Yanagida Masatoshi, Shirai Yasuhiro, Khadka Dhruba B, Miyano Kenjiro
Centre for Green Research on Energy and Environmental Materials, National Institute for Materials Science (NIMS) 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Phys Chem Chem Phys. 2020 Nov 21;22(43):25118-25125. doi: 10.1039/d0cp04350h. Epub 2020 Oct 29.
We use photoinduced absorption spectroscopy (PAS) to study the ionic motion in CHNHPbI perovskite solar cells, consisting of indium tin oxide (ITO)/NiOx/perovskite/phenyl-C-butyric-acid-methyl ester (PCBM)/aluminum-doped zinc oxide (AZO)/ITO. We observed a slow (∼50 mHz) spectral blue shift (∼10 eV) under modulated 520 nm illumination, which we interpreted in terms of the modulation in the bulk ion density. Numerical simulation shows that the mobile ion moves in and out from the double layers at the perovskite/charge transport layer interfaces in order to recover the bulk charge neutrality tipped off-balance by the photocarriers. The diffusion coefficient of the ion is 10 to 10 cm s, when we assume that the characteristic time constant of the ion motion is governed by the diffusion.
我们使用光致吸收光谱(PAS)来研究CHNHPbI钙钛矿太阳能电池中的离子运动,该电池由氧化铟锡(ITO)/氧化镍(NiOx)/钙钛矿/苯基-C-丁酸甲酯(PCBM)/铝掺杂氧化锌(AZO)/ITO组成。我们观察到在调制的520 nm光照下,光谱出现缓慢(约50 mHz)的蓝移(约10 eV),我们将其解释为体离子密度的调制。数值模拟表明,移动离子在钙钛矿/电荷传输层界面的双层中进出移动,以恢复因光载流子而失衡的体电荷中性。当我们假设离子运动的特征时间常数由扩散控制时,离子的扩散系数为10至10 cm²/s。