Dynamic Surface Pre-reconstruction and Selenization Co-regulate the Electronic Structure of the Central Metal Ni and Promote the Efficient Water-splitting
Qiuyan Chen, Changxue Dong, Jie Zhang, Gang Wang, Ruilin Wang, Jinwei Chen
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引用次数: 0
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.
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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