Engineered Interfaces of Nickel–Iron Nitride and Cobalt Oxide on Nitrogen-Doped Carbon Nanoribbons: A Catalytic High-Efficiency Zone for Water Splitting

IF 5.2 3区 工程技术 Q2 ENERGY & FUELS
Arooj Nisar, Arslan Hameed, Ghulam Mustafa, Guobao Xu* and Muhammad Arif Nadeem*, 
{"title":"Engineered Interfaces of Nickel–Iron Nitride and Cobalt Oxide on Nitrogen-Doped Carbon Nanoribbons: A Catalytic High-Efficiency Zone for Water Splitting","authors":"Arooj Nisar,&nbsp;Arslan Hameed,&nbsp;Ghulam Mustafa,&nbsp;Guobao Xu* and Muhammad Arif Nadeem*,&nbsp;","doi":"10.1021/acs.energyfuels.5c0089510.1021/acs.energyfuels.5c00895","DOIUrl":null,"url":null,"abstract":"<p >Electrocatalytic energy conversions are vital for advancing clean energy technologies, enabling processes such as water electrolysis that rely on electrochemical redox reactions at catalyst surfaces. Transition metal nitrides (TMNs) are considered as promising electrode materials due to their abundance, low cost, and noble metal-like electronic structure. In this work, we have synthesized nickel iron nitride supported over nitrogen-doped carbon nanoribbons designated as NiFeN@CoOx/N-CNRs via a facile two-step process. This involves the hydrothermal fabrication of NiFe-LDH on ZIF-12-derived CoOx/N-CNRs, followed by nitridation. The as-obtained composite NiFeN@CoOx/N-CNRs serves as a competent bifunctional electrode, delivering a current density of 20 mA/cm<sup>2</sup> at a sufficiently low overpotential (η) of 233 mV for the oxygen evolution reaction (OER) and 75 mV for hydrogen evolution reaction (HER). Moreover, it demonstrated fast reaction kinetics, minimal resistance to charge transfer (<i>R</i><sub>ct</sub>), a large electrochemically active surface area, and outstanding stability in alkaline reaction conditions for both OER and HER. These enhancements are attributed to the formation of a heterointerface between NiFeN and CoOx/N-CNRs, which facilitates superior charge migration and exploits the unique electronic properties of bimetallic nitrides. The hierarchical structure of the LDH precursor and the incorporation of N-CNRs further enhance conductivity, contributing to improved overall performance. This study provides a significant approach for fabricating and optimizing TMNs to be used as bifunctional electrodes in industrial alkaline water electrolyzers.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 21","pages":"9968–9980 9968–9980"},"PeriodicalIF":5.2000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00895","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

Electrocatalytic energy conversions are vital for advancing clean energy technologies, enabling processes such as water electrolysis that rely on electrochemical redox reactions at catalyst surfaces. Transition metal nitrides (TMNs) are considered as promising electrode materials due to their abundance, low cost, and noble metal-like electronic structure. In this work, we have synthesized nickel iron nitride supported over nitrogen-doped carbon nanoribbons designated as NiFeN@CoOx/N-CNRs via a facile two-step process. This involves the hydrothermal fabrication of NiFe-LDH on ZIF-12-derived CoOx/N-CNRs, followed by nitridation. The as-obtained composite NiFeN@CoOx/N-CNRs serves as a competent bifunctional electrode, delivering a current density of 20 mA/cm2 at a sufficiently low overpotential (η) of 233 mV for the oxygen evolution reaction (OER) and 75 mV for hydrogen evolution reaction (HER). Moreover, it demonstrated fast reaction kinetics, minimal resistance to charge transfer (Rct), a large electrochemically active surface area, and outstanding stability in alkaline reaction conditions for both OER and HER. These enhancements are attributed to the formation of a heterointerface between NiFeN and CoOx/N-CNRs, which facilitates superior charge migration and exploits the unique electronic properties of bimetallic nitrides. The hierarchical structure of the LDH precursor and the incorporation of N-CNRs further enhance conductivity, contributing to improved overall performance. This study provides a significant approach for fabricating and optimizing TMNs to be used as bifunctional electrodes in industrial alkaline water electrolyzers.

氮掺杂碳纳米带上氮化镍铁和氧化钴的工程界面:水裂解的催化高效区
电催化能量转换对于推进清洁能源技术至关重要,使水电解等依赖于催化剂表面电化学氧化还原反应的过程成为可能。过渡金属氮化物(TMNs)因其丰富、低成本和贵金属样电子结构而被认为是一种很有前途的电极材料。在这项工作中,我们通过简单的两步法合成了氮掺杂碳纳米带(指定为NiFeN@CoOx/N-CNRs)上的氮化镍铁。这涉及到在zif -12衍生的CoOx/N-CNRs上水热制备NiFe-LDH,然后进行氮化。所获得的复合材料NiFeN@CoOx/N-CNRs可作为双功能电极,在足够低的过电位(η)为233 mV时提供20 mA/cm2的电流密度,用于析氧反应(OER)和75 mV的析氢反应(HER)。此外,它还表现出快速的反应动力学,最小的电荷转移阻力(Rct),大的电化学活性表面积,以及在碱性反应条件下OER和HER的出色稳定性。这些增强归因于NiFeN和CoOx/ n - cnr之间形成的异质界面,这有利于优越的电荷迁移,并利用了双金属氮化物独特的电子特性。LDH前驱体的分层结构和n - cnr的掺入进一步提高了电导率,有助于提高整体性能。本研究为制备和优化用于工业碱性水电解槽双功能电极的TMNs提供了重要途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
期刊介绍: Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信