Jingping Li, Suding Yan, Jiaxi Wu, Qiang Cheng, Kai Wang
{"title":"Improving hydrogen peroxide photosynthesis over inorganic/organic S-scheme photocatalyst with LiFePO4","authors":"Jingping Li, Suding Yan, Jiaxi Wu, Qiang Cheng, Kai Wang","doi":"10.1016/j.actphy.2025.100104","DOIUrl":null,"url":null,"abstract":"<div><div>With the rapid development of new energy industries, the utilization of waste batteries has attracted the attention of researchers. Developing a hydrogen peroxide photosynthesis system with battery recycling materials as photocatalysts presents a significant challenge. In this study, an ultrasonic self-assembly technique is employed to integrate LiFePO<sub>4</sub> (LFPO) nanoparticles, derived from spent batteries, with g-C<sub>3</sub>N<sub>4</sub> (CN) nanosheets, thereby creating an inorganic/organic S-scheme photocatalyst for the production of H<sub>2</sub>O<sub>2</sub>. <em>In situ</em> analyses using X-ray photoelectron spectroscopy (XPS) and Kelvin probe force microscopy (KPFM) demonstrate that the interaction between LFPO and CN facilitates the development of an internal electric field (IEF), which in turn gives rise to a distinctive S-scheme charge transfer mechanism. Combining electron spin resonance spectroscopy, radical-trapping experiments, and <em>in situ</em> DRIFTS spectra, three pathways for H<sub>2</sub>O<sub>2</sub> formation are identified. Benefited from enhanced carrier separation, strong redox power, and multichannel H<sub>2</sub>O<sub>2</sub> formation, the optimal composite shows an impressive H<sub>2</sub>O<sub>2</sub>-production rate of 3.22 mol g<sup>−1</sup> h<sup>−1</sup> under simulated solar irradiation. This research provides a potential method to investigate a sustainable H<sub>2</sub>O<sub>2</sub> photosynthesis pathway by designing S-scheme heterojunctions from spent battery materials.</div></div>","PeriodicalId":6964,"journal":{"name":"物理化学学报","volume":"41 9","pages":"Article 100104"},"PeriodicalIF":10.8000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"物理化学学报","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1000681825000608","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
With the rapid development of new energy industries, the utilization of waste batteries has attracted the attention of researchers. Developing a hydrogen peroxide photosynthesis system with battery recycling materials as photocatalysts presents a significant challenge. In this study, an ultrasonic self-assembly technique is employed to integrate LiFePO4 (LFPO) nanoparticles, derived from spent batteries, with g-C3N4 (CN) nanosheets, thereby creating an inorganic/organic S-scheme photocatalyst for the production of H2O2. In situ analyses using X-ray photoelectron spectroscopy (XPS) and Kelvin probe force microscopy (KPFM) demonstrate that the interaction between LFPO and CN facilitates the development of an internal electric field (IEF), which in turn gives rise to a distinctive S-scheme charge transfer mechanism. Combining electron spin resonance spectroscopy, radical-trapping experiments, and in situ DRIFTS spectra, three pathways for H2O2 formation are identified. Benefited from enhanced carrier separation, strong redox power, and multichannel H2O2 formation, the optimal composite shows an impressive H2O2-production rate of 3.22 mol g−1 h−1 under simulated solar irradiation. This research provides a potential method to investigate a sustainable H2O2 photosynthesis pathway by designing S-scheme heterojunctions from spent battery materials.