{"title":"Hyper-Cross-Linked Polymer-Derived Carbon-Coated Fe–Ni Alloy/CNT as a Bifunctional Electrocatalyst for Rechargeable Zinc–Air Batteries","authors":"Arindam Modak, Ankita Phutela, Aniruddha Kundu, Srijib Das, Vidha Bhasin, Dibyendu Bhattacharyya, Saswata Bhattacharya","doi":"10.1021/acs.jpclett.4c03361","DOIUrl":null,"url":null,"abstract":"The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are considered to be the most important processes in metal–air batteries and regenerative fuel cell devices. Metal–organic polymers are attracting interest as promising precursors of advanced metal/carbon electrocatalysts because of their hierarchical porous structure along with the integrated metal–carbon framework. We developed carbon-coated CNTs with Ni/Fe and Cu/Fe as active sites. Experimental observations from X-ray photoelectron spectroscopy and X-ray absorption analysis suggest that C@CNT[Ni] outperforms C@CNT[Cu] in the ORR and OER, which is further supported by density functional theory calculations. C@CNT[Ni] exhibits a higher onset potential (0.99 V vs RHE) and a smaller Tafel slope (40.2 mV decade<sup>–1</sup>) compared to those of C@CNT/[Cu] in an alkaline electrolyte (0.94 V vs RHE and 46.5 mV decade<sup>–1</sup>, respectively). Such circumstances are attributed to the alloying effect between Ni and Fe in C@CNT[Ni], in contrast to the existing copper iron oxide phase in C@CNT/[Cu]. It is noteworthy that C@CNT[Ni] also displayed an improved OER, demanding its bifunctional property. As a proof of concept, C@CNT[Ni] was utilized in zinc–air batteries, which shows a high energy efficiency of ∼60%, a small charge–discharge voltage gap of 0.78 V, and excellent cycling performance (∼120 h) at 5 mA cm<sup>–2</sup> and 25 °C. This protocol expands the utility of novel metal–organic hyper-cross-linked polymer-derived bimetallic electrocatalysts for clean energy research.","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"59 1","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpclett.4c03361","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are considered to be the most important processes in metal–air batteries and regenerative fuel cell devices. Metal–organic polymers are attracting interest as promising precursors of advanced metal/carbon electrocatalysts because of their hierarchical porous structure along with the integrated metal–carbon framework. We developed carbon-coated CNTs with Ni/Fe and Cu/Fe as active sites. Experimental observations from X-ray photoelectron spectroscopy and X-ray absorption analysis suggest that C@CNT[Ni] outperforms C@CNT[Cu] in the ORR and OER, which is further supported by density functional theory calculations. C@CNT[Ni] exhibits a higher onset potential (0.99 V vs RHE) and a smaller Tafel slope (40.2 mV decade–1) compared to those of C@CNT/[Cu] in an alkaline electrolyte (0.94 V vs RHE and 46.5 mV decade–1, respectively). Such circumstances are attributed to the alloying effect between Ni and Fe in C@CNT[Ni], in contrast to the existing copper iron oxide phase in C@CNT/[Cu]. It is noteworthy that C@CNT[Ni] also displayed an improved OER, demanding its bifunctional property. As a proof of concept, C@CNT[Ni] was utilized in zinc–air batteries, which shows a high energy efficiency of ∼60%, a small charge–discharge voltage gap of 0.78 V, and excellent cycling performance (∼120 h) at 5 mA cm–2 and 25 °C. This protocol expands the utility of novel metal–organic hyper-cross-linked polymer-derived bimetallic electrocatalysts for clean energy research.
氧还原反应(ORR)和析氧反应(OER)被认为是金属空气电池和再生燃料电池装置中最重要的过程。金属-有机聚合物由于其层叠多孔结构和金属-碳一体化框架而成为先进金属/碳电催化剂的前驱体。我们开发了以Ni/Fe和Cu/Fe作为活性位点的碳包覆CNTs。x射线光电子能谱和x射线吸收分析的实验观测结果表明,C@CNT[Ni]在ORR和OER中优于C@CNT[Cu],密度泛函理论计算进一步支持了这一结论。与C@CNT/[Cu]相比,C@CNT[Ni]在碱性电解质中表现出更高的起始电位(0.99 V vs RHE)和更小的Tafel斜率(40.2 mV decade-1)(分别为0.94 V vs RHE和46.5 mV decade-1)。这种情况归因于C@CNT[Ni]中Ni和Fe之间的合金化作用,而C@CNT/[Cu]中存在铜氧化铁相。值得注意的是,C@CNT[Ni]也显示出改进的OER,要求其双功能特性。作为概念验证,C@CNT[Ni]被用于锌空气电池中,该电池显示出高达60%的高能量效率,0.78 V的小充放电电压间隙,以及在5 mA cm-2和25°C下优异的循环性能(~ 120 h)。该协议扩大了新型金属-有机超交联聚合物衍生双金属电催化剂在清洁能源研究中的应用。
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.