Liang Qirui, Li Qizhen, Xie Lei, Zeng Hui, Zhou Shan, Huang Yanan, Yan Miao, Zhang Xin, Liu Tianyi, Zeng Jie, Liang Kang, Terasaki Osamu, Zhao Dongyuan, Jiang Lei, Kong Biao
Laboratory of Advanced Materials, Department of Chemistry, Shanghai Key Lab of Molecular Catalysis and Innovative Materials, iChEM (Collaborative Innovation Centre of Chemistry for Energy Materials), Fudan University, Shanghai 200438, PR China.
School of Materials, University of Manchester, Manchester M13 9PL, United Kingdom.
ACS Nano. 2022 May 24;16(5):7993-8004. doi: 10.1021/acsnano.2c00901. Epub 2022 Apr 8.
Hydrogen evolution reaction (HER) through water splitting is a potential technology to realize the sustainable production of hydrogen, yet the tardy water dissociation and costly Pt-based catalysts inhibit its development. Here, a trapping-bonding strategy is proposed to realize the superassembly of surface-enriched Ru nanoclusters on a phytic acid modified nitrogen-doped carbon framework (denoted as NCPO-Ru NCs). The modified framework has a high affinity to metal cations and can trap plenty of Ru ions. The trapped Ru ions are mainly distributed on the surface of the framework and can form Ru nanoclusters at 50 °C with the synergistic effect of vacancies and phosphate groups. By adjusting the content of phytic acid, surface-enriched Ru nanoclusters with adjustable distribution and densities can be obtained. Benefiting from the adequate exposure of the active sites and dense distribution of ultrasmall Ru nanoclusters, the obtained NCPO-Ru NCs catalyst can effectively drive HER in alkaline electrolytes and show an activity (at overpotential of 50 mV) about 14.3 and 9.6 times higher than that of commercial Ru/C and Pt/C catalysts, respectively. Furthermore, the great performance in solar to hydrogen generation through water splitting provides more flexibility for wide applications of NCPO-Ru NCs.
通过水分解产生氢气的反应(HER)是实现可持续制氢的一种潜在技术,然而缓慢的水离解和昂贵的铂基催化剂阻碍了其发展。在此,提出了一种捕获-键合策略,以实现富含表面的钌纳米团簇在植酸修饰的氮掺杂碳骨架(表示为NCPO-Ru NCs)上的超组装。修饰后的骨架对金属阳离子具有高亲和力,能够捕获大量的钌离子。捕获的钌离子主要分布在骨架表面,并在50℃下通过空位和磷酸基团的协同作用形成钌纳米团簇。通过调节植酸的含量,可以获得分布和密度可调的富含表面的钌纳米团簇。受益于活性位点的充分暴露和超小钌纳米团簇的密集分布,所制备的NCPO-Ru NCs催化剂能够在碱性电解质中有效地驱动析氢反应,并且在过电位为50 mV时的活性分别比商业Ru/C和Pt/C催化剂高约14.3倍和9.6倍。此外,通过水分解实现太阳能制氢的优异性能为NCPO-Ru NCs的广泛应用提供了更大的灵活性。