钝化
钙钛矿(结构)
材料科学
光伏
光电子学
卤化物
能量转换效率
空位缺陷
甲脒
带隙
载流子寿命
离子
图层(电子)
碘化物
光致发光
晶界
光伏系统
氯化物
降级(电信)
钙钛矿太阳能电池
纳米技术
作者
Dan Xu,Jiazhuo Nie,Zhelu Hu,Z. Chen
标识
DOI:10.1021/acsami.5c22974
摘要
Wide-bandgap (1.68 eV) perovskite solar cells (PSCs) are considered promising candidates for indoor photovoltaics due to their favorable optical properties. However, their power conversion efficiency (PCE) is significantly constrained by large open-circuit voltage (VOC) losses, which primarily originate from intrinsic halide vacancy defects and uncoordinated Pb2+ located at the surface and grain boundaries of the perovskite films. Additionally, the energy level mismatches at the perovskite/electron transport layer (ETL) interface further aggravate VOC losses by promoting nonradiative recombination. Herein, we report a synergistic dual-halide interface passivation strategy based on methylammonium iodide (MAI) and methylammonium chloride (MACl), in which the two halides play complementary and mechanistically distinct roles. MAI effectively reacts with and converts residual surface PbI2 into the perovskite phase, while simultaneously passivating iodine-related vacancy defects. In parallel, MACl induces beneficial chloride incorporation at the interface, enabling slight bandgap broadening and producing a favorable vacuum-level shift that optimizes energy-level alignment between the perovskite and electron transport layer. When applied together, MAI and MACl deliver a cooperative passivation effect, substantially suppressing nonradiative recombination, prolonging carrier lifetimes, and facilitating more efficient charge extraction. As a result, the optimized 1.68 eV PSCs achieve a notable PCE of 20.41% with a VOC of 1.262 V under standard AM 1.5G illumination, surpassing the untreated counterparts that achieve 18.48% with a VOC of 1.169 V. More importantly, under indoor lighting conditions, the modified PSCs exhibit outstanding performance, delivering PCEs of 36.74 and 32.36% under 1000 and 200 lx LED illumination, respectively, demonstrating their strong potential for indoor photovoltaics.
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