钙钛矿(结构)
钝化
齿合度
材料科学
配体(生物化学)
螯合作用
结晶
图层(电子)
能量转换效率
化学工程
纳米技术
光电子学
化学
结晶学
冶金
受体
金属
生物化学
工程类
作者
Baibai Liu,Qian Zhou,Yong Li,Yu Chen,Dongmei He,Danqing Ma,Xiao Han,Ru Li,Ke Yang,Yingguo Yang,Shirong Lu,Xiaodong Ren,Zhengfu Zhang,Liming Ding,Jing Feng,Jianhong Yi,Jiangzhao Chen
标识
DOI:10.1002/anie.202317185
摘要
Abstract The instability of the buried interface poses a serious challenge for commercializing perovskite photovoltaic technology. Herein, we report a polydentate ligand reinforced chelating strategy to strengthen the stability of buried interface by managing interfacial defects and stress. The bis(2,2,2‐trifluoroethyl) (methoxycarbonylmethyl)phosphonate (BTP) is employed to manipulate the buried interface. The C=O, P=O and two −CF 3 functional groups in BTP synergistically passivate the defects from the surface of SnO 2 and the bottom surface of the perovskite layer. Moreover, The BTP modification contributes to mitigated interfacial residual tensile stress, promoted perovskite crystallization, and reduced interfacial energy barrier. The multidentate ligand modulation strategy is appropriate for different perovskite compositions. Due to much reduced nonradiative recombination and heightened interface contact, the device with BTP yields a promising power conversion efficiency (PCE) of 24.63 %, which is one of the highest efficiencies ever reported for devices fabricated in the air environment. The unencapsulated BTP‐modified devices degrade to 98.6 % and 84.2 % of their initial PCE values after over 3000 h of aging in the ambient environment and after 1728 h of thermal stress, respectively. This work provides insights into strengthening the stability of the buried interface by engineering multidentate chelating ligand molecules.
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