Potassium Ion Assisted Synthesis of Organic–Inorganic Hybrid Perovskite Nanobelts for Stable and Flexible Photodetectors
Source abstract
Abstract
Abstract Low‐dimensional organic–inorganic hybrid perovskites with controllable morphologies are attractive for high‐performance optoelectronic devices. In particular, the 1D organic–inorganic hybrid perovskite nanowires/nanobelts are promising for flexible photodetectors due to high photoresponsivity and strain endurance capability. Herein, a novel and large‐scale synthesis of (C4H9NH3)2PbBr4 organic–inorganic hybrid perovskite nanobelt achieved by the potassium ions assisted controllable crystal growth during the precipitation process in solutions is reported. The obtained (C4H9NH3)2PbBr4 perovskite nanobelts exhibit high‐efficient photoluminescence and superior stability under ambient conditions. Furthermore, these nanobelts are used as photoresponsive materials to fabricate flexible photodetectors, which show much higher switching ratio than that of photodetectors based on (C4H9NH3)2PbBr4 microplatelets. Attractively, after repeated bending for 1000 times, the nanobelt‐based photodetector only shows less than 10% decay in switching ratio in contrast to at least 40% of switching ratio decay for the microplatelets‐based photodetector. The reported potassium ion assisted large‐scale synthesis of (C4H9NH3)2PbBr4 nanobelts paves a new avenue for the application of organic–inorganic hybrid perovskites in flexible optoelectronic devices.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · 2D Materials and Applications · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Division of Nanomaterials & Chemistry Hefei National Laboratory for Physical Sciences at the Microscale Department of Chemistry CAS Center for Excellence in Nanoscience Hefei Science Center of CAS Collaborative Innovation Center of Suzhou Nano Science and Technology University of Science and Technology of China 96 Jinzhai Road Hefei Anhui 230026 China
Funding
National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1038/nnano.2014.14910.1038/nnano.2014.149 ↗
2. 10.1002/anie.20170113410.1002/anie.201701134 ↗
3. 10.1021/acsami.6b0948910.1021/acsami.6b09489 ↗
4. 10.1038/nnano.2015.9010.1038/nnano.2015.90 ↗
5. 10.1038/ncomms838310.1038/ncomms8383 ↗
6. 10.1002/adma.20150395410.1002/adma.201503954 ↗
7. 10.1038/ncomms640410.1038/ncomms6404 ↗
8. 10.1002/adma.20160026510.1002/adma.201600265 ↗
9. 10.1038/nphoton.2014.13410.1038/nphoton.2014.134 ↗
10. 10.1021/ic401215x10.1021/ic401215x ↗
11. 10.1039/C6SC04474C10.1039/C6SC04474C ↗
12. 10.1021/acs.chemmater.6b0179310.1021/acs.chemmater.6b01793 ↗
13. 10.1021/acs.chemmater.6b0396510.1021/acs.chemmater.6b03965 ↗
14. 10.1021/acs.nanolett.5b0405310.1021/acs.nanolett.5b04053 ↗
15. 10.1021/acsnano.6b0268310.1021/acsnano.6b02683 ↗
16. 10.1038/ncomms1405110.1038/ncomms14051 ↗
17. 10.1021/acs.nanolett.7b0016610.1021/acs.nanolett.7b00166 ↗
18. 10.1002/anie.20141195610.1002/anie.201411956 ↗
19. 10.1002/anie.20140646610.1002/anie.201406466 ↗
20. 10.1021/jacs.5b1174010.1021/jacs.5b11740 ↗
21. 10.1126/science.aac766010.1126/science.aac7660 ↗
22. 10.1002/anie.20161179410.1002/anie.201611794 ↗
23. 10.1021/jacs.6b1168310.1021/jacs.6b11683 ↗
24. 10.1021/acsenergylett.6b0070510.1021/acsenergylett.6b00705 ↗
25. 10.1002/aenm.20160173110.1002/aenm.201601731 ↗
26. 10.1002/adma.20160066910.1002/adma.201600669 ↗
27. 10.1038/nenergy.2016.19410.1038/nenergy.2016.194 ↗
28. 10.1039/b110309a10.1039/b110309a ↗
29. 10.1016/j.jallcom.2009.01.00110.1016/j.jallcom.2009.01.001 ↗
30. 10.1366/000370289420293110.1366/0003702894202931 ↗
31. 10.1002/adma.20160078410.1002/adma.201600784 ↗
32. 10.1021/acsnano.6b0386310.1021/acsnano.6b03863 ↗
33. 10.1063/1.479266710.1063/1.4792667 ↗
34. 10.1021/jacs.6b1022710.1021/jacs.6b10227 ↗
35. 10.1002/adma.20160022510.1002/adma.201600225 ↗
36. 10.1021/ja910871s10.1021/ja910871s ↗
37. 10.1002/adma.20160046810.1002/adma.201600468 ↗