydrogen storage.

摘要

氨硼烷(AB)已成为一种很有前景的化学储氢材料。开发用于AB水解的高效、稳定且经济高效的催化剂是实现氢能经济的关键。在此,磷化钴(CoP)用于锚定单原子Pt物种,作为AB水解制氢的稳健催化剂。由于Pt的高利用率以及CoP与Pt物种之间的协同作用,优化后的Pt/CoP-100催化剂展现出前所未有的产氢速率,在室温下给出了创纪录的周转频率(TOF)值39911以及周转数2926829。这些指标比所有现有的先进负载型金属催化剂高出一个数量级。密度泛函理论计算表明,单原子Pt整合到CoP基底上显著增强了水和AB分子的吸附和解离过程,从而促进了AB水解制氢。有趣的是,在紫外-可见光照射下,TOF值进一步提高到54878,这可归因于光生载流子在Pt-CoP界面处的有效分离和迁移。这些发现强调了CoP作为单原子金属载体在制氢方面的有效性,为设计用于化学储氢的高性能催化剂提供了见解。

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