Wenjing Jiao , Benlin He , Ziyu Wang , Shouhao Sun , Meng Wei , Weilin Liu , Mingran Sun , Haiyan Chen , Haiyan Li , Jialong Duan , Qunwei Tang
{"title":"Reducing oxygen vacancies of MoO3 by polyaniline functionalization for stable and efficient inorganic tri-brominated perovskite solar cells","authors":"Wenjing Jiao , Benlin He , Ziyu Wang , Shouhao Sun , Meng Wei , Weilin Liu , Mingran Sun , Haiyan Chen , Haiyan Li , Jialong Duan , Qunwei Tang","doi":"10.1016/j.mtphys.2024.101514","DOIUrl":null,"url":null,"abstract":"<div><p>The photovoltaic performance of perovskite solar cells (PSCs) is closely dependent on the efficient carrier extraction and transport at the interface. Here, a polyaniline (PANI) functionalized MoO<sub>3</sub> (PANI/MoO<sub>3</sub>) hole transport material (HTM) is exploited to perfect the interface between the perovskite layer and carbon electrode in all-inorganic CsPbBr<sub>3</sub> PSCs. After functionalization with PANI, the p-type behavior and the hole mobility and conductivity of MoO<sub>3</sub> are improved by reducing the oxygen vacancies, which boosts the hole extraction and transport, energy level arrangement at the interface of CsPbBr<sub>3</sub> perovskite/(PANI/MoO<sub>3</sub>) HTM. Meanwhile, the PANI/MoO<sub>3</sub> with rich C–N and N–H groups introduced by PANI passivates the ions trap states of perovskite films by the C–N⋯Pb<sup>2+</sup> (Cs<sup>+</sup>) Lewis acid-base coordination and the N–H⋯Br<sup>−</sup> hydrogen bonding, leading to an effective suppression of non-radiative recombination for improved carrier extraction. As a result, the PANI/MoO<sub>3</sub> HTMs-based CsPbBr<sub>3</sub> PSCs obtain a remarkably increased power conversion efficiency of 10.41 %, in comparison with the efficiency of the original device (6.55 %). In addition, the unencapsulated device with PANI/MoO<sub>3</sub> HTMs shows excellent long-term stability with 93.9 % maintenance of the initial efficiency after storing in air with 85 % relative humidity and at 85 °C for 30 days.</p></div>","PeriodicalId":18253,"journal":{"name":"Materials Today Physics","volume":null,"pages":null},"PeriodicalIF":10.0000,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Physics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2542529324001901","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The photovoltaic performance of perovskite solar cells (PSCs) is closely dependent on the efficient carrier extraction and transport at the interface. Here, a polyaniline (PANI) functionalized MoO3 (PANI/MoO3) hole transport material (HTM) is exploited to perfect the interface between the perovskite layer and carbon electrode in all-inorganic CsPbBr3 PSCs. After functionalization with PANI, the p-type behavior and the hole mobility and conductivity of MoO3 are improved by reducing the oxygen vacancies, which boosts the hole extraction and transport, energy level arrangement at the interface of CsPbBr3 perovskite/(PANI/MoO3) HTM. Meanwhile, the PANI/MoO3 with rich C–N and N–H groups introduced by PANI passivates the ions trap states of perovskite films by the C–N⋯Pb2+ (Cs+) Lewis acid-base coordination and the N–H⋯Br− hydrogen bonding, leading to an effective suppression of non-radiative recombination for improved carrier extraction. As a result, the PANI/MoO3 HTMs-based CsPbBr3 PSCs obtain a remarkably increased power conversion efficiency of 10.41 %, in comparison with the efficiency of the original device (6.55 %). In addition, the unencapsulated device with PANI/MoO3 HTMs shows excellent long-term stability with 93.9 % maintenance of the initial efficiency after storing in air with 85 % relative humidity and at 85 °C for 30 days.
期刊介绍:
Materials Today Physics is a multi-disciplinary journal focused on the physics of materials, encompassing both the physical properties and materials synthesis. Operating at the interface of physics and materials science, this journal covers one of the largest and most dynamic fields within physical science. The forefront research in materials physics is driving advancements in new materials, uncovering new physics, and fostering novel applications at an unprecedented pace.