{"title":"多角度设计空心结构铈钒基纳米柱阵列,增强整体水电解能力。","authors":"Yan Qin, Caizheng Wang, Xinran Hou, Huijie Zhang, Zhaoyang Tan, Xiaobin Wang, Jingde Li, Feichao Wu","doi":"10.1016/j.jcis.2024.07.104","DOIUrl":null,"url":null,"abstract":"<p><p>It is critical and challenging to develop highly active and low cost bifunctional electrocatalysts for the hydrogen/oxygen evolution reaction (HER/OER) in water electrolysis. Herein, we propose cerium-vanadium-based hollow nanopillar arrays supported on nickel foam (CeV-HNA/NF) as bifunctional HER/OER electrocatalysts, which are prepared by etching the V metal-organic framework with Ce salt and then pyrolyzing. Etching results in multidimensional optimizations of electrocatalysts, covering substantial oxygen vacancies, optimized electronic configurations, and an open-type structure of hollow nanopillar arrays, which contribute to accelerating the charge transfer rate, regulating the adsorption energy of H/O-containing reaction intermediates, and fully exposing the active sites. The reconstruction of the electrocatalyst is also accelerated by Ce doping, which results in highly active hydroxy vanadium oxide interfaces. Therefore, extremely low overpotentials of 170 and 240 mV under a current density of 100 mA cm<sup>-2</sup> are achieved for the HER and OER under alkaline conditions, respectively, with long-term stability for 300 h. An electrolysis cell with CeV-HNA/NF as both the cathode and anode delivers a small voltage of 1.53 V to achieve water electrolysis under 10 mA cm<sup>-2</sup>, accompanied by superior durability for 150 h. This design provides an innovative way to develop advanced bifunctional electrocatalysts for overall water electrolysis.</p>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"674 ","pages":"1092-1102"},"PeriodicalIF":9.4000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiple-perspective design of hollow-structured cerium-vanadium-based nanopillar arrays for enhanced overall water electrolysis.\",\"authors\":\"Yan Qin, Caizheng Wang, Xinran Hou, Huijie Zhang, Zhaoyang Tan, Xiaobin Wang, Jingde Li, Feichao Wu\",\"doi\":\"10.1016/j.jcis.2024.07.104\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>It is critical and challenging to develop highly active and low cost bifunctional electrocatalysts for the hydrogen/oxygen evolution reaction (HER/OER) in water electrolysis. Herein, we propose cerium-vanadium-based hollow nanopillar arrays supported on nickel foam (CeV-HNA/NF) as bifunctional HER/OER electrocatalysts, which are prepared by etching the V metal-organic framework with Ce salt and then pyrolyzing. Etching results in multidimensional optimizations of electrocatalysts, covering substantial oxygen vacancies, optimized electronic configurations, and an open-type structure of hollow nanopillar arrays, which contribute to accelerating the charge transfer rate, regulating the adsorption energy of H/O-containing reaction intermediates, and fully exposing the active sites. The reconstruction of the electrocatalyst is also accelerated by Ce doping, which results in highly active hydroxy vanadium oxide interfaces. Therefore, extremely low overpotentials of 170 and 240 mV under a current density of 100 mA cm<sup>-2</sup> are achieved for the HER and OER under alkaline conditions, respectively, with long-term stability for 300 h. An electrolysis cell with CeV-HNA/NF as both the cathode and anode delivers a small voltage of 1.53 V to achieve water electrolysis under 10 mA cm<sup>-2</sup>, accompanied by superior durability for 150 h. 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引用次数: 0
摘要
为电解水中的氢/氧进化反应(HER/OER)开发高活性、低成本的双功能电催化剂既重要又具有挑战性。在此,我们提出以铈钒为基础、以泡沫镍为支撑的中空纳米柱阵列(CeV-HNA/NF)作为双功能 HER/OER 电催化剂,其制备方法是用铈盐蚀刻 V 金属有机框架,然后进行热解。蚀刻工艺可对电催化剂进行多维优化,包括大量的氧空位、优化的电子构型以及中空纳米柱阵列的开放型结构,这些都有助于加快电荷转移速率、调节含 H/O 反应中间产物的吸附能以及充分暴露活性位点。掺杂 Ce 还能加速电催化剂的重构,从而形成高活性的羟基氧化钒界面。因此,在 100 mA cm-2 的电流密度下,碱性条件下的 HER 和 OER 可分别达到 170 mV 和 240 mV 的极低过电位,并可长期稳定运行 300 小时;同时使用 CeV-HNA/NF 作为阴极和阳极的电解池可在 10 mA cm-2 的电流密度下提供 1.53 V 的小电压实现水电解,并可在 150 小时内保持卓越的耐久性。
Multiple-perspective design of hollow-structured cerium-vanadium-based nanopillar arrays for enhanced overall water electrolysis.
It is critical and challenging to develop highly active and low cost bifunctional electrocatalysts for the hydrogen/oxygen evolution reaction (HER/OER) in water electrolysis. Herein, we propose cerium-vanadium-based hollow nanopillar arrays supported on nickel foam (CeV-HNA/NF) as bifunctional HER/OER electrocatalysts, which are prepared by etching the V metal-organic framework with Ce salt and then pyrolyzing. Etching results in multidimensional optimizations of electrocatalysts, covering substantial oxygen vacancies, optimized electronic configurations, and an open-type structure of hollow nanopillar arrays, which contribute to accelerating the charge transfer rate, regulating the adsorption energy of H/O-containing reaction intermediates, and fully exposing the active sites. The reconstruction of the electrocatalyst is also accelerated by Ce doping, which results in highly active hydroxy vanadium oxide interfaces. Therefore, extremely low overpotentials of 170 and 240 mV under a current density of 100 mA cm-2 are achieved for the HER and OER under alkaline conditions, respectively, with long-term stability for 300 h. An electrolysis cell with CeV-HNA/NF as both the cathode and anode delivers a small voltage of 1.53 V to achieve water electrolysis under 10 mA cm-2, accompanied by superior durability for 150 h. This design provides an innovative way to develop advanced bifunctional electrocatalysts for overall water electrolysis.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies