Chunsheng Ding, Qiwen Su, Xiaowen Ruan, Dongxu Jiao, Hao Cai, Minghua Xu, Wei Zhang, Hongwei Huang, Sai Kishore Ravi, Xiaoqiang Cui
{"title":"Polydopamine‐Modified BiOX with Interfacial p‐Orbital Coupling Enhances Superoxide Conversion for Efficient Piezocatalytic H2O2 Production","authors":"Chunsheng Ding, Qiwen Su, Xiaowen Ruan, Dongxu Jiao, Hao Cai, Minghua Xu, Wei Zhang, Hongwei Huang, Sai Kishore Ravi, Xiaoqiang Cui","doi":"10.1002/aenm.202503493","DOIUrl":null,"url":null,"abstract":"Hydrogen peroxide (H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>) production via piezocatalysis offers a sustainable route to convert mechanical energy into chemical oxidants using water and oxygen. However, its efficiency is limited by sluggish surface redox kinetics, particularly the conversion of key radical intermediates (•O<jats:sub>2</jats:sub><jats:sup>−</jats:sup> and •OH), and by the kinetic mismatch between charge carrier transfer and proton availability. Here, a polydopamine‐modified bismuth oxide halide (BiOX, X = Cl, Br, I) catalyst is reported that achieves a high piezocatalytic H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> production rate of 3083 µmol g<jats:sup>−1</jats:sup> h<jats:sup>−1</jats:sup> and maintains stable activity across a broad pH range (3–9). Spectroscopic analyses and density functional theory calculations reveal that the polydopamine layer introduces interfacial p‐orbital interactions between carbon (from polydopamine) and bismuth sites, which enhance O<jats:sub>2</jats:sub> adsorption, lower the energy barrier for •O<jats:sub>2</jats:sub><jats:sup>−</jats:sup> to •OOH conversion, and accelerate water oxidation for proton supply. This synergistic modulation of radical reaction pathways enables efficient and selective H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> generation. The as‐produced H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> demonstrates practical utility in pollutant degradation and antimicrobial applications. These findings establish a rational strategy for designing piezocatalysts by engineering interfacial orbital coupling to control reaction intermediate dynamics.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"102 1","pages":""},"PeriodicalIF":26.0000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202503493","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrogen peroxide (H2O2) production via piezocatalysis offers a sustainable route to convert mechanical energy into chemical oxidants using water and oxygen. However, its efficiency is limited by sluggish surface redox kinetics, particularly the conversion of key radical intermediates (•O2− and •OH), and by the kinetic mismatch between charge carrier transfer and proton availability. Here, a polydopamine‐modified bismuth oxide halide (BiOX, X = Cl, Br, I) catalyst is reported that achieves a high piezocatalytic H2O2 production rate of 3083 µmol g−1 h−1 and maintains stable activity across a broad pH range (3–9). Spectroscopic analyses and density functional theory calculations reveal that the polydopamine layer introduces interfacial p‐orbital interactions between carbon (from polydopamine) and bismuth sites, which enhance O2 adsorption, lower the energy barrier for •O2− to •OOH conversion, and accelerate water oxidation for proton supply. This synergistic modulation of radical reaction pathways enables efficient and selective H2O2 generation. The as‐produced H2O2 demonstrates practical utility in pollutant degradation and antimicrobial applications. These findings establish a rational strategy for designing piezocatalysts by engineering interfacial orbital coupling to control reaction intermediate dynamics.
期刊介绍:
Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small.
With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics.
The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.