自愈
弹性(材料科学)
光降解
动力学
光伏
材料科学
纳米技术
化学
化学工程
光催化
光伏系统
复合材料
有机化学
催化作用
物理
病理
工程类
生物
替代医学
医学
量子力学
生态学
作者
Pallavi Singh,Davide Raffaele Ceratti,Yahel Soffer,Sudipta Bera,Yishay Feldman,Michael Elbaum,Dan Oron,David Cahen,Gary Hodes
标识
DOI:10.1021/acs.jpcc.4c06090
摘要
Self-healing materials can become game changers for developing sustainable (opto)electronics. APbX3 halide (=X-) perovskites, HaPs, have shown a remarkable ability to self-heal damage. While we demonstrated self-healing in pure HaP compounds, in single crystals, and in polycrystalline thin films (as used in most devices), HaP compositions with multiple A+ (and X-) constituents are preferred for solar cells. We now show self-healing in mixed A+ HaPs. Specifically, if at least 15 atom % of the methylammonium (MA+) A cation is substituted for by guanidinium (Gua+) or acetamidinium (AA+), then the self-healing rate after damage is enhanced. In contrast, replacing MA+ with dimethylammonium (DMA+), comparable in size to Gua+ or AA+, does not alter this rate. Based on the times for self-healing, we infer that the rate-determining step involves short-range diffusion of A+ and/or Pb2+ cations and that the self-healing rate correlates with the strain in the material, the A+ cation dipole moment, and H-bonding between A+ and I-. These insights may offer clues for developing a detailed self-healing mechanism and understanding the kinetics to guide the design of self-healing materials. Fast recovery kinetics are important from the device perspective, as they allow complete recovery in devices during operation or when switched off (LEDs)/in the dark (photovoltaics).
科研通智能强力驱动
Strongly Powered by AbleSci AI