Abstract
The presence of the heavy elements leads to strong spin-orbit coupling (SOC) in hybrid organic-inorganic perovskites (HOIPs), which plays an important role in the photovoltaic performance of HOIPs by changing the populations between bright and dark states. The organic cation is a critical composition and affects SOC via the interaction with the inorganic cage. In this work, we use magneto-photocurrent measurement to explore the SOC effect upon using mixed organic cations (methylammonium (MA) and formamidinium (FA)) with different dipole moments in Pb based perovskites. Magneto-photocurrent measurements showed that the internal magnetic parameter B0 is decreased from 402.41 mT to 180.18 mT and 104.58 mT with decreasing the MA/FA ratio. This provides evidence that changing the internal dipole moment by using mixed organic cations can essentially change the SOC in HOIPs. Simultaneously, the photocurrent is increased from 21.46 mA/cm2 to 22.60 mA/cm2 and 23.08 mA/cm2 when the MA/FA ratio is changed from 1:0 to 0.9:0.1 and 0.7:0.3. Above all, our results indicate that the change in SOC by different organic cations can also be a factor affecting the performance of perovskite solar cells.
Original language | English |
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Article number | 105671 |
Journal | Organic Electronics |
Volume | 81 |
DOIs | |
State | Published - Jun 2020 |
Externally published | Yes |
Funding
This research was supported by the financial supports from Air Force Office of Scientific Research (AFOSR) under the grant number FA 9550-15-1-0064 , AOARD ( FA2386-15-1-4104 ), and National Science Foundation ( NSF-1911659 ). This research was partially conducted at the Center for Nanophase Materials Sciences based on user projects (CNMS2016-279, CNMS2016-R45, CNMS-2019-057), which is a U.S. Department of Energy Office of Science User Facility . The author (Y-X Dou) acknowledges the financial support from the China Scholarship Council through university agreement for her Ph.D study at the University of Tennessee (Knoxville). This research was supported by the financial supports from Air Force Office of Scientific Research (AFOSR) under the grant number FA 9550-15-1-0064, AOARD (FA2386-15-1-4104), and National Science Foundation (NSF-1911659). This research was partially conducted at the Center for Nanophase Materials Sciences based on user projects (CNMS2016-279, CNMS2016-R45, CNMS-2019-057), which is a U.S. Department of Energy Office of Science User Facility. The author (Y-X Dou) acknowledges the financial support from the China Scholarship Council through university agreement for her Ph.D study at the University of Tennessee (Knoxville).
Funders | Funder number |
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National Science Foundation | CNMS-2019-057, 1911659, CNMS2016-279, NSF-1911659, CNMS2016-R45 |
U.S. Department of Energy | |
Air Force Office of Scientific Research | FA2386-15-1-4104, FA 9550-15-1-0064 |
University of Tennessee | |
China Scholarship Council |
Keywords
- Organic cation
- Perovskites
- Photocurrent
- Solar cells
- Spin-orbit coupling