{"title":"Functionalized Organic/Polymeric Materials for Perovskite and Organic Solar Cells","authors":"Haiyang Chen, Yege Jing, Juan Zhu, Yaowen Li","doi":"10.1021/accountsmr.5c00344","DOIUrl":null,"url":null,"abstract":"<p>Perovskite solar cells (pero-SCs)\r\nand organic solar cells (OSCs),\r\nowing to their solution processability, lightweight form factors,\r\nand exceptional mechanical flexibility, have emerged as leading contenders\r\nto complement silicon photovoltaics in distributed energy systems.\r\nIn recent years, rapid progress has pushed the power conversion efficiencies\r\nof rigid laboratory-scale pero-SCs beyond 27% and OSCs above 21%.\r\nYet, translating these achievements into practical deployment requires\r\nsimultaneous advances in flexibility, large-area manufacturability,\r\nand long-term operational stability. The chemically programmable nature\r\nof organic and polymeric materials provides a powerful platform for\r\naddressing these challenges. Their tunable molecular structures enable\r\nthe rational design of functional motifs tailored to the specific\r\nneeds of different thin-film layers, offering “function-on-demand”\r\ncapabilities. Such functionalized materials can be engineered to serve\r\nas key components in printed flexible transparent electrodes, charge-transport\r\nlayers, and active layers. By introducing well-defined redox-active\r\nunits, dynamically cross-linkable groups, self-assembling cores, and\r\nmoieties that modulate solution viscosity and aggregation behavior,\r\nresearchers can simultaneously improve mechanical robustness, film\r\nuniformity, interfacial energetics, and environmental stability. In\r\nthis Account, we highlight recent advances in achieving stable, flexible,\r\nand large-area pero-SCs and OSCs through use of functionalized organic\r\nand polymeric materials, with emphasis on key contributions from our\r\ngroup. We summarize the underlying design principles, elucidate structure–property–performance\r\ncorrelations in representative material systems, and illustrate how\r\nfunctionally tailored molecules can bridge the gap between molecular-level\r\ndesign and device-level performance. Finally, we offer our perspective\r\non remaining challenges and future research directions toward practical\r\nimplementation of flexible and scalable perovskite and organic photovoltaics.</p>","PeriodicalId":72040,"journal":{"name":"Accounts of materials research","volume":"7 6","pages":"549–562"},"PeriodicalIF":14.1000,"publicationDate":"2026-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of materials research","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/accountsmr.5c00344","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/17 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Perovskite solar cells (pero-SCs)
and organic solar cells (OSCs),
owing to their solution processability, lightweight form factors,
and exceptional mechanical flexibility, have emerged as leading contenders
to complement silicon photovoltaics in distributed energy systems.
In recent years, rapid progress has pushed the power conversion efficiencies
of rigid laboratory-scale pero-SCs beyond 27% and OSCs above 21%.
Yet, translating these achievements into practical deployment requires
simultaneous advances in flexibility, large-area manufacturability,
and long-term operational stability. The chemically programmable nature
of organic and polymeric materials provides a powerful platform for
addressing these challenges. Their tunable molecular structures enable
the rational design of functional motifs tailored to the specific
needs of different thin-film layers, offering “function-on-demand”
capabilities. Such functionalized materials can be engineered to serve
as key components in printed flexible transparent electrodes, charge-transport
layers, and active layers. By introducing well-defined redox-active
units, dynamically cross-linkable groups, self-assembling cores, and
moieties that modulate solution viscosity and aggregation behavior,
researchers can simultaneously improve mechanical robustness, film
uniformity, interfacial energetics, and environmental stability. In
this Account, we highlight recent advances in achieving stable, flexible,
and large-area pero-SCs and OSCs through use of functionalized organic
and polymeric materials, with emphasis on key contributions from our
group. We summarize the underlying design principles, elucidate structure–property–performance
correlations in representative material systems, and illustrate how
functionally tailored molecules can bridge the gap between molecular-level
design and device-level performance. Finally, we offer our perspective
on remaining challenges and future research directions toward practical
implementation of flexible and scalable perovskite and organic photovoltaics.