异质结
钙钛矿(结构)
光伏
材料科学
晶界
配体(生物化学)
纳米技术
格子(音乐)
光电子学
联轴节(管道)
热稳定性
图层(电子)
溴化铵
结构稳定性
作者
Xiaoming Chang,Yanping Liu,Muhammad Iqbal Syauqi,Gongmin Xu,Randi Azmi,Thomas D. Anthopoulos
标识
DOI:10.1021/acsenergylett.5c03310
摘要
The operational stability of perovskite solar cells is limited by defects and instabilities at grain boundaries and buried interfaces in three-dimensional absorbers. Forming 3D/low-dimensional (LD) heterojunctions can improve both efficiency and durability, yet most LD layers use ammonium ligands that bind weakly to the lattice and can deprotonate, causing the LD layer to degrade under heat and illumination. This Perspective highlights amidinium-based organic ligands as a promising alternative for constructing more robust LD capping layers. Their planar, multivalent, resonance-stabilized headgroups enable stronger lattice interactions and reduced deprotonation. Although still emerging, tailoring the ligand tail provides a versatile handle to tune dimensionality, interfacial energetics, strain, and electronic coupling toward efficient, stable LD perovskite heterojunction photovoltaics.
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