Li Xin, Ying Zhiqin, Zheng Jingming, Wang Xinlong, Chen Ying, Wu Ming, Xiao Chuanxiao, Sun Jingsong, Shou Chunhui, Yang Zhenhai, Zeng Yuheng, Yang Xi, Ye Jichun
Zhejiang Provincial Engineering Research Center of Energy Optoelectronic Materials and Devices, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201, China.
University of Chinese Academy of Sciences, No.19(A) Yuquan Road, Shijingshan District, Beijing, 100049, China.
Adv Mater. 2023 Jul;35(30):e2211962. doi: 10.1002/adma.202211962. Epub 2023 Jun 6.
Despite the swift rise in power conversion efficiency (PCE) to more than 32%, the instability of perovskite/silicon tandem solar cells is still one of the key obstacles to practical application and is closely related to the residual strain of perovskite films. Herein, a simple surface reconstruction strategy is developed to achieve a global incorporation of butylammonium cations at both surface and bulk grain boundaries by post-treating perovskite films with a mixture of N,N-dimethylformamide and n-butylammonium iodide in isopropanol solvent, enabling strain-free perovskite films with simultaneously reduced defect density, suppressed ion migration, and improved energy level alignment. As a result, the corresponding single-junction perovskite solar cells yield a champion PCE of 21.8%, while maintaining 100% and 81% of their initial PCEs without encapsulation after storage for over 2500 h in N and 1800 h in air, respectively. Remarkably, a certified stabilized PCE of 29.0% for the monolithic perovskite/silicon tandems based on tunnel oxide passivated contacts is further demonstrated. The unencapsulated tandem device retains 86.6% of its initial performance after 306 h at maximum power point (MPP) tracking under continuous xenon-lamp illumination without filtering ultraviolet light (in air, 20-35 °C, 25-75%RH, most often ≈60%RH).
尽管功率转换效率(PCE)迅速提高到32%以上,但钙钛矿/硅串联太阳能电池的不稳定性仍然是实际应用的关键障碍之一,并且与钙钛矿薄膜的残余应变密切相关。在此,开发了一种简单的表面重构策略,通过在异丙醇溶剂中用N,N-二甲基甲酰胺和正丁基碘化铵的混合物对钙钛矿薄膜进行后处理,在表面和体相晶界实现丁基铵阳离子的全局掺入,从而获得无应变的钙钛矿薄膜,同时降低缺陷密度、抑制离子迁移并改善能级排列。结果,相应的单结钙钛矿太阳能电池的最佳PCE为21.8%,在氮气中储存超过2500小时和在空气中储存1800小时后,未封装时分别保持其初始PCE的100%和81%。值得注意的是,基于隧道氧化物钝化接触的单片钙钛矿/硅串联太阳能电池的认证稳定PCE进一步证明为29.0%。在连续氙灯照明(未过滤紫外线,在空气中,20-35°C,25-75%RH,最常见约为60%RH)下最大功率点(MPP)跟踪306小时后,未封装的串联器件保留了其初始性能的86.6%。