Abstract
Hybrid perovskites, as emerging multifunctional semiconductors, have demonstrated dual electronic/ionic conduction properties. We report a metal/ion interaction induced p-i-n junction across slightly n-type doped MAPbI3 single crystals with Au/MAPbI3/Ag configuration based on interface dependent Seebeck effect, Hall effect and time-of-flight secondary ion mass spectrometry analysis. The organic cations (MA+) interact with Au atoms, forming positively charged coordination complexes at Au/MAPbI3 interface, whereas iodine anions (I-) can react with Ag contacts, leading to interfacial ionic polarization. Such metal/ion interactions establish a p-doped region near the Au/MAPbI3 interface due to the formation of MA+ vacancies, and an n-doped region near the Ag/MAPbI3 interface due to formation of I- vacancies, consequently forming a p-i-n junction across the crystal in Au/MAPbI3/Ag configuration. Therefore, the metal/ion interaction plays a role in determining the surface electronic structure and semiconducting properties of hybrid perovskites.
Original language | English |
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Pages (from-to) | 17285-17288 |
Number of pages | 4 |
Journal | Journal of the American Chemical Society |
Volume | 139 |
Issue number | 48 |
DOIs | |
State | Published - Dec 6 2017 |
Funding
This research is supported by the Air Force Office of Scientific Research (FA 9550-15-1-0064) and the National Science Foundation (CBET-1438181). This research was partially conducted at the Center for Nanophase Materials Sciences (based on Projects (CNMS2016-279 and CNMS2016-R45), which is sponsored at Oak Ridge National Laboratory by the Division of Scientific User Facilities, U.S. Department of Energy. B.H. acknowledges project support from the National Natural Science Foundation of China (21161160445 and 61077020). R.M. and D.M. acknowledge support from the Gordon and Betty Moore Foundation's EPiQS Initiative (GBMF4416). This research is supported by the Air Force Office of Scientific Research (FA 9550-15-1-0064) and the National Science Foundation (CBET-1438181). This research was partially conducted at the Center for Nanophase Materials Sciences (based on Projects (CNMS2016-279 and CNMS2016-R45), which is sponsored at Oak Ridge National Laboratory by the Division of Scientific User Facilities, U.S. Department of Energy. B.H. acknowledges project support from the National Natural Science Foundation of China (21161160445 and 61077020). R.M. and D.M. acknowledge support from the Gordon and Betty Moore Foundation’s EPiQS Initiative (GBMF4416).
Funders | Funder number |
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Air Force Office of Scientific Research | |
Center for Nanophase Materials Sciences | CNMS2016-279, CNMS2016-R45 |
National Natural Science Foundation of China | |
National Science Foundation | |
National Science Foundation | CBET-1438181 |
U.S. Department of Energy | |
Air Force Office of Scientific Research | FA 9550-15-1-0064 |
Gordon and Betty Moore Foundation | GBMF4416 |
Basic Energy Sciences | |
Oak Ridge National Laboratory | |
National Natural Science Foundation of China | 61077020, 21161160445 |