Xiaotong Wei , Shucong Zhang , Xingshuai Lv , Shuixing Dai , Huanlei Wang , Minghua Huang
{"title":"局部重构使磷化钴阵列具有氢进化和肼氧化双功能","authors":"Xiaotong Wei , Shucong Zhang , Xingshuai Lv , Shuixing Dai , Huanlei Wang , Minghua Huang","doi":"10.1016/j.apcatb.2023.123661","DOIUrl":null,"url":null,"abstract":"<div><p>Coupling hydrazine electrooxidation with hydrogen evolution reaction (HER) attracts ever-growing attention for energy-saving H<sub>2</sub> production. However, the performance of hydrazine-assisted HER unit is restricted by the bifunctional catalysts with un-fully activated sites. Herein, a surface local-reconstruction strategy is proposed to integrate amorphous Co(OH)<sub>2</sub> and P vacant CoP into the CoH-CoP<sub>V</sub>@CFP catalyst. The inherent electron-deficient Co sites in Co(OH)<sub>2</sub> show strong N-Co interaction to accelerate the N<sub>2</sub>H<sub>4</sub><span> dehydrogenation kinetics, while the as-formed P vacancies in CoP play a crucial role in moderating the H* adsorption energy, the excellent bifunctionality thus being obtained. Specifically, it achieves the low overpotentials of − 77 and − 61 mV at 10 mA cm</span><sup>−2</sup> for HER and HzOR in alkaline media, respectively. A lab-scale electrolyzer can deliver the industrial-grade current density of 500 mA cm<sup>−2</sup> under ultralow cell voltage of 0.23 V. This local-reconstruction strategy may pave new avenue to design efficient catalysts for hydrazine-assisted H<sub>2</sub> generation.</p></div>","PeriodicalId":244,"journal":{"name":"Applied Catalysis B: Environmental","volume":"345 ","pages":"Article 123661"},"PeriodicalIF":20.2000,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Local-reconstruction enables cobalt phosphide array with bifunctional hydrogen evolution and hydrazine oxidation\",\"authors\":\"Xiaotong Wei , Shucong Zhang , Xingshuai Lv , Shuixing Dai , Huanlei Wang , Minghua Huang\",\"doi\":\"10.1016/j.apcatb.2023.123661\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Coupling hydrazine electrooxidation with hydrogen evolution reaction (HER) attracts ever-growing attention for energy-saving H<sub>2</sub> production. However, the performance of hydrazine-assisted HER unit is restricted by the bifunctional catalysts with un-fully activated sites. Herein, a surface local-reconstruction strategy is proposed to integrate amorphous Co(OH)<sub>2</sub> and P vacant CoP into the CoH-CoP<sub>V</sub>@CFP catalyst. The inherent electron-deficient Co sites in Co(OH)<sub>2</sub> show strong N-Co interaction to accelerate the N<sub>2</sub>H<sub>4</sub><span> dehydrogenation kinetics, while the as-formed P vacancies in CoP play a crucial role in moderating the H* adsorption energy, the excellent bifunctionality thus being obtained. Specifically, it achieves the low overpotentials of − 77 and − 61 mV at 10 mA cm</span><sup>−2</sup> for HER and HzOR in alkaline media, respectively. A lab-scale electrolyzer can deliver the industrial-grade current density of 500 mA cm<sup>−2</sup> under ultralow cell voltage of 0.23 V. This local-reconstruction strategy may pave new avenue to design efficient catalysts for hydrazine-assisted H<sub>2</sub> generation.</p></div>\",\"PeriodicalId\":244,\"journal\":{\"name\":\"Applied Catalysis B: Environmental\",\"volume\":\"345 \",\"pages\":\"Article 123661\"},\"PeriodicalIF\":20.2000,\"publicationDate\":\"2023-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Catalysis B: Environmental\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0926337323013048\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environmental","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926337323013048","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
将联氨电氧化与氢进化反应（HER）耦合在一起用于生产节能型 H2 越来越受到关注。然而，肼辅助氢进化反应单元的性能受到了双功能催化剂未完全活化位点的限制。本文提出了一种表面局部重构策略，将无定形 Co(OH)2 和 P 空位 CoP 整合到 CoH-CoPV@CFP 催化剂中。Co(OH)2 中固有的缺电子 Co 位点具有很强的 N-Co 相互作用，可加速 N2H4 脱氢动力学，而 CoP 中形成的 P 空位则在缓和 H* 吸附能方面发挥了关键作用，从而获得了优异的双功能性。具体来说，在 10 mA cm-2 的条件下，它在碱性介质中对 HER 和 HzOR 的过电位分别为 -77 mV 和 -61 mV。实验室规模的电解槽可以在 0.23 V 的超低电池电压下提供 500 mA cm-2 的工业级电流密度。这种局部重构策略可能为设计肼辅助 H2 生成的高效催化剂铺平了新的道路。
Local-reconstruction enables cobalt phosphide array with bifunctional hydrogen evolution and hydrazine oxidation
Coupling hydrazine electrooxidation with hydrogen evolution reaction (HER) attracts ever-growing attention for energy-saving H2 production. However, the performance of hydrazine-assisted HER unit is restricted by the bifunctional catalysts with un-fully activated sites. Herein, a surface local-reconstruction strategy is proposed to integrate amorphous Co(OH)2 and P vacant CoP into the CoH-CoPV@CFP catalyst. The inherent electron-deficient Co sites in Co(OH)2 show strong N-Co interaction to accelerate the N2H4 dehydrogenation kinetics, while the as-formed P vacancies in CoP play a crucial role in moderating the H* adsorption energy, the excellent bifunctionality thus being obtained. Specifically, it achieves the low overpotentials of − 77 and − 61 mV at 10 mA cm−2 for HER and HzOR in alkaline media, respectively. A lab-scale electrolyzer can deliver the industrial-grade current density of 500 mA cm−2 under ultralow cell voltage of 0.23 V. This local-reconstruction strategy may pave new avenue to design efficient catalysts for hydrazine-assisted H2 generation.
期刊介绍：
Applied Catalysis B: Environment and Energy (formerly Applied Catalysis B: Environmental) is a journal that focuses on the transition towards cleaner and more sustainable energy sources. The journal's publications cover a wide range of topics, including:
1.Catalytic elimination of environmental pollutants such as nitrogen oxides, carbon monoxide, sulfur compounds, chlorinated and other organic compounds, and soot emitted from stationary or mobile sources.
2.Basic understanding of catalysts used in environmental pollution abatement, particularly in industrial processes.
3.All aspects of preparation, characterization, activation, deactivation, and regeneration of novel and commercially applicable environmental catalysts.
4.New catalytic routes and processes for the production of clean energy, such as hydrogen generation via catalytic fuel processing, and new catalysts and electrocatalysts for fuel cells.
5.Catalytic reactions that convert wastes into useful products.
6.Clean manufacturing techniques that replace toxic chemicals with environmentally friendly catalysts.
7.Scientific aspects of photocatalytic processes and a basic understanding of photocatalysts as applied to environmental problems.
8.New catalytic combustion technologies and catalysts.
9.New catalytic non-enzymatic transformations of biomass components.
The journal is abstracted and indexed in API Abstracts, Research Alert, Chemical Abstracts, Web of Science, Theoretical Chemical Engineering Abstracts, Engineering, Technology & Applied Sciences, and others.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
