Shichu Zhao , Yuping Du , Hang Zhang , Minzhi Ma , Jiawei Zhang , Mengge Jia , Weiwei He , Zhi Zheng , Wenjun Fa
{"title":"通过在MnOx/WO3上诱导孔积累提高微量H2O2的光电化学检测精度","authors":"Shichu Zhao , Yuping Du , Hang Zhang , Minzhi Ma , Jiawei Zhang , Mengge Jia , Weiwei He , Zhi Zheng , Wenjun Fa","doi":"10.1016/j.jelechem.2025.119254","DOIUrl":null,"url":null,"abstract":"<div><div>Restrained by sluggish migration dynamics of holes, the detection sensitivity and limit of an anodic photoelectrochemical (APEC) strategy for trace hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) is generally difficult to meet the demands of the current chemical industry. Herein, interface hole enrichment engineering is proposed to solve this challenge. Subsequently, manganese oxide species (MnO<sub>x</sub>) was photo-deposited on tungsten trioxide (WO<sub>3</sub>) as a proof-of-concept prototype photoanode. Photoelectric structure characterization demonstrated that MnO<sub>x</sub> species were validated to diminish H<sub>2</sub>O<sub>2</sub> oxidation overpotential by increasing the concentration and lifetime of photogenerated holes, accelerating significantly H<sub>2</sub>O<sub>2</sub> oxidation. As a result, the MnO<sub>x</sub>/WO<sub>3</sub> photoanode achieves a lower detection limit of 0.1 mM and a higher sensitivity of 4.81 μA cm<sup>−2</sup> mM<sup>−1</sup> for H<sub>2</sub>O<sub>2</sub> detection respectively, which are 0.125 (0.8 mM) and 1.72 (2.79 μA cm<sup>−2</sup> mM<sup>−1</sup>) times sensitive compared to that of WO<sub>3</sub> photoanode. This work demonstrates a hole enrichment strategy to boost the sensitivity of trace H<sub>2</sub>O<sub>2</sub> analysis.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"993 ","pages":"Article 119254"},"PeriodicalIF":4.1000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosting photoelectrochemical detection accuracy of trace H2O2 by inducing holes accumulation on the MnOx/WO3\",\"authors\":\"Shichu Zhao , Yuping Du , Hang Zhang , Minzhi Ma , Jiawei Zhang , Mengge Jia , Weiwei He , Zhi Zheng , Wenjun Fa\",\"doi\":\"10.1016/j.jelechem.2025.119254\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Restrained by sluggish migration dynamics of holes, the detection sensitivity and limit of an anodic photoelectrochemical (APEC) strategy for trace hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) is generally difficult to meet the demands of the current chemical industry. Herein, interface hole enrichment engineering is proposed to solve this challenge. Subsequently, manganese oxide species (MnO<sub>x</sub>) was photo-deposited on tungsten trioxide (WO<sub>3</sub>) as a proof-of-concept prototype photoanode. Photoelectric structure characterization demonstrated that MnO<sub>x</sub> species were validated to diminish H<sub>2</sub>O<sub>2</sub> oxidation overpotential by increasing the concentration and lifetime of photogenerated holes, accelerating significantly H<sub>2</sub>O<sub>2</sub> oxidation. As a result, the MnO<sub>x</sub>/WO<sub>3</sub> photoanode achieves a lower detection limit of 0.1 mM and a higher sensitivity of 4.81 μA cm<sup>−2</sup> mM<sup>−1</sup> for H<sub>2</sub>O<sub>2</sub> detection respectively, which are 0.125 (0.8 mM) and 1.72 (2.79 μA cm<sup>−2</sup> mM<sup>−1</sup>) times sensitive compared to that of WO<sub>3</sub> photoanode. This work demonstrates a hole enrichment strategy to boost the sensitivity of trace H<sub>2</sub>O<sub>2</sub> analysis.</div></div>\",\"PeriodicalId\":355,\"journal\":{\"name\":\"Journal of Electroanalytical Chemistry\",\"volume\":\"993 \",\"pages\":\"Article 119254\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-05-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Electroanalytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1572665725003285\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665725003285","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Boosting photoelectrochemical detection accuracy of trace H2O2 by inducing holes accumulation on the MnOx/WO3
Restrained by sluggish migration dynamics of holes, the detection sensitivity and limit of an anodic photoelectrochemical (APEC) strategy for trace hydrogen peroxide (H2O2) is generally difficult to meet the demands of the current chemical industry. Herein, interface hole enrichment engineering is proposed to solve this challenge. Subsequently, manganese oxide species (MnOx) was photo-deposited on tungsten trioxide (WO3) as a proof-of-concept prototype photoanode. Photoelectric structure characterization demonstrated that MnOx species were validated to diminish H2O2 oxidation overpotential by increasing the concentration and lifetime of photogenerated holes, accelerating significantly H2O2 oxidation. As a result, the MnOx/WO3 photoanode achieves a lower detection limit of 0.1 mM and a higher sensitivity of 4.81 μA cm−2 mM−1 for H2O2 detection respectively, which are 0.125 (0.8 mM) and 1.72 (2.79 μA cm−2 mM−1) times sensitive compared to that of WO3 photoanode. This work demonstrates a hole enrichment strategy to boost the sensitivity of trace H2O2 analysis.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
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