• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

机械增强 NbC 纳米复合材料电极对析氢反应的高电催化响应。

High Electrocatalytic Response of a Mechanically Enhanced NbC Nanocomposite Electrode Toward Hydrogen Evolution Reaction.

机构信息

NanoBioMedical Centre, Adam Mickiewicz University , 85 Umultowska Str., 61614 Poznan, Poland.

CIC biomaGUNE , Paseo Miramón 182, 20009 San Sebastián, Spain.

出版信息

ACS Appl Mater Interfaces. 2017 Sep 13;9(36):30872-30879. doi: 10.1021/acsami.7b10317. Epub 2017 Sep 1.

DOI:10.1021/acsami.7b10317
PMID:28829574
Abstract

Resistant and efficient electrocatalysts for hydrogen evolution reaction (HER) are desired to replace scarce and commercially expensive platinum electrodes. Thin-film electrodes of metal carbides are a promising alternative due to their reduced price and similar catalytic properties. However, most of the studied structures neglect long-lasting chemical and structural stability, focusing only on electrochemical efficiency. Herein we report on a new approach to easily deposit and control the micro/nanostructure of thin-film electrodes based on niobium carbide (NbC) and their electrocatalytic response. We will show that, by improving the mechanical properties of the NbC electrodes, microstructure and mechanical resilience can be obtained while maintaining high electrocatalytic response. We also address the influence of other parameters such as conductivity and chemical composition on the overall performance of the thin-film electrodes. Finally, we show that nanocomposite NbC electrodes are promising candidates toward HER and, furthermore, that the methodology presented here is suitable to produce other transition-metal carbides with improved catalytic and mechanical properties.

摘要

为了替代稀缺且昂贵的铂电极,人们希望得到用于析氢反应(HER)的高效、耐蚀电催化剂。由于价格低廉且催化性能相似,金属碳化物薄膜电极是一种很有前途的替代品。然而,大多数研究结构都忽略了长期的化学和结构稳定性,仅关注电化学效率。在此,我们报告了一种新方法,该方法可以基于碳化铌(NbC)轻松沉积和控制薄膜电极的微/纳米结构及其电催化响应。我们将证明,通过提高 NbC 电极的机械性能,可以获得微结构和机械弹性,同时保持高电催化响应。我们还研究了其他参数(如导电性和化学成分)对薄膜电极整体性能的影响。最后,我们表明纳米复合 NbC 电极是析氢反应的有前途的候选材料,此外,本文提出的方法适用于制备具有改进的催化和机械性能的其他过渡金属碳化物。

相似文献

1
High Electrocatalytic Response of a Mechanically Enhanced NbC Nanocomposite Electrode Toward Hydrogen Evolution Reaction.机械增强 NbC 纳米复合材料电极对析氢反应的高电催化响应。
ACS Appl Mater Interfaces. 2017 Sep 13;9(36):30872-30879. doi: 10.1021/acsami.7b10317. Epub 2017 Sep 1.
2
Molybdenum Carbide-Based Electrocatalysts for Hydrogen Evolution Reaction.用于析氢反应的碳化钼基电催化剂
Chemistry. 2017 Aug 16;23(46):10947-10961. doi: 10.1002/chem.201701064. Epub 2017 Jul 4.
3
Self-Supported Transition-Metal-Based Electrocatalysts for Hydrogen and Oxygen Evolution.自支撑过渡金属基电催化剂用于析氢和析氧反应。
Adv Mater. 2020 Jan;32(3):e1806326. doi: 10.1002/adma.201806326. Epub 2019 Apr 1.
4
General Strategy for the Synthesis of Transition Metal Phosphide Films for Electrocatalytic Hydrogen and Oxygen Evolution.用于电催化析氢和析氧的过渡金属磷化物薄膜的合成通用策略。
ACS Appl Mater Interfaces. 2016 May 25;8(20):12798-803. doi: 10.1021/acsami.6b02352. Epub 2016 May 16.
5
Self-Supported Biocarbon-Fiber Electrode Decorated with Molybdenum Carbide Nanoparticles for Highly Active Hydrogen-Evolution Reaction.自支撑生物碳纤维电极负载碳化钼纳米粒子用于高效析氢反应。
ACS Appl Mater Interfaces. 2017 Jul 12;9(27):22604-22611. doi: 10.1021/acsami.7b06075. Epub 2017 Jun 28.
6
Structural Design and Electronic Modulation of Transition-Metal-Carbide Electrocatalysts toward Efficient Hydrogen Evolution.过渡金属碳化物电催化剂的结构设计与电子调控实现高效析氢。
Adv Mater. 2019 Jan;31(2):e1802880. doi: 10.1002/adma.201802880. Epub 2018 Aug 21.
7
Multidimensional Thin Film Hybrid Electrodes with MoS Multilayer for Electrocatalytic Hydrogen Evolution Reaction.用于电催化析氢反应的 MoS 多层的多维薄膜混合电极。
ACS Appl Mater Interfaces. 2017 Mar 15;9(10):8688-8695. doi: 10.1021/acsami.6b15251. Epub 2017 Mar 6.
8
A review of modulation strategies for improving the catalytic performance of transition metal sulfide self-supported electrodes for the hydrogen evolution reaction.用于提高过渡金属硫化物自支撑电极析氢反应催化性能的调制策略综述。
Dalton Trans. 2024 Feb 27;53(9):3959-3969. doi: 10.1039/d3dt04244h.
9
A new class of electrocatalysts for hydrogen production from water electrolysis: metal monolayers supported on low-cost transition metal carbides.一类用于水电解制氢的新型电催化剂:负载在低成本过渡金属碳化物上的金属单原子层。
J Am Chem Soc. 2012 Feb 15;134(6):3025-33. doi: 10.1021/ja208656v. Epub 2012 Feb 1.
10
Porous molybdenum carbide nano-octahedrons synthesized via confined carburization in metal-organic frameworks for efficient hydrogen production.通过在金属有机框架中进行受限渗碳合成的多孔碳化钼纳米八面体用于高效制氢。
Nat Commun. 2015 Mar 11;6:6512. doi: 10.1038/ncomms7512.

引用本文的文献

1
High sensitivity voltammetric sensor of 4-nitrotoluene based on nanoflake-rich boron-doped carbon nanowall electrode for water safety.基于富含纳米片的硼掺杂碳纳米壁电极的4-硝基甲苯高灵敏度伏安传感器用于水安全检测。
Mikrochim Acta. 2025 Mar 5;192(4):208. doi: 10.1007/s00604-025-07065-5.
2
Solid-State Synthesis of Niobium Carbide Electrocatalyst in the Presence of Vanadium as Suppressor of Energy Input and Greenhouse Gas Emission.在钒作为能量输入和温室气体排放抑制剂存在的情况下碳化铌电催化剂的固态合成
ACS Omega. 2024 Jan 31;9(6):7069-7074. doi: 10.1021/acsomega.3c09045. eCollection 2024 Feb 13.
3
Synthesis of niobium(iv) carbide nanoparticles an alkali-molten-method at a spatially-limited surface of mesoporous carbon.
在介孔碳的空间受限表面通过碱熔法合成碳化铌(IV)纳米颗粒。
RSC Adv. 2023 Aug 22;13(36):24918-24924. doi: 10.1039/d3ra03254j. eCollection 2023 Aug 21.
4
Investigation of polymer-derived Si-(B)-C-N ceramic/reduced graphene oxide composite systems as active catalysts towards the hydrogen evolution reaction.聚合物衍生的Si-(B)-C-N陶瓷/还原氧化石墨烯复合体系作为析氢反应活性催化剂的研究。
Sci Rep. 2020 Dec 15;10(1):22003. doi: 10.1038/s41598-020-78558-x.
5
Low temperature synthesis of NbC/C nano-composites as visible light photoactive catalyst.作为可见光光活性催化剂的NbC/C纳米复合材料的低温合成
Sci Rep. 2018 Sep 11;8(1):13597. doi: 10.1038/s41598-018-31989-z.