原位活化诱导cr - Ni3S2表面重构增强碱性析氢反应

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Ruidi Li, Cong Chen, Junxia Shen, Zhihe Wei, Pierre-Yves Olu, Wen Dong, Yang Peng, Ronglei Fan and Mingrong Shen
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引用次数: 0

摘要

Ni3S2因其温和的活性、优异的导电性和可扩展的方法而成为最有前途的析氢反应(HER)催化剂之一,然而,H2O解离的高能量势垒和H*中间体的弱解吸严重阻碍了其析氢反应动力学。本研究采用一步电沉积法在Ni网基板(Cr-Ni3S2/NM)上生长了一种新型的Cr-Ni3S2,该材料具有较大的表面积和丰富的Ni3S2/Cr2S3异质结。因此,原位活化后的表面重构(记为a - cr - ni3s2 /NM)不仅增强了电荷和传质,还通过在催化剂表面引入更多的氧和S空位改变了电子结构。理论计算表明,原位活化不仅促进了电荷输运,而且通过加强OH*对H2O解离的脱附和促进H*中间体的脱附,提高了HER动力学。结果表明,制备的a - cr - ni3s2 /NM具有优异的HER性能,过电位为78 mV,电流密度为-10 mA/cm2,在100 mA/cm2下稳定性超过200小时。表面重构已经在析氧反应催化剂上得到了深入的研究,而我们在本研究中也证明了它在Cr-Ni3S2 HER催化剂上也发挥了巨大的积极作用,从而为实现高性能HER催化剂提供了一条途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In situ activation-induced surface reconstruction on Cr-incorporated Ni3S2 for enhanced alkaline hydrogen evolution reaction†

In situ activation-induced surface reconstruction on Cr-incorporated Ni3S2 for enhanced alkaline hydrogen evolution reaction†

Ni3S2 has emerged as one of the most promising hydrogen evolution reaction (HER) catalysts due to its moderate activity, exceptional electrical conductivity, and scalable synthesis methods. However, the high energy barrier for H2O dissociation and weak desorption of the H* intermediate severely hinder its HER kinetics. In this study, a novel Cr-incorporated Ni3S2 was grown on a Ni mesh substrate (denoted as Cr–Ni3S2/NM) using a one-step electrodeposition approach, resulting in a large surface area with abundant Ni3S2/Cr2S3 heterojunctions. Subsequently, it underwent surface reconstruction after in situ activation (denoted as A–Cr–Ni3S2/NM), which not only enhanced charge and mass transfer but also altered the electronic structure by introducing more oxygen species on the catalyst surface and creating S vacancies. Using theoretical calculations, this in situ activation was shown to not only promote charge transport but also boost HER kinetics by strengthening OH* desorption for H2O dissociation and facilitating the desorption of H* intermediates. As a result, the fabricated A–Cr–Ni3S2/NM demonstrated exceptional HER performance with a small overpotential of 78 mV to deliver a current density of −10 mA cm−2, along with stability for over 200 h at 100 mA cm−2. While surface reconstruction has been intensively studied in catalysts for the oxygen evolution reaction, we illustrate that it also plays a significant and positive role in Cr–Ni3S2 HER catalysts in this study, thus providing a pathway for achieving high-performance HER catalysts.

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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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