Jae Won Choi, Ayeong Byeon, Sooyeon Kim, Chang-Kyu Hwang, Wenjun Zhang, Jimin Lee, Won Chan Yun, Sae Yane Paek, Jin Hyeung Kim, Giho Jeong, Seung Yong Lee, Joonhee Moon, Sang Soo Han, Jae W. Lee, Jong Min Kim
{"title":"Mesoporous Boron-Doped Carbon with Curved B4C Active Sites for Highly Efficient H2O2 Electrosynthesis in Neutral Media and Air-Supplied Environments","authors":"Jae Won Choi, Ayeong Byeon, Sooyeon Kim, Chang-Kyu Hwang, Wenjun Zhang, Jimin Lee, Won Chan Yun, Sae Yane Paek, Jin Hyeung Kim, Giho Jeong, Seung Yong Lee, Joonhee Moon, Sang Soo Han, Jae W. Lee, Jong Min Kim","doi":"10.1002/adma.202415712","DOIUrl":null,"url":null,"abstract":"Hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) electrosynthesis via the 2e<sup>−</sup> oxygen reduction reaction (ORR) is considered as a cost-effective and safe alternative to the energy-intensive anthraquinone process. However, in more practical environments, namely, the use of neutral media and air-fed cathode environments, slow ORR kinetics and insufficient oxygen supply pose significant challenges to efficient H<sub>2</sub>O<sub>2</sub> production at high current densities. In this work, mesoporous B-doped carbons with novel curved B<sub>4</sub>C active sites, synthesized via a carbon dioxide (CO<sub>2</sub>) reduction using a pore-former agent, to simultaneously achieve excellent 2e<sup>−</sup> ORR activity and improved mass transfer properties are introduced. Through a combination of experimental analysis and theoretical calculations, it is confirmed that the curved B<sub>4</sub>C configuration, formed by mesopores in the carbon, demonstrates superior selectivity and activity for 2e<sup>−</sup> ORR due to its weaker interaction with *OOH intermediates compared to planar B<sub>4</sub>C in neutral media. Moreover, the mesopores facilitate oxygen supply and suppress the hydrogen evolution reaction, achieving a Faradaic efficiency of 86.2% at 150 mA cm<sup>−2</sup> under air-supplied conditions, along with an impressive O<sub>2</sub> utilization efficiency of 93.6%. This approach will provide a route to catalyst design for efficient H<sub>2</sub>O<sub>2</sub> electrosynthesis in a practical environment.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"26 1","pages":""},"PeriodicalIF":27.4000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202415712","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrogen peroxide (H2O2) electrosynthesis via the 2e− oxygen reduction reaction (ORR) is considered as a cost-effective and safe alternative to the energy-intensive anthraquinone process. However, in more practical environments, namely, the use of neutral media and air-fed cathode environments, slow ORR kinetics and insufficient oxygen supply pose significant challenges to efficient H2O2 production at high current densities. In this work, mesoporous B-doped carbons with novel curved B4C active sites, synthesized via a carbon dioxide (CO2) reduction using a pore-former agent, to simultaneously achieve excellent 2e− ORR activity and improved mass transfer properties are introduced. Through a combination of experimental analysis and theoretical calculations, it is confirmed that the curved B4C configuration, formed by mesopores in the carbon, demonstrates superior selectivity and activity for 2e− ORR due to its weaker interaction with *OOH intermediates compared to planar B4C in neutral media. Moreover, the mesopores facilitate oxygen supply and suppress the hydrogen evolution reaction, achieving a Faradaic efficiency of 86.2% at 150 mA cm−2 under air-supplied conditions, along with an impressive O2 utilization efficiency of 93.6%. This approach will provide a route to catalyst design for efficient H2O2 electrosynthesis in a practical environment.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.