Yuan Ma , Chunhong Li , Muhammad Aizaz Ud Din , Lan Zhao , Nengcong Pan , Yuhan Lei , Nanpu Cheng
{"title":"fe掺杂CoSe2纳米片作为水裂解析氧反应的有效电催化剂","authors":"Yuan Ma , Chunhong Li , Muhammad Aizaz Ud Din , Lan Zhao , Nengcong Pan , Yuhan Lei , Nanpu Cheng","doi":"10.1016/j.jallcom.2025.182600","DOIUrl":null,"url":null,"abstract":"<div><div>Affordable and highly effective electrocatalysts are essential for achieving industrial-scale hydrogenation of water applications. The successful fabrication of Fe-doped CoSe<sub>2</sub> nanosheets supported on nickel foam (Fe<sub>x</sub>-CoSe<sub>2</sub>/NF) via a two-step electrochemical deposition method is presented in this study, showing their effectiveness as an electrocatalyst for the oxygen evolution reaction (OER) in water splitting. The performance of Fe<sub>x</sub>-CoSe<sub>2</sub>/NF initially improves with increasing x, reaching an optimal value before subsequently declining. The ideal catalyst, Fe<sub>0.75</sub>-CoSe<sub>2</sub>/NF, requires a low overpotential of 256 mV at 10 mA cm<sup>−2</sup>, and even at 100 mA cm<sup>−2</sup>, the overpotential remains as low as 291 mV. The catalyst also displays a low Tafel slope of 34.37 mV dec<sup>−1</sup>, highlighting the fast OER kinetics. Furthermore, Fe<sub>0.75</sub>-CoSe<sub>2</sub>/NF demonstrates exceptional electrochemical stability. The enhanced OER catalytic performance of Fe-doped CoSe<sub>2,</sub> compared to intrinsic CoSe<sub>2,</sub> is attributed to the thinner nanosheets structure and optimized electronic structures, which provide a higher density of active sites and facilitate a new reaction coordination with a lower energy barrier during the OER process. These findings not only offer new mechanistic insights into Fe-doped CoSe<sub>2</sub> systems but also provide a scalable and cost-effective pathway for designing next-generation, non-precious-metal-based electrocatalysts.</div></div>","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"1038 ","pages":"Article 182600"},"PeriodicalIF":6.3000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fe-doped CoSe2 nanosheets as effective electrocatalysts for the oxygen evolution reaction in water splitting\",\"authors\":\"Yuan Ma , Chunhong Li , Muhammad Aizaz Ud Din , Lan Zhao , Nengcong Pan , Yuhan Lei , Nanpu Cheng\",\"doi\":\"10.1016/j.jallcom.2025.182600\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Affordable and highly effective electrocatalysts are essential for achieving industrial-scale hydrogenation of water applications. The successful fabrication of Fe-doped CoSe<sub>2</sub> nanosheets supported on nickel foam (Fe<sub>x</sub>-CoSe<sub>2</sub>/NF) via a two-step electrochemical deposition method is presented in this study, showing their effectiveness as an electrocatalyst for the oxygen evolution reaction (OER) in water splitting. The performance of Fe<sub>x</sub>-CoSe<sub>2</sub>/NF initially improves with increasing x, reaching an optimal value before subsequently declining. The ideal catalyst, Fe<sub>0.75</sub>-CoSe<sub>2</sub>/NF, requires a low overpotential of 256 mV at 10 mA cm<sup>−2</sup>, and even at 100 mA cm<sup>−2</sup>, the overpotential remains as low as 291 mV. The catalyst also displays a low Tafel slope of 34.37 mV dec<sup>−1</sup>, highlighting the fast OER kinetics. Furthermore, Fe<sub>0.75</sub>-CoSe<sub>2</sub>/NF demonstrates exceptional electrochemical stability. The enhanced OER catalytic performance of Fe-doped CoSe<sub>2,</sub> compared to intrinsic CoSe<sub>2,</sub> is attributed to the thinner nanosheets structure and optimized electronic structures, which provide a higher density of active sites and facilitate a new reaction coordination with a lower energy barrier during the OER process. 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引用次数: 0
摘要
经济实惠、高效的电催化剂对于实现工业规模的水加氢应用至关重要。本文采用两步电化学沉积方法成功制备了泡沫镍负载的fe掺杂CoSe2纳米片(Fex-CoSe2/NF),证明了其作为析氧反应(OER)电催化剂的有效性。Fex-CoSe2/NF的性能最初随着x的增加而提高,达到一个最优值,随后下降。理想的催化剂Fe0.75-CoSe2/NF在10 mA cm-2时需要256 mV的低过电位,即使在100 mA cm-2时,过电位仍然低至291 mV。该催化剂的Tafel斜率为34.37 mV / dec-1,具有较快的OER动力学。此外,Fe0.75-CoSe2/NF表现出优异的电化学稳定性。与本质CoSe2相比,fe掺杂CoSe2的OER催化性能得到了增强,这是由于其更薄的纳米片结构和优化的电子结构,在OER过程中提供了更高的活性位点密度,并促进了以更低的能垒进行新的反应配位。这些发现不仅为fe掺杂CoSe2体系提供了新的机制见解,而且为设计下一代非贵金属基电催化剂提供了可扩展且经济高效的途径。
Fe-doped CoSe2 nanosheets as effective electrocatalysts for the oxygen evolution reaction in water splitting
Affordable and highly effective electrocatalysts are essential for achieving industrial-scale hydrogenation of water applications. The successful fabrication of Fe-doped CoSe2 nanosheets supported on nickel foam (Fex-CoSe2/NF) via a two-step electrochemical deposition method is presented in this study, showing their effectiveness as an electrocatalyst for the oxygen evolution reaction (OER) in water splitting. The performance of Fex-CoSe2/NF initially improves with increasing x, reaching an optimal value before subsequently declining. The ideal catalyst, Fe0.75-CoSe2/NF, requires a low overpotential of 256 mV at 10 mA cm−2, and even at 100 mA cm−2, the overpotential remains as low as 291 mV. The catalyst also displays a low Tafel slope of 34.37 mV dec−1, highlighting the fast OER kinetics. Furthermore, Fe0.75-CoSe2/NF demonstrates exceptional electrochemical stability. The enhanced OER catalytic performance of Fe-doped CoSe2, compared to intrinsic CoSe2, is attributed to the thinner nanosheets structure and optimized electronic structures, which provide a higher density of active sites and facilitate a new reaction coordination with a lower energy barrier during the OER process. These findings not only offer new mechanistic insights into Fe-doped CoSe2 systems but also provide a scalable and cost-effective pathway for designing next-generation, non-precious-metal-based electrocatalysts.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.