Li Lin, Wei Mingyang, Carnevali Virginia, Zeng Haipeng, Zeng Miaomiao, Liu Ranran, Lempesis Nikolaos, Eickemeyer Felix Thomas, Luo Long, Agosta Lorenzo, Dankl Mathias, Zakeeruddin Shaik M, Roethlisberger Ursula, Grätzel Michael, Rong Yaoguang, Li Xiong
Michael Grätzel Center for Mesoscopic Solar Cells, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, 430074, China.
Beijing Academy of Science and Technology, Beijing, 100089, China.
Adv Mater. 2024 Mar;36(13):e2303869. doi: 10.1002/adma.202303869. Epub 2023 Dec 29.
High-performance perovskite solar cells (PSCs) typically require interfacial passivation, yet this is challenging for the buried interface, owing to the dissolution of passivation agents during the deposition of perovskites. Here, this limitation is overcome with in situ buried-interface passivation-achieved via directly adding a cyanoacrylic-acid-based molecular additive, namely BT-T, into the perovskite precursor solution. Classical and ab initio molecular dynamics simulations reveal that BT-T spontaneously may self-assemble at the buried interface during the formation of the perovskite layer on a nickel oxide hole-transporting layer. The preferential buried-interface passivation results in facilitated hole transfer and suppressed charge recombination. In addition, residual BT-T molecules in the perovskite layer enhance its stability and homogeneity. A power-conversion efficiency (PCE) of 23.48% for 1.0 cm inverted-structure PSCs is reported. The encapsulated PSC retains 95.4% of its initial PCE following 1960 h maximum-power-point tracking under continuous light illumination at 65 °C (i.e., ISOS-L-2I protocol). The demonstration of operating-stable PSCs under accelerated ageing conditions represents a step closer to the commercialization of this emerging technology.
高性能钙钛矿太阳能电池(PSC)通常需要界面钝化,然而由于钝化剂在钙钛矿沉积过程中溶解,这对掩埋界面来说具有挑战性。在此,通过直接向钙钛矿前驱体溶液中添加一种基于氰基丙烯酸的分子添加剂(即BT-T)实现原位掩埋界面钝化,克服了这一限制。经典和从头算分子动力学模拟表明,在氧化镍空穴传输层上形成钙钛矿层的过程中,BT-T可能会在掩埋界面处自发自组装。优先的掩埋界面钝化导致空穴转移更容易且电荷复合受到抑制。此外,钙钛矿层中残留的BT-T分子增强了其稳定性和均匀性。报道了1.0平方厘米倒置结构PSC的功率转换效率(PCE)为23.48%。在65°C连续光照下进行1960小时最大功率点跟踪(即ISOS-L-2I协议)后,封装的PSC保留了其初始PCE的95.4%。在加速老化条件下运行稳定的PSC的示范代表着这项新兴技术向商业化又迈进了一步。