{"title":"Balancing the Aggregation of Cobalt Phthalocyanine on Carbon Nanohorn for Efficient H2O2 electrosynthesis in Neutral Electrolyte","authors":"Yiqi Ding, Zhuo Xing, Chunguang Kuai, Feng Ryan Wang, Yuzheng Guo","doi":"10.1002/celc.202400650","DOIUrl":null,"url":null,"abstract":"<p>Oxygen reduction reaction (ORR) driven by renewable electricity in neutral electrolyte presents a promising way for generating H<sub>2</sub>O<sub>2</sub>, which is suitable for daily sanitation and hygiene management. Cobalt phthalocyanine (CoPc) serves as an effective molecular electrocatalyst, providing active sites to facilitate H<sub>2</sub>O<sub>2</sub> generation during ORR through a uniform distribution on carbon supports. However, the catalytic performance currently falls short of industrial application requirements. Herein, we employed carbon nanohorns with abundant oxygen functional groups (CNH(O)) to support CoPc, thereby optimizing the distribution of CoPc and enhancing the generation of active sites with electron-deficient Co centres. Control experiments and characterizations demonstrate the electron-deficient of Co centres is dependent on the degree of CoPc aggregation, highlighting a trade-off between loading weight and distribution of CoPc. Then, a 4% loading weight of CoPc on CNH(O) exhibited the optimal performance of H<sub>2</sub>O<sub>2</sub> generation, achieving a H<sub>2</sub>O<sub>2</sub> current density of 483 mA cm<sup>−2</sup> at a potential of 0.3 V vs RHE with a Faradaic efficiency of 64 %.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 9","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400650","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemElectroChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/celc.202400650","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Oxygen reduction reaction (ORR) driven by renewable electricity in neutral electrolyte presents a promising way for generating H2O2, which is suitable for daily sanitation and hygiene management. Cobalt phthalocyanine (CoPc) serves as an effective molecular electrocatalyst, providing active sites to facilitate H2O2 generation during ORR through a uniform distribution on carbon supports. However, the catalytic performance currently falls short of industrial application requirements. Herein, we employed carbon nanohorns with abundant oxygen functional groups (CNH(O)) to support CoPc, thereby optimizing the distribution of CoPc and enhancing the generation of active sites with electron-deficient Co centres. Control experiments and characterizations demonstrate the electron-deficient of Co centres is dependent on the degree of CoPc aggregation, highlighting a trade-off between loading weight and distribution of CoPc. Then, a 4% loading weight of CoPc on CNH(O) exhibited the optimal performance of H2O2 generation, achieving a H2O2 current density of 483 mA cm−2 at a potential of 0.3 V vs RHE with a Faradaic efficiency of 64 %.
由可再生电力驱动的氧还原反应(ORR)在中性电解质中生成H2O2是一种很有前途的方法,适用于日常卫生和卫生管理。酞菁钴(CoPc)作为一种有效的分子电催化剂,通过在碳载体上的均匀分布,在ORR过程中提供促进H2O2生成的活性位点。但目前其催化性能还达不到工业应用要求。本研究中,我们使用了含有丰富氧官能团(CNH(O))的碳纳米角来支持CoPc,从而优化了CoPc的分布,并增强了缺乏电子的Co中心活性位点的产生。对照实验和表征表明,Co中心的缺电子依赖于CoPc的聚集程度,强调了负载重量和CoPc分布之间的权衡。然后,在CNH(O)上负载4%的CoPc表现出最佳的H2O2生成性能,在0.3 V vs RHE电位下,H2O2电流密度为483 mA cm−2,法拉第效率为64%。
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.