退火(玻璃)
材料科学
薄膜
太阳能电池
碘化物
钙钛矿(结构)
四氢呋喃
钙钛矿太阳能电池
光电子学
化学工程
纳米技术
结晶学
化学
无机化学
复合材料
有机化学
工程类
溶剂
作者
Farhad Azad,Thidarat Supasai,Annafi Ado Yaro,Kay Thi Soe,Non Thongprong,Ekkaphop Ketsombun,Navaphun Kayunkid,Ratchadaporn Supruangnet,Narong Chanlek,Patrick Chapon,Nopporn Rujisamphan
标识
DOI:10.1021/acsmaterialslett.3c01606
摘要
We demonstrate a functional method to achieve surface passivation and construct a two-dimensional (2D) layer on a three-dimensional (3D) perovskite, eliminating the need for subsequent annealing steps. A key process is the integration of a single methylammonium lead iodide (MAPbI3) crystal with butylammonium iodide (BAI) in tetrahydrofuran. Density functional theory calculations reveal that the synergy between BA+ cations and Pb–I octahedral structures enables the formation of a distinct 2D layered framework. MA+ and BA+ exhibit adsorption energies of −5.519 and −5.925 eV, respectively, at MA vacancies on the perovskite surface. This finding indicates that BAI passivation induces surface-healing effects, increasing surface and device stability. The I– components of BAI also replace imperfections at the perovskite interface, affording considerably reduced deep-level anomalies and mitigating nonradiative recombination. This theoretical perspective is supported experimentally via X-ray photoelectron spectroscopy and glow discharge optical emission spectroscopy. BAI passivation and 2D-BA2PbI4 capping lowers work functions for 3D perovskite surfaces, registering at approximately 0.158 and 0.173 eV, respectively, which are lower than those of the control 3D film. Within the 2D/3D perovskite configuration, 2D-BA2PbI4 capping considerably increases the open-circuit voltage in solar cells. In comparison, devices with BAI-enhanced interfaces show improved durability with promise for solar cell applications.
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