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Crystallization Control Based on the Regulation of Solvent–Perovskite Coordination for High-Performance Ambient Printable FAPbI3 Perovskite Solar Cells
Advanced Materials ( IF 27.4 ) Pub Date : 2023-10-12 , DOI: 10.1002/adma.202307583 Yachao Du 1 , Qingwen Tian 1 , Shiqiang Wang 1 , Lei Yin 1 , Chuang Ma 1 , Zhiteng Wang 1 , Lei Lang 1 , Yingguo Yang 2 , Kui Zhao 1 , Shengzhong Frank Liu 1, 3, 4
Advanced Materials ( IF 27.4 ) Pub Date : 2023-10-12 , DOI: 10.1002/adma.202307583 Yachao Du 1 , Qingwen Tian 1 , Shiqiang Wang 1 , Lei Yin 1 , Chuang Ma 1 , Zhiteng Wang 1 , Lei Lang 1 , Yingguo Yang 2 , Kui Zhao 1 , Shengzhong Frank Liu 1, 3, 4
Affiliation
The critical requirement for ambient-printed formamidinium lead iodide (FAPbI3) lies in the control of nucleation–growth kinetics and defect formation behavior, which are extensively influenced by interactions between the solvent and perovskite. Here, a strategy is developed that combines a cosolvent and an additive to efficiently tailor the coordination between the solvent and perovskite. Through in situ characterizations, the direct crystallization from the sol–gel phase to α-FAPbI3 is illustrated. When the solvent exhibits strong interactions with the perovskite, the sol–gel phases cannot effectively transform into α-FAPbI3, resulting in a lower nucleation rate and confined crystal growth directions. Consequently, it becomes challenging to fabricate high-quality void-free perovskite films. Conversely, weaker solvent–perovskite coordination promotes direct crystallization from sol–gel phases to α-FAPbI3. This process exhibits more balanced nucleation–growth kinetics and restrains the formation of defects and microstrains in situ. This strategy leads to improved structural and optoelectronic properties within the FAPbI3 films, characterized by more compact grain stacking, smoother surface morphology, released lattice strain, and fewer defects. The ambient-printed FAPbI3 perovskite solar cells fabricated using this strategy exhibit a remarkable power conversion efficiency of 24%, with significantly reduced efficiency deviation and negligible decreases in the stabilized output.
中文翻译:
基于溶剂-钙钛矿配位调节的高性能常温可印刷 FAPbI3 钙钛矿太阳能电池的结晶控制
环境印刷甲脒碘化铅(FAPbI 3 )的关键要求在于控制成核-生长动力学和缺陷形成行为,这些行为受到溶剂和钙钛矿之间相互作用的广泛影响。在这里,开发了一种策略,将共溶剂和添加剂结合起来,以有效地调整溶剂和钙钛矿之间的配位。通过原位表征,说明了从溶胶-凝胶相到α-FAPbI 3的直接结晶。当溶剂与钙钛矿表现出强烈的相互作用时,溶胶-凝胶相不能有效地转化为α-FAPbI 3 ,导致较低的成核速率和受限的晶体生长方向。因此,制造高质量的无空隙钙钛矿薄膜变得具有挑战性。相反,较弱的溶剂-钙钛矿配位促进从溶胶-凝胶相直接结晶为α-FAPbI 3 。该过程表现出更平衡的成核-生长动力学,并抑制原位缺陷和微应变的形成。这种策略改善了 FAPbI 3薄膜的结构和光电性能,其特点是晶粒堆积更紧密、表面形态更光滑、晶格应变释放和缺陷更少。使用这种策略制造的常温印刷的 FAPbI 3钙钛矿太阳能电池表现出高达 24% 的显着功率转换效率,效率偏差显着降低,稳定输出的下降可以忽略不计。
更新日期:2023-10-12
中文翻译:
基于溶剂-钙钛矿配位调节的高性能常温可印刷 FAPbI3 钙钛矿太阳能电池的结晶控制
环境印刷甲脒碘化铅(FAPbI 3 )的关键要求在于控制成核-生长动力学和缺陷形成行为,这些行为受到溶剂和钙钛矿之间相互作用的广泛影响。在这里,开发了一种策略,将共溶剂和添加剂结合起来,以有效地调整溶剂和钙钛矿之间的配位。通过原位表征,说明了从溶胶-凝胶相到α-FAPbI 3的直接结晶。当溶剂与钙钛矿表现出强烈的相互作用时,溶胶-凝胶相不能有效地转化为α-FAPbI 3 ,导致较低的成核速率和受限的晶体生长方向。因此,制造高质量的无空隙钙钛矿薄膜变得具有挑战性。相反,较弱的溶剂-钙钛矿配位促进从溶胶-凝胶相直接结晶为α-FAPbI 3 。该过程表现出更平衡的成核-生长动力学,并抑制原位缺陷和微应变的形成。这种策略改善了 FAPbI 3薄膜的结构和光电性能,其特点是晶粒堆积更紧密、表面形态更光滑、晶格应变释放和缺陷更少。使用这种策略制造的常温印刷的 FAPbI 3钙钛矿太阳能电池表现出高达 24% 的显着功率转换效率,效率偏差显着降低,稳定输出的下降可以忽略不计。