Iodomethane-Mediated Organometal Halide Perovskite with Record Photoluminescence Lifetime
Iodomethane-Mediated Organometal Halide Perovskite with Record Photoluminescence Lifetime
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碘甲烷介导的有机金属卤化物钙钛矿具有创纪录的光致发光寿命
DOI:
10.1021/acsami.6b05770
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发表时间:
2016
影响因子:
9.5
通讯作者:
Sun Baoquan
中科院分区:
文献类型:
--
作者:
Xu Weidong;McLeod John A.;Yang Yingguo;Wang Yimeng;Wu Zhongwei;Bai Sai;Yuan Zhongcheng;Song Tao;Wang Yusheng;Si Junjie;Wang Rongbin;Gao Xingyu;Zhang Xinping;Liu Lijia;Sun Baoquan
Organometallic lead halide perovskites are excellent light harvesters for high-efficiency photovoltaic devices. However, as the key component in these devices, a perovskite thin film with good morphology and minimal trap states is still difficult to obtain. Herein we show that by incorporating a low boiling point alkyl halide such as iodomethane (CH3I) into the precursor solution, a perovskite (CH3NH3PbI3–xClx) film with improved grain size and orientation can be easily achieved. More importantly, these films exhibit a significantly reduced amount of trap states. Record photoluminescence lifetimes of more than 4 μs are achieved; these lifetimes are significantly longer than that of pristine CH3NH3PbI3–xClxfilms. Planar heterojunction solar cells incorporating these CH3I-mediated perovskites have demonstrated a dramatically increased power conversion efficiency compared to the ones using pristine CH3NH3PbI3–xClx. Photoluminescence, transient absorption, and microwave detected photoconductivity measurements all provide consistent evidence that CH3I addition increases the number of excitons generated and their diffusion length, both of which assist efficient carrier transport in the photovoltaic device. The simple incorporation of alkyl halide to enhance perovskite surface passivation introduces an important direction for future progress on high efficiency perovskite optoelectronic devices.