journal article·2024-11-07

Transient Exciton-Charge Interconversion in Single-Crystal Hybrid Perovskites

Yulan Fu, Yiwei Zhang, Xinping Zhang

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Abstract

Ultrafast oscillatory transient absorption (TA) dynamics are observed in single crystals of hybrid organic-inorganic perovskite (CH3NH3)PbX3 with X = I, Br, Cl. High-density photoinduced charges, low binding energy of the excitons, efficient generation and high mobility of charges, and long diffusion length of both excitons and charges led to transient interconversion between excitons and charges with high efficiency, which is responsible for the oscillatory TA dynamics at re-excitation by the probe pulses. The pump pulses initiated a quasi-equilibrium scheme of coexisting excitons and charges with high densities, the probe pulse triggered a perturbation through interconversion between these two kinds of excited "particles," which was overlapped on the intrinsic exciton relaxation dynamics, producing an oscillatory modulation with time delay. This not only reveals important photoelectronic processes with determined time scales, but also supplies physics for applications of this group of materials.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · Chalcogenide Semiconductor Thin Films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Information Photonics Technology, School of Physics and Optoelectronic Engineering, Beijing University of Technology, Beijing 100124, P. R. China

Funding

National Natural Science Foundation of China · Beijing Key Lab of Microstructure and Property of Advanced Materials, Beijing University of Technology

References (39)

Show source-provided references
1. 10.1002/adma.20150004810.1002/adma.201500048 ↗
2. 10.1038/srep0772510.1038/srep07725 ↗
3. 10.1126/science.aaa533310.1126/science.aaa5333 ↗
4. 10.1038/ncomms640410.1038/ncomms6404 ↗
5. 10.1002/adma.20140504410.1002/adma.201405044 ↗
6. 10.1038/nnano.2015.9010.1038/nnano.2015.90 ↗
7. 10.1038/ncomms770010.1038/ncomms7700 ↗
8. 10.1039/C4CC07518H10.1039/C4CC07518H ↗
9. 10.1002/adma.20140521710.1002/adma.201405217 ↗
10. 10.1038/nmat427110.1038/nmat4271 ↗
11. 10.1126/science.aan230110.1126/science.aan2301 ↗
12. 10.1126/science.aam565510.1126/science.aam5655 ↗
13. 10.1038/nmat479510.1038/nmat4795 ↗
14. 10.1126/science.aai908110.1126/science.aai9081 ↗
15. 10.1126/science.aao556110.1126/science.aao5561 ↗
16. 10.1021/jz500528510.1021/jz5005285 ↗
17. 10.1038/ncomms458610.1038/ncomms4586 ↗
18. 10.1038/ncomms604910.1038/ncomms6049 ↗
19. 10.1038/nphoton.2014.17110.1038/nphoton.2014.171 ↗
20. 10.1002/adfm.20140442110.1002/adfm.201404421 ↗
21. 10.1038/nphoton.2015.15110.1038/nphoton.2015.151 ↗
22. 10.1021/acs.chemrev.6b0013610.1021/acs.chemrev.6b00136 ↗
23. 10.1021/acsami.6b0577010.1021/acsami.6b05770 ↗
24. 10.1021/acs.jpclett.0c0242510.1021/acs.jpclett.0c02425 ↗
25. 10.1063/5.000860810.1063/5.0008608 ↗
26. 10.1126/science.aaa272510.1126/science.aaa2725 ↗
27. 10.1126/science.aaa576010.1126/science.aaa5760 ↗
28. 10.1038/s41467-017-02039-510.1038/s41467-017-02039-5 ↗
29. 10.1038/nmat476510.1038/nmat4765 ↗
30. 10.1002/ange.20160488010.1002/ange.201604880 ↗
31. 10.1039/C6CE00375C10.1039/C6CE00375C ↗
32. 10.1021/acsnano.1c0911910.1021/acsnano.1c09119 ↗
33. 10.1021/acs.jpclett.0c0256010.1021/acs.jpclett.0c02560 ↗
34. 10.1038/s41377-023-01107-410.1038/s41377-023-01107-4 ↗
35. 10.1021/jp407065h10.1021/jp407065h ↗
36. 10.1103/PhysRevLett.83.441710.1103/PhysRevLett.83.4417 ↗
37. 10.1103/PhysRevB.75.24512810.1103/PhysRevB.75.245128 ↗
38. 10.1103/PhysRevB.73.24520110.1103/PhysRevB.73.245201 ↗
39. 10.1080/0950034080240989210.1080/09500340802409892 ↗