钙钛矿(结构)
钝化
材料科学
轨道能级差
能量转换效率
紫外光电子能谱
X射线光电子能谱
甲脒
工作职能
密度泛函理论
开路电压
光电子学
化学工程
纳米技术
化学
电压
计算化学
有机化学
图层(电子)
工程类
物理
量子力学
分子
作者
Lisha Xie,Xuhong Zhao,Jianwei Wang,Jun Li,Chang Liu,Shurong Wang,Qinye Bao,Mengjin Yang,Xiaobin Niu,Feng Hao,Ziyi Ge
出处
期刊:InfoMat
[Wiley]
日期:2022-10-18
卷期号:5 (2)
被引量:31
摘要
Abstract Functional additives have recently been regarded as emerging candidates to improve the performance and stability of perovskite solar cells (PSCs). Herein, nicotinamide (N), 2‐chloronicotinamide (2Cl), and 6‐chloronicotinamide (6Cl) were employed as O‐ligands to facilitate the deposition of MAPbI 3 (MA = methylammonium) and MA‐free FA 0.88 Cs 0.12 PbI 2.64 Br 0.36 (FA = formamidinium) perovskite films by multifunctional anchoring. By density functional theory (DFT) calculations and ultraviolet photoelectron spectroscopy (UPS) measurements, it is identified that the highest occupied molecular orbital (HOMO) level for additive modified MAPbI 3 perovskite could reduce the voltage deficit for hole extraction. Moreover, due to the most favorable charge distribution and significant improvements in charge mobility and defect passivation, the power conversion efficiency (PCE) of 2Cl‐MAPbI 3 PSCs was significantly improved from 19.32% to 21.12%. More importantly, the two‐dimensional grazing‐incidence wide‐angle X‐ray scattering (GIWAXS) analysis showed that PbI 2 defects were effectively suppressed and femtosecond transient absorption (TA) spectroscopy demonstrated that the trap‐assisted recombination at grain boundaries was effectively inhibited in the 2Cl‐MA‐free film. As a result, the thermally stable 2Cl‐MA‐free PSCs achieved a remarkable PCE of 23.13% with an open‐circuit voltage ( V oc ) of 1.164 V and an ultrahigh fill factor (FF) of 85.7%. Our work offers a practical strategy for further commercializing stable and efficient PSCs. image
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