Dynamic Surface Pre-reconstruction and Selenization Co-regulate the Electronic Structure of the Central Metal Ni and Promote the Efficient Water-splitting

IF 12.1 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-07-01 DOI:10.1002/smll.202502805
Qiuyan Chen, Changxue Dong, Jie Zhang, Gang Wang, Ruilin Wang, Jinwei Chen
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Abstract

In the oxygen evolution reaction (OER), it is discovered that introducing defects into Ni-based electrocatalysts can effectively enhance their catalytic activity. However, the specific structure of these defects and their role in modulating the performance of electrocatalysts remain unclear. Herein, an innovative core-shell nano-heterogeneous catalyst is reported that significantly boosts water decomposition efficiency through a strategy combining dynamic surface pre-reconfiguration and selenization. The Ni3Mo-reconstruction@MoSe2/NiSe2 (NM-Re@MS/NS) core-shell heterogeneous catalyst is designed and synthesized. The surface pre-reconstruction technique is employed to adjust the element distribution and induce the catalyst to form a more active surface phase. The MoSe2/NiSe2 (MS/NS) modulates the electronic structure and surface chemistry of the catalyst, thereby facilitating the adsorption/desorption of OH⁻ and *H. As anticipated, NM-Re@MS/NS exhibited excellent catalytic activity for both the OER and hydrogen evolution reaction (HER) in 1.0 M KOH (OER: 258 mV@300 mA cm⁻2; HER: 65 mV@10 mA cm⁻2), with notable stability (OER: 80 h@250 mA cm⁻2; HER: 63h@250 mA cm⁻2). Importantly, in OER || HER system, the NM-Re@MS/NS catalyst, acting as both cathode and anode, exhibits an overpotential of 284 mV at 300 mA cm⁻2, significantly increasing the rates of hydrogen and oxygen production.

Abstract Image

动态表面预重构和硒化Co -调节中心金属Ni的电子结构,促进高效的水分解
在析氧反应(OER)中,发现在Ni基电催化剂中引入缺陷可以有效地提高其催化活性。然而,这些缺陷的具体结构及其在调节电催化剂性能中的作用尚不清楚。本文报道了一种创新的核-壳纳米非均相催化剂,通过结合动态表面预重构和硒化策略,显著提高了水分解效率。设计并合成了Ni3Mo‐reconstruction@MoSe2/NiSe2 (NM‐Re@MS/NS)核壳异相催化剂。采用表面预重构技术调整元素分布,诱导催化剂形成更活跃的表面相。MoSe2/ nis2 (MS/NS)调节催化剂的电子结构和表面化学,从而促进OH -和*H的吸附/解吸。正如预期的那样,NM‐Re@MS/NS在1.0 M KOH (OER: 258 mV@300 mA cm⁻2;HER: 65 mV@10 mA cm - 2),具有显著的稳定性(OER: 80 h@250 mA cm - 2;她:63h@250 mA cm(2)。重要的是,在OER || HER系统中,NM‐Re@MS/NS催化剂作为阴极和阳极,在300 mA cm⁻2下表现出284 mV的过电位,显著提高了氢和氧的生成速率。
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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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