Gong Xiu, Guan Li, Li Qingwei, Li Yan, Zhang Tao, Pan Han, Sun Qiang, Shen Yan, Grätzel Carole, Zakeeruddin Shaik M, Grätzel Michael, Wang Mingkui
Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, Hubei 430074, P.R. China.
College of Physics Science and Technology, Hebei University, 180 Wusi E Road, Baoding 071000, P.R. China.
Sci Adv. 2020 Apr 10;6(15):eaay5661. doi: 10.1126/sciadv.aay5661. eCollection 2020 Apr.
Black phosphorus quantum dots (BPQDs) are proposed as effective seed-like sites to modulate the nucleation and growth of CsPbIBr perovskite crystalline thin layers, allowing an enhanced crystallization and remarkable morphological improvement. We reveal that the lone-pair electrons of BPQDs can induce strong binding between molecules of the CsPbIBr precursor solution and phosphorus atoms stemming from the concomitant reduction in coulombic repulsion. The four-phase transition during the annealing process yields an α-phase CsPbIBr stabilized by BPQDs. The BPQDS/CsPbIBr core-shell structure concomitantly reinforces a stable CsPbIBr crystallite and suppresses the oxidation of BPQDs. Consequently, a power conversion efficiency of 15.47% can be achieved for 0.7 wt % BPQDs embedded in CsPbIBr film-based devices, with an enhanced cell stability, under ambient conditions. Our finding is a decisive step in the exploration of crystallization and phase stability that can lead to the realization of efficient and stable inorganic perovskite solar cells.
黑磷量子点(BPQDs)被认为是有效的类种子位点,可调节CsPbIBr钙钛矿晶体薄膜的成核和生长,从而促进结晶并显著改善形态。我们发现,BPQDs的孤对电子可诱导CsPbIBr前驱体溶液分子与磷原子之间形成强结合,这源于库仑排斥力的降低。退火过程中的四相转变产生了由BPQDs稳定的α相CsPbIBr。BPQDs/CsPbIBr核壳结构同时增强了CsPbIBr微晶的稳定性,并抑制了BPQDs的氧化。因此,在环境条件下,嵌入CsPbIBr薄膜器件中的0.7 wt% BPQDs可实现15.47%的功率转换效率,且电池稳定性增强。我们的发现是探索结晶和相稳定性的决定性一步,这可能会促成高效稳定的无机钙钛矿太阳能电池的实现。