Deep Reconstruction of RuPdOx Hollow Nanofibers for Efficient Electrocatalytic Hydrazine Oxidation-Assisted Hydrogen Production

IF 27.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yuezhu Wang, Qiuling Jiang, Siyu Ren, Jiaqi Xu, Ying Wang, Mengxiao Zhong, Xiaofeng Lu
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Abstract

Manipulating the reconstruction of a heterostructured material is highly desirable to achieve high-performance electrocatalytic performance. Here, an in situ reconstruction of RuPdOx hollow nanofibers (HNFs) is presented to generate RuO2/Pd from both the electrochemical and chemical reconstruction processes. The reconstructed catalyst is highly efficient for both hydrazine oxidation reaction (HzOR) and hydrogen evolution reaction (HER) at industrial-grade current densities, significantly outperforming the benchmark Pt/C catalyst. Furthermore, it maintains a record-breaking durability of 500 h for HzOR at 1 A cm−2. Remarkably, with the catalyst as electrodes, a two-electrode overall hydrazine splitting (OHzS) cell is constructed, which requires only 0.263 kWh of electricity to produce 1 m3 H2 at 100 mA cm−2, significantly lower than that in overall water splitting (OWS) system (4.286 kWh m−3 H2), exhibiting an exceptional energy-saving H2 production property. Density functional theory (DFT) calculations reveal an efficient electron transfer from Pd to RuO2 at their interface from the reconstruction of RuPdOx HNFs, which regulates the local electronic environment of atoms, modulates the adsorption and desorption for intermediates, and reduces the energy barriers for enhancing the electrocatalytic process. This study offers a robust reconstruction strategy for the design of electrocatalysts that exhibit superior efficiency in energy conversion devices.

Abstract Image

用于高效电催化肼氧化辅助制氢的RuPdOx中空纳米纤维的深度重构
操纵异质结构材料的重构是实现高性能电催化性能的迫切需要。本文提出了一种RuPdOx空心纳米纤维(HNFs)的原位重建方法,通过电化学和化学重建过程生成RuO2/Pd。在工业级电流密度下,重构的催化剂在肼氧化反应(HzOR)和析氢反应(HER)中都具有很高的效率,显著优于基准Pt/C催化剂。此外,它在1 a cm−2的高压下保持了500小时的破纪录耐久性。值得注意的是,以催化剂为电极,构建了双电极整体联氨分解(OHzS)电池,在100 mA cm−2下产生1 m3 H2仅需0.263 kWh的电力,显著低于整体水分解(OWS)系统(4.286 kWh m−3 H2),表现出卓越的节能制氢性能。密度泛函理论(DFT)计算表明,重构的RuPdOx hnf在其界面上实现了从Pd到RuO2的有效电子转移,从而调节了原子的局部电子环境,调节了中间体的吸附和解吸,降低了增强电催化过程的能量障碍。本研究为设计在能量转换装置中表现出卓越效率的电催化剂提供了强有力的重构策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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