Vicente Juvinch R, Chen Jixin
Department of Chemistry, University of the Philippines Visayas, Miagao, Iloilo 5023, Philippines.
J Phys Chem Lett. 2020 Mar 5;11(5):1802-1807. doi: 10.1021/acs.jpclett.9b03734. Epub 2020 Feb 20.
Mixed-halide lead perovskites (MHPs) are promising materials for photovoltaics and optoelectronics due to their highly tunable band gaps. However, they phase segregate under continuous illumination or an electric field, the mechanism of which is still under debate. Herein we systematically measure the phase segregation behavior of polymer-encapsulated CHNHPb(BrI) MHPs as a function of excitation intensity and the nominal halide ratio by in situ photoluminescence microspectroscopy and observe surprising phase dynamics at the beginning of the illumination. The initial phase segregation to I-rich and Br-rich phases is observed followed by the formation of a new mixed-halide phase within several seconds that has not been reported before. We propose that the photothermal effect is amplified at the small-size I-rich domains, which significantly changes the local phase segregation in the otherwise uniform film within milliseconds after illumination.
混合卤化物铅基钙钛矿(MHP)因其具有高度可调的带隙,是用于光伏和光电子学的有前途的材料。然而,它们在持续光照或电场下会发生相分离,其机制仍在争论中。在此,我们通过原位光致发光显微光谱系统地测量了聚合物封装的CHNHPb(BrI) MHP的相分离行为,该行为是激发强度和名义卤化物比率的函数,并在光照开始时观察到了惊人的相动力学。观察到最初向富碘相和富溴相的相分离,随后在几秒钟内形成了一个以前未报道过的新的混合卤化物相。我们提出,光热效应在小尺寸的富碘区域被放大,这在光照后几毫秒内显著改变了原本均匀薄膜中的局部相分离。