Hui Liu, Jisen Zhang, Wenqiang Ding, Yidan An, Miao Zhang, Songyang Yuan, Guanhua Ren, Ziyao Yue, Guangruixing Zou, Nan Zhang, Quanrun Qiu, Sai-Wing Tsang, Tingting Shi, Guodan Wei, Hin-Lap Yip
Mixed tin-lead (Sn-Pb) perovskite solar cells (PSCs) have great potential for photovoltaics and infrared photodetector (PD) applications. However, their performance and reliability are severely limited by non-radiative recombination, both within the perovskite bulk and at the interface between the perovskite and hole transporting layer (HTL). In HTL-free architectures, the buried perovskite/ITO interface becomes the dominant extraction and recombination bottleneck, yet remains insufficiently engineered. Herein, we report an efficient HTL-free mixed Sn-Pb optoelectronic device by introducing isoniazid (INH) into the perovskite film (FA0.6MA0.3Cs0.1Pb0.5Sn0.5I3) to in situ form a dipole interface and establish a built-in electric field, thereby suppressing the interface/bulk non-radiative recombination and promoting hole extraction. The INH molecule can coordinate with Sn2+ to modulate film crystallization, and the hydrazide group acts as a potent reducing agent, mitigating the Sn2+ oxidation and passivating the defects. As a result, the optimized HTL-free Sn-Pb PSCs achieved a champion power conversion efficiency (PCE) of 23.71%, with improved stability that retained 80% of their initial efficiency after 2250 h in an N2 glovebox. Additionally, this strategy enabled high-performance HTL-free PDs with a remarkable specific detectivity beyond 1014 Jones at 920 nm. This work provides a strategic pathway for developing efficient HTL-free Sn-Pb perovskite optoelectronic devices.