Department of Physics, University of Texas at Austin, Austin, TX, 78712, USA.
National Renewable Energy Laboratory, Golden, CO, 80401, USA.
Nat Commun. 2017 Dec 20;8(1):2230. doi: 10.1038/s41467-017-02331-4.
Organic-inorganic perovskite solar cells have attracted tremendous attention because of their remarkably high power conversion efficiencies. To further improve device performance, it is imperative to obtain fundamental understandings on the photo-response and long-term stability down to the microscopic level. Here, we report the quantitative nanoscale photoconductivity imaging on two methylammonium lead triiodide thin films with different efficiencies by light-stimulated microwave impedance microscopy. The microwave signals are largely uniform across grains and grain boundaries, suggesting that microstructures do not lead to strong spatial variations of the intrinsic photo-response. In contrast, the measured photoconductivity and lifetime are strongly affected by bulk properties such as the sample crystallinity. As visualized by the spatial evolution of local photoconductivity, the degradation process begins with the disintegration of grains rather than nucleation and propagation from visible boundaries between grains. Our findings provide insights to improve the electro-optical properties of perovskite thin films towards large-scale commercialization.
有机-无机钙钛矿太阳能电池因其极高的功率转换效率而受到极大关注。为了进一步提高器件性能,必须从微观层面获得对光响应和长期稳定性的基本理解。在这里,我们通过受激发射微波阻抗显微镜报告了对两个效率不同的甲脒碘化铅薄膜的定量纳米级光电导成像。微波信号在晶粒和晶界上都非常均匀,这表明微结构不会导致固有光响应的强烈空间变化。相比之下,所测量的光电导和寿命强烈受到样品结晶度等体相性质的影响。通过局部光电导的空间演化,可见降解过程始于晶粒的解体,而不是从晶粒之间可见边界的成核和扩展开始。我们的研究结果为改善钙钛矿薄膜的光电性能以实现大规模商业化提供了思路。