{"title":"Synergistically enhanced ORR and HER performance on Co-N-C coupled in-situ generated PtCo intermetallic","authors":"","doi":"10.1016/j.jechem.2024.09.023","DOIUrl":null,"url":null,"abstract":"<div><div>Integrating multi-scale sites in a composite catalyst is vital to realize efficient electrocatalysis. Herein, a synergistic composite catalyst consisting of Co atomic sites and in-situ generated PtCo intermetallic compounds (IMCs) (<em>o</em>-PtCo@CoNC) is proposed through Co pre-anchoring and subsequent impregnation-reduction method. High loading of Co atoms provides a chance for in-situ generating PtCo ordered intermetallic compounds. The remaining Co single atoms and PtCo IMCs construct synergistic electrocatalytic micro-regions. Benefiting from the ordered structure, synergistic effect of PtCo IMCs and Co single atoms, <em>o</em>-PtCo@CoNC exhibits excellent electrocatalytic performance for oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) with mass activity of 1.21 A mg<sub>Pt</sub><sup>−1</sup> (at 0.9 V) and 5.70 A mg<sub>Pt</sub><sup>−1</sup> (at an overpotential of 100 mV), respectively. Besides, <em>o</em>-PtCo@CoNC delivers negligible loss of half-wave potential and overpotential during long-term stability test in acid solutions, with 13 mV decay after 50,000 potential cycles for ORR and a 2.7 mV decay after 20,000 potential cycles for HER. The integration strategy of single-atomic sites coupled IMCs paves the way for enhancing the activity and durability of Pt-based electrocatalysts.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":null,"pages":null},"PeriodicalIF":13.1000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495624006466","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0
Abstract
Integrating multi-scale sites in a composite catalyst is vital to realize efficient electrocatalysis. Herein, a synergistic composite catalyst consisting of Co atomic sites and in-situ generated PtCo intermetallic compounds (IMCs) (o-PtCo@CoNC) is proposed through Co pre-anchoring and subsequent impregnation-reduction method. High loading of Co atoms provides a chance for in-situ generating PtCo ordered intermetallic compounds. The remaining Co single atoms and PtCo IMCs construct synergistic electrocatalytic micro-regions. Benefiting from the ordered structure, synergistic effect of PtCo IMCs and Co single atoms, o-PtCo@CoNC exhibits excellent electrocatalytic performance for oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) with mass activity of 1.21 A mgPt−1 (at 0.9 V) and 5.70 A mgPt−1 (at an overpotential of 100 mV), respectively. Besides, o-PtCo@CoNC delivers negligible loss of half-wave potential and overpotential during long-term stability test in acid solutions, with 13 mV decay after 50,000 potential cycles for ORR and a 2.7 mV decay after 20,000 potential cycles for HER. The integration strategy of single-atomic sites coupled IMCs paves the way for enhancing the activity and durability of Pt-based electrocatalysts.
在复合催化剂中整合多尺度位点对于实现高效电催化至关重要。本文通过 Co 预锚定和随后的浸渍还原方法,提出了一种由 Co 原子位点和原位生成的铂钴金属间化合物(IMCs)(o-PtCo@CoNC)组成的协同复合催化剂。高含量的 Co 原子为原位生成铂钴有序金属间化合物提供了机会。剩余的 Co 单原子和 PtCo IMC 构建了协同电催化微区。得益于有序结构、PtCo IMCs 和 Co 单原子的协同效应,o-PtCo@CoNC 在氧还原反应(ORR)和氢进化反应(HER)中表现出优异的电催化性能,质量活性分别为 1.21 A mgPt-1(0.9 V 时)和 5.70 A mgPt-1(100 mV 过电位时)。此外,在酸溶液中进行长期稳定性测试时,o-PtCo@CoNC 的半波电位和过电位损失微乎其微,ORR 在 50,000 次电位循环后衰减 13 mV,HER 在 20,000 次电位循环后衰减 2.7 mV。单原子位点耦合 IMC 的集成策略为提高铂基电催化剂的活性和耐用性铺平了道路。
期刊介绍:
The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
This journal focuses on original research papers covering various topics within energy chemistry worldwide, including:
Optimized utilization of fossil energy
Hydrogen energy
Conversion and storage of electrochemical energy
Capture, storage, and chemical conversion of carbon dioxide
Materials and nanotechnologies for energy conversion and storage
Chemistry in biomass conversion
Chemistry in the utilization of solar energy