TY - JOUR
T1 - A fabrication process for flexible single-crystal perovskite devices
AU - Lei, Yusheng
AU - Chen, Yimu
AU - Zhang, Ruiqi
AU - Li, Yuheng
AU - Yan, Qizhang
AU - Lee, Seunghyun
AU - Yu, Yugang
AU - Tsai, Hsinhan
AU - Choi, Woojin
AU - Wang, Kaiping
AU - Luo, Yanqi
AU - Gu, Yue
AU - Zheng, Xinran
AU - Wang, Chunfeng
AU - Wang, Chonghe
AU - Hu, Hongjie
AU - Li, Yang
AU - Qi, Baiyan
AU - Lin, Muyang
AU - Zhang, Zhuorui
AU - Dayeh, Shadi A.
AU - Pharr, Matt
AU - Fenning, David P.
AU - Lo, Yu Hwa
AU - Luo, Jian
AU - Yang, Kesong
AU - Yoo, Jinkyoung
AU - Nie, Wanyi
AU - Xu, Sheng
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/7/30
Y1 - 2020/7/30
N2 - Organic–inorganic hybrid perovskites have electronic and optoelectronic properties that make them appealing in many device applications1–4. Although many approaches focus on polycrystalline materials5–7, single-crystal hybrid perovskites show improved carrier transport and enhanced stability over their polycrystalline counterparts, due to their orientation-dependent transport behaviour8–10 and lower defect concentrations11,12. However, the fabrication of single-crystal hybrid perovskites, and controlling their morphology and composition, are challenging12. Here we report a solution-based lithography-assisted epitaxial-growth-and-transfer method for fabricating single-crystal hybrid perovskites on arbitrary substrates, with precise control of their thickness (from about 600 nanometres to about 100 micrometres), area (continuous thin films up to about 5.5 centimetres by 5.5 centimetres), and composition gradient in the thickness direction (for example, from methylammonium lead iodide, MAPbI3, to MAPb0.5Sn0.5I3). The transferred single-crystal hybrid perovskites are of comparable quality to those directly grown on epitaxial substrates, and are mechanically flexible depending on the thickness. Lead–tin gradient alloying allows the formation of a graded electronic bandgap, which increases the carrier mobility and impedes carrier recombination. Devices based on these single-crystal hybrid perovskites show not only high stability against various degradation factors but also good performance (for example, solar cells based on lead–tin-gradient structures with an average efficiency of 18.77 per cent).
AB - Organic–inorganic hybrid perovskites have electronic and optoelectronic properties that make them appealing in many device applications1–4. Although many approaches focus on polycrystalline materials5–7, single-crystal hybrid perovskites show improved carrier transport and enhanced stability over their polycrystalline counterparts, due to their orientation-dependent transport behaviour8–10 and lower defect concentrations11,12. However, the fabrication of single-crystal hybrid perovskites, and controlling their morphology and composition, are challenging12. Here we report a solution-based lithography-assisted epitaxial-growth-and-transfer method for fabricating single-crystal hybrid perovskites on arbitrary substrates, with precise control of their thickness (from about 600 nanometres to about 100 micrometres), area (continuous thin films up to about 5.5 centimetres by 5.5 centimetres), and composition gradient in the thickness direction (for example, from methylammonium lead iodide, MAPbI3, to MAPb0.5Sn0.5I3). The transferred single-crystal hybrid perovskites are of comparable quality to those directly grown on epitaxial substrates, and are mechanically flexible depending on the thickness. Lead–tin gradient alloying allows the formation of a graded electronic bandgap, which increases the carrier mobility and impedes carrier recombination. Devices based on these single-crystal hybrid perovskites show not only high stability against various degradation factors but also good performance (for example, solar cells based on lead–tin-gradient structures with an average efficiency of 18.77 per cent).
UR - https://www.scopus.com/pages/publications/85088804969
U2 - 10.1038/s41586-020-2526-z
DO - 10.1038/s41586-020-2526-z
M3 - Article
C2 - 32728239
AN - SCOPUS:85088804969
SN - 0028-0836
VL - 583
SP - 790
EP - 795
JO - Nature
JF - Nature
IS - 7818
ER -