Phase-Regulatable Synthesis of Single-Atom Alloy Nanocages for Efficient Alkaline Hydrogen Evolution

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Wenbin Jiang, , , Song Lin Zhang, , , Jing Yang, , , Shengnan Hu, , , Delong Duan, , , Jerry Zhi Xiong Heng, , , Ziyu Wang, , , Weiwei Yang, , , Xinyang Liu, , , Qingdian Yan, , , Mingsheng Zhang, , , Wen-Ya Wu, , , Jingcong Hu, , , Jiakai Li, , , Ning Ding, , , Siew Lang Teo, , , Chui Yu Chan, , , Ming Lin, , , Hong Liu, , , Xian Jun Loh, , , Yong-Wei Zhang*, , , Zhaolin Liu*, , , Enyi Ye*, , , Yujie Xiong*, , and , Ming Zhao*, 
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引用次数: 0

Abstract

Crystal phase engineering of metal nanocatalysts presents a promising strategy to modulate the catalyst–adsorbate interaction for enhanced catalysis. However, conventional synthetic methods have faced substantial challenges in achieving regulatable crystal phases and lack precise control over catalyst composition at the atomic level, which is detrimental, especially for reactions involving multiple intermediates. Here, we report a facile strategy for simultaneously regulating the crystal phase and composition (Pt single-atom alloying) of ultrathin Ru nanocages (<2 nm in thickness), enabling efficient hydrogen evolution reaction (HER) in alkaline electrolytes. In situ characterizations and theoretical calculations reveal that both the metastable face-centered cubic (fcc) Ru phase and isolated Pt atoms contribute to stabilizing metallic Ru, facilitating Pt–Ru synergy for optimized adsorption of H* and *OH intermediates and accelerated HER kinetics. Consequently, the Pt–Rufcc single-atom alloy nanocages exhibit impressive alkaline HER performance, with an overpotential as low as 8.5 mV at 10 mA cm–2, an 18.0-fold enhancement in mass activity relative to commercial Pt/C and commendable stability over 400 h of operation at ampere-level current densities. This work provides insights into the atomic-level design and preparation of metal nanocrystals with unconventional phases for advanced catalysts.

Abstract Image

用于高效碱氢析氢的单原子合金纳米笼的相位可调合成。
金属纳米催化剂的晶相工程是一种很有前途的调节催化剂-吸附物相互作用以增强催化的方法。然而,传统的合成方法在实现可调节的晶体相方面面临着巨大的挑战,并且在原子水平上缺乏对催化剂组成的精确控制,这是有害的,特别是对于涉及多个中间体的反应。在这里,我们报告了一种简单的策略,可以同时调节超薄Ru纳米笼(厚度< 2nm)的晶相和组成(Pt单原子合金化),从而在碱性电解质中实现高效的析氢反应(HER)。原位表征和理论计算表明,介稳面心立方(fcc) Ru相和分离的Pt原子都有助于稳定金属Ru,促进Pt-Ru协同作用,优化H*和*OH中间体的吸附,加速HER动力学。因此,Pt- rufcc单原子合金纳米笼表现出令人印象深刻的碱性HER性能,在10 mA cm-2时过电位低至8.5 mV,质量活性相对于商用Pt/C提高了18.0倍,并且在安培级电流密度下运行400小时以上的稳定性值得称赞。这项工作为先进催化剂的非常规相金属纳米晶体的原子级设计和制备提供了见解。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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