Even though ZnO is commonly used as the ETL in the perovskite solar cell (PSC), the reactivity of perovskite deposited thereupon limits its performance. Herein, an ethylene diamine tetraacetic acid-complexed ZnO (E-ZnO) is successfully developed as a significantly improved electron selective layer (ESLs) in perovskite device. It is found that E-ZnO exhibits higher electron mobility and better matched energy level with perovskite compared to ZnO. In addition, in order to eliminate the proton transfer reaction at the ZnO/perovskite interface, a high quality perovskite film fabrication process that requires neither annealing nor antisolvent is developed. By taking advantages of both E-ZnO and the new process, the highest efficiency of 20.39% is obtained for PSCs based on E-ZnO. Moreover, the efficiency of unencapsulated PSCs with E-ZnO retains 95% of its initial value exposed in an ambient atmosphere after 3604 h. This work provides a feasible path toward high performance of PSCs, and it is believed that the present work will facilitate transition of perovskite photovoltaics in flexible and tandem devices since the annealing- and antisolvent-free technology.
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http://dx.doi.org/10.1002/advs.202002860 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Institute of New Energy Technology, College of Physics and Optoelectronic Engineering, Jinan University, Guangzhou 510632, Guangdong, China.
Formamidinium-based perovskites (FA perovskites) often incorporate methylammonium chloride (MACl) to stabilize the α-FAPbI phase and prevent formation of the δ phase. However, MACl undergoes deprotonation and reacts with FA, leading to the generation of unstable byproducts that can cause component degradation and negatively impact the device performance. In this study, we introduce ethylenediaminetetramethylenephosphonic acid as a corrosion inhibitor, which effectively prevents the formation of these byproducts and stabilizes α-FAPbI.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Shandong University of Science and Technology, Institute of Carbon Neutrality, College of Chemical and Biological Engineering, No 579 Qianwangang Road, Huangdao District, 266590, Qingdao, CHINA.
Traditionally weak buried interaction without customized chemical bonding always goes against the formation of high-quality perovskite film that highly determines the efficiency and stability of perovskite solar cells. To address this issue, herein, we propose a bimolecular nucleophilic substitution reaction (SN2) driving strategy to idealize the robust buried interface by simultaneously decorating underlying substrate and functionalizing [PbX6]4- octahedral framework with iodoacetamide and thiol molecules, respectively. Theoretical and experimental results demonstrate that a strong SN2 reaction between exposed halogen and thiol group in two molecules occurs, which not only benefits the reinforcement of buried adhesion, but also triggers target-point-oriented crystallization, synergistically upgrading the upper perovskite film quality and accelerating interfacial charge extraction-transfer behavior.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Southern University of Science and Technology, Department of Mechanical and Energy Engineering, 1088 Xueyuan Blvd, Nanshan District, 518055, Shenzhen, CHINA.
The escape of organic cations over time from defective perovskite interface leads to non-stoichiometric terminals, significantly affecting the stability of perovskite solar cells (PSCs). How to stabilize the interface composition under environmental stress remains a grand challenge. To address this issue, we utilize thiol-functionalized particles as a "seed" and conduct in situ polymerization of 2,2,3,4,4,4-hexafluorobutyl methacrylate (HFMA) as a "root" at the bottom of the perovskite layer.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Guangxi Key Laboratory of Optical and Electronic Material and Devices, School of Materials Science and Engineering, Guilin University of Technology, 12 Jiangan Road, Guilin, Guangxi 541004, China.
Sticker-type transparent antireflective film (STAF) is applied to perovskite solar cells (PSCs) to reduce the reflection and improve the light-trapping ability of PSCs. However, the development of STAF is hindered by many factors, such as expensive materials, low actual service life, unsatisfactory antireflective effect, and a lack of research on stability. This work proposes an ultraviolet (UV)-resistant enhanced sticker-type nanostructure acrylic resin antireflective film (SNAAF), which is applied to the incident surface of PSCs.
View Article and Find Full Text PDFNanomicro Lett
January 2025
CAS Key Laboratory of Organic Solids, Institute of Chemistry, Beijing National Laboratory for Molecular Sciences, Chinese Academy of Sciences, Beijing, 100049, People's Republic of China.
Finding ways to produce dense and smooth perovskite films with negligible defects is vital for achieving high-efficiency perovskite solar cells (PSCs). Herein, we aim to enhance the quality of the perovskite films through the utilization of a multifunctional additive in the perovskite anti-solvent, a strategy referred to as anti-solvent additive engineering. Specifically, we introduce ortho-substituted-4'-(4,4″-di-tert-butyl-1,1':3',1″-terphenyl)-graphdiyne (o-TB-GDY) as an AAE additive, characterized by its sp/sp-cohybridized and highly π-conjugated structure, into the anti-solvent.
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