{"title":"Sustainable Recycling of Perovskite Solar Cells: Green Solvent-Based Recovery of ITO Substrates","authors":"Sun-Ju Kim, Eun-Ju Jeong, Ji-Youn Seo","doi":"10.1002/kin.21771","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Perovskite solar cells (PSCs) emerge as a leading next-generation photovoltaic (PV) technology, with power conversion efficiencies (PCEs) reaching 26.7% for single cells and 36.1% for hybrid tandem cells. As commercialization progresses, the inverted (p–i–n) structure of PSCs gains attention due to its enhanced thermal stability, lower moisture sensitivity, and reduced processing temperatures compared to the conventional (n–i–p) structure. However, sustainability concerns, particularly regarding production costs and end-of-life disposal, become increasingly critical. Recycling PSCs provides a viable solution to these challenges by recovering valuable indium tin oxide (ITO) substrates, which significantly impact material costs. Existing recycling methods for conventional PSCs often use toxic solvents like chlorobenzene (CB) and <i>N</i>,<i>N</i>-dimethylformamide (DMF), posing environmental and health risks. This study introduces an eco-friendly recycling process for ITO-based inverted PSCs using acetone as a green solvent. The results show that recycled ITO substrates maintain their physical, electrical, and optical properties without significant degradation in PSC performance, even after multiple recycling cycles. This green solvent-based approach not only preserves device efficiency but also supports future environmental regulations, highlighting its potential in promoting sustainable and cost-effective PV technologies.</p>\n </div>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":"57 4","pages":"235-241"},"PeriodicalIF":1.5000,"publicationDate":"2024-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Chemical Kinetics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/kin.21771","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Perovskite solar cells (PSCs) emerge as a leading next-generation photovoltaic (PV) technology, with power conversion efficiencies (PCEs) reaching 26.7% for single cells and 36.1% for hybrid tandem cells. As commercialization progresses, the inverted (p–i–n) structure of PSCs gains attention due to its enhanced thermal stability, lower moisture sensitivity, and reduced processing temperatures compared to the conventional (n–i–p) structure. However, sustainability concerns, particularly regarding production costs and end-of-life disposal, become increasingly critical. Recycling PSCs provides a viable solution to these challenges by recovering valuable indium tin oxide (ITO) substrates, which significantly impact material costs. Existing recycling methods for conventional PSCs often use toxic solvents like chlorobenzene (CB) and N,N-dimethylformamide (DMF), posing environmental and health risks. This study introduces an eco-friendly recycling process for ITO-based inverted PSCs using acetone as a green solvent. The results show that recycled ITO substrates maintain their physical, electrical, and optical properties without significant degradation in PSC performance, even after multiple recycling cycles. This green solvent-based approach not only preserves device efficiency but also supports future environmental regulations, highlighting its potential in promoting sustainable and cost-effective PV technologies.
期刊介绍:
As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.