材料科学
硒
带隙
纳米技术
光电子学
工程物理
冶金
工程类
作者
Qingxiang Liu,Xia Wang,Zongbao Li,Wenbo Lu,Xin Wen,Xioayan An,Mingjie Feng,Hui‐Juan Yan,Jin‐Song Hu,Ding‐Jiang Xue
标识
DOI:10.1002/adma.202410835
摘要
The recent surge in tandem solar cells and indoor photovoltaics has renewed interest in selenium (Se), the world's first photovoltaic material, due to its intrinsic wide bandgap of ≈1.9 eV, high stability, and non-toxicity in small quantities when applied in photovoltaics. However, with a 1D chained crystal structure, Se tends to grow crystalline films with a lying orientation-chains parallel to substrates arising from the low surface energy; this results in poor carrier transport across chains held together by weak van der Waals forces. Here a substrate-heating strategy that facilitates the interfacial bonding between Se and substrate is introduced, enabling the growth of Se films with a standing orientation-chains perpendicular to substrates. This achieves efficient carrier transport along covalently bonded chains. The resulting Se films thereby exhibit a fourfold increase in carrier mobility compared to lying-oriented Se films. Consequently, Se solar cells are achieved with the highest power conversion efficiency of 8.1% under AM1.5G 1-sun illumination. The unencapsulated devices exhibit negligible efficiency loss after 1 000 h of storage under ambient conditions.
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