Deliberate Amorphization of Co-MOF for Constructing Crystalline-Amorphous Heterostructures Toward High-Performance Water Electrolysis

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2024-09-18 DOI:10.1002/smll.202404598
Guangyao Zhou, Xue Zhou, Jing Li, Weiran Huang, Huan Pang, Songtao Zhang, Jun Yang, Lin Xu, Yawen Tang
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Abstract

The endowment of metal organic frameworks (MOF) with superior electrocatalytic performance without compromising their structural/compositional superiorities is of great significance for the development of renewable energy devices, yet remains a grand challenge. Herein, a deliberate partial amorphization strategy is developed to construct a heterostructured electrocatalyst consisting of crystalline Co-MOF and amorphous Co-S nanoflake arrays aligned on the carbon cloth (CC) substrate (abbreviated as Co-MOF/Co-S@CC hereafter) through a rapid sulfuration method. The simultaneous implement of crystalline-amorphous (c-a) heterostructure and nanoflake arrayed architecture on CC substrate renders the Co-MOF/Co-S@CC with abundant and tight active sites, accelerated charge transfer rate, regulated electronic structures, and reinforced structural stability. As such, the obtained Co-MOF/Co-S@CC electrode demonstrates outstanding electrochemical hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performances with the overpotentials of 64 and 217 mV at 10 mA cm−2, respectively. Moreover, a two-electrode electrolyzer assembled by Co-MOF/Co-S@CC electrodes exhibits the lower cell voltages and larger current densities than those of Pt/C and RuO2 counterparts, excellent reversibility and prominent long-term stability, representing a great prospect for feasible H2 production. This adopted concept of c-a heterostructure for electronic regulation may bring about insightful inspiration for designing high-performance electrocatalysts for sustainable energy systems.

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故意使 Co-MOF 非晶化,以构建晶体-非晶异质结构,实现高性能水电解
赋予金属有机框架(MOF)卓越的电催化性能,同时又不损害其结构/组成的优越性,这对可再生能源设备的开发意义重大,但仍然是一个巨大的挑战。本文开发了一种有意的部分非晶化策略,通过快速硫化法构建了一种异质结构的电催化剂,该催化剂由结晶 Co-MOF 和排列在碳布(CC)基底上的非晶 Co-S 纳米片阵列组成(以下简称 Co-MOF/Co-S@CC)。在碳布基底上同时实现晶体-非晶(c-a)异质结构和纳米片阵列结构,使 Co-MOF/Co-S@CC 具有丰富而紧密的活性位点,加快了电荷转移速率,调节了电子结构,并增强了结构稳定性。因此,所获得的 Co-MOF/Co-S@CC 电极具有出色的电化学氢进化反应(HER)和氧进化反应(OER)性能,在 10 mA cm-2 条件下的过电位分别为 64 mV 和 217 mV。此外,Co-MOF/Co-S@CC 电极组装的双电极电解槽与 Pt/C 和 RuO2 电极相比,具有更低的电池电压和更大的电流密度、优异的可逆性和突出的长期稳定性,为可行的 H2 生产提供了广阔的前景。这种采用c-a异质结构进行电子调节的概念可能会为设计用于可持续能源系统的高性能电催化剂带来深刻的启发。
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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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