Chen Zukang, Cao Shuguang, Luo Shizi, Gutsev Lavrenty G, Chen Xiaoli, Ozerova Victoria V, Emelianov Nikita A, Slesarenko Nikita A, Bolshakova Valeria S, Zheng Yupeng, Bi Zhuoneng, Aldoshin Sergey M, Troshin Pavel A, Ramachandran Bala R, Gutsev Gennady L, Hsu Hsien-Yi, Xue Qifan, Xu Xueqing
Guangzhou Institute of Energy Conversion, Key Laboratory of Renewable Energy, Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Chinese Academy of Sciences, Guangzhou 510640, PR China.
University of Science and Technology of China, Hefei 230026, PR China.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50706-50716. doi: 10.1021/acsami.4c09850. Epub 2024 Sep 16.
Current development of inverted p-i-n perovskite solar cells (PSCs), with nickel oxide as the hole transport layer, is progressing toward lower net costs, higher efficiencies, and superior stabilities. Unfortunately, the high density of defect-based traps on the surface of perovskite films significantly limits the photoelectric conversion efficiency and operational stability of perovskite solar cells. Finding cost-effective interface modifiers is crucial for the further commercial development of p-i-n PSCs. In the present work, we report a passivation strategy using a multifunctional molecule, benzocaine hydrochloride (BHC), which is shown to reduce defect density and enhance the photovoltaic performance and stability of the resultant p-i-n PSCs. It has been revealed that BHC strongly interacts with perovskite precursor components and triggers the evolution of the perovskite absorber film morphology and enables improved surface energy level alignment, thus promoting charge carrier transport and extraction. These properties are beneficial for improving open-circuit voltage () and fill factor (FF). Our results show that the photoelectric conversion efficiency (PCE) of p-i-n PSCs with nickel oxide as the hole transport layer increased from an initial 20.0% to 22.1% after being passivated with BHC, and these passivated devices also exhibited improved stability. DFT calculations reveal the unusual ability of the BHC passivant to improve band alignment while also preventing the accumulation of holes at the interface. In this work, the advantages of BHC passivation are demonstrated by linking theoretical calculations with optical and electrical characterizations.
以氧化镍作为空穴传输层的倒置p-i-n钙钛矿太阳能电池(PSC)目前的发展正朝着更低的净成本、更高的效率和更优异的稳定性迈进。不幸的是,钙钛矿薄膜表面基于缺陷的陷阱高密度显著限制了钙钛矿太阳能电池的光电转换效率和运行稳定性。找到具有成本效益的界面改性剂对于p-i-n PSC的进一步商业发展至关重要。在本工作中,我们报告了一种使用多功能分子盐酸苯佐卡因(BHC)的钝化策略,结果表明该策略可降低缺陷密度,并提高所得p-i-n PSC的光伏性能和稳定性。研究发现,BHC与钙钛矿前驱体组分强烈相互作用,触发钙钛矿吸收层薄膜形态的演变,并实现改善的表面能级排列,从而促进电荷载流子的传输和提取。这些特性有利于提高开路电压()和填充因子(FF)。我们的结果表明,以氧化镍作为空穴传输层的p-i-n PSC在用BHC钝化后,其光电转换效率(PCE)从最初的20.0%提高到了22.1%,并且这些钝化器件还表现出了更好的稳定性。密度泛函理论(DFT)计算揭示了BHC钝化剂在改善能带排列同时还能防止界面处空穴积累的非凡能力。在本工作中,通过将理论计算与光学和电学表征相结合,证明了BHC钝化的优势。