Formamidinium lead triiodide (FAPbI) has received significant attention in the field of perovskite solar cells (PSCs) owing to its excellent optoelectronic properties and high thermal stability. However, the photoactive α-FAPbI perovskites are highly susceptible to degradation into non-perovskite δ-FAPbI phases, especially under humid conditions, which severely diminishes the device performance of FAPbI PSCs. Here, we propose an interfacial seeding strategy for regulating crystallization and stabilizing α-FAPbI perovskites in humid air. By post-treating an antisolvent-free, air-processed perovskite wet film with inorganic cesium lead triiodide (CsPbI) nanocrystals, a functional seed layer is formed that effectively mitigates the erosion by humid air while facilitating the conversion of intermediates to the α-FAPbI phase. The interfacial seed-modified FAPbI perovskite films exhibit improved crystal quality and denser morphology. As a result, the efficiency of all-air-processed carbon-based PSCs is improved from 15.90% for the control to 18.04%. In addition, the unencapsulated PSCs based on interfacial seed-modified FAPbI films show improved environmental stability compared to their control counterparts, maintaining 80% of their initial efficiency after 60 days.
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http://dx.doi.org/10.1039/d4dt03120b | DOI Listing |
ACS 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.
View Article and Find Full Text PDFNano Lett
January 2025
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Solar-powered electrochemical NH synthesis offers the benefits of sustainability and absence of CO emissions but suffers from a poor solar-to-ammonia yield rate (SAY) due to a low NH selectivity, large bias caused by the sluggish oxygen evolution reaction, and low photocurrent in the corresponding photovoltaics. Herein, a highly efficient photovoltaic-electrocatalytic system enabling high-rate solar-driven NH synthesis was developed. A high-performance Ru-doped Co nanotube catalyst was used to selectively promote the nitrite reduction reaction (NORR), exhibiting a faradaic efficiency of 99.
View Article and Find Full Text PDFSmall
January 2025
Engineering Research Center of Electronic Information Materials and Devices (Ministry of Education), Guangxi Key Laboratory of Information Materials, School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin, 541004, China.
In recent years, carbon-based printable mesoscopic perovskite solar cells (p-MPSCs) without hole transport layers have garnered considerable interest because of their outstanding benefits in terms of stability and cost. However, the use of carbon electrodes instead of hole transport materials and noble metal electrodes leads to energy level mismatch, which limits the power conversion efficiency (PCE) of p-MPSCs. In this work, a molecular doping strategy is proposed employing cyclopentylmethanamine to passivate surface and subsurface crystal defects in perovskite layers while inducing an energy shift toward the p-type in the perovskite region within carbon electrodes.
View Article and Find Full Text PDFSci Rep
January 2025
Facultad de Química, Materiales-Energía, Universidad Autónoma de Querétaro, Santiago de Querétaro, C.P.76010, Querétaro, México.
ABSchalcogenide perovskites (CPs) are emerging as promising alternatives to lead halide perovskites due to their unique properties. However, their bandgap exceeds the Shockley-Queisser limit. By substituting S with Se, the bandgap is significantly reduced, shifting it from the visible into the near-infrared region.
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