Semiconducting Organic–Inorganic Hybrid Material with Distinct Switchable Dielectric Phase Transition
Source abstract
Abstract
Hybrid materials such as CH 3 NH 3 PbI 3 have led to significant attention because of their great properties and promising potential applications in photovoltaic, optoelectronic devices, and sensing. However, there is a huge challenge to realize the dielectric switching/ferroelectricity and semiconducting attribute for these materials simultaneously. Modifying the halogen/metal and even controlling the dimensionality of the inorganic framework provide the possibility to obtain new or high-performance functional materials. Here, we designed a hybrid compound, [(CH 3 ) 3 NOH] 2 BiCl 5, which shows remarkable dielectric switching properties at T c = 183.5 K and semiconducting behavior with an optical band gap of ∼3.225 eV. Experimental analysis revealed that the synergistic effect of microstructure of organic cations and inorganic frameworks contributes to the multifeatured. The implementation of switching and semiconducting properties in the material has essential significance for expanding research on hybrid materials and the development of dielectric-optoelectronic integration devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · Nonlinear Optical Materials Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Ordered Matter Science Research Center, Jiangsu Key Laboratory for Science and Applications of Molecular Ferroelectrics, Southeast University, Nanjing 211189, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Southeast University
References (44)
Show source-provided references
1. 10.1038/natrevmats.2016.9910.1038/natrevmats.2016.99 ↗
2. 10.1021/ja809598r10.1021/ja809598r ↗
3. 10.1002/adma.20160299210.1002/adma.201602992 ↗
4. 10.1038/ncomms1405110.1038/ncomms14051 ↗
5. 10.1126/science.124398210.1126/science.1243982 ↗
6. 10.1126/science.122860410.1126/science.1228604 ↗
7. 10.1002/anie.20130871910.1002/anie.201308719 ↗
8. 10.1021/ja412583t10.1021/ja412583t ↗
9. 10.1038/am.2016.19310.1038/am.2016.193 ↗
10. 10.1039/b817891g10.1039/b817891g ↗
11. 10.1002/adma.20150522410.1002/adma.201505224 ↗
12. 10.1038/ncomms690010.1038/ncomms6900 ↗
13. 10.1002/anie.20160607910.1002/anie.201606079 ↗
14. 10.1039/c7tc00279c10.1039/c7tc00279c ↗
15. 10.1039/c5tc03683f10.1039/c5tc03683f ↗
16. 10.1002/adma.20160089510.1002/adma.201600895 ↗
17. 10.1002/anie.20060220510.1002/anie.200602205 ↗
18. 10.1021/cm980321y10.1021/cm980321y ↗
19. 10.1002/advs.20150002910.1002/advs.201500029 ↗
20. 10.1039/c8tc00419f10.1039/c8tc00419f ↗
21. 10.1021/jacs.7b1252410.1021/jacs.7b12524 ↗
22. 10.1021/cr980073p10.1021/cr980073p ↗
23. 10.1103/physrevapplied.6.02100110.1103/physrevapplied.6.021001 ↗
24. 10.1021/cr990022810.1021/cr9900228 ↗
25. 10.1002/anie.20100120810.1002/anie.201001208 ↗
26. 10.1039/c5cs00308c10.1039/c5cs00308c ↗
27. 10.1039/c6ce01485b10.1039/c6ce01485b ↗
28. 10.1039/c7qi00722a10.1039/c7qi00722a ↗
29. 10.1021/acs.chemrev.5b0071510.1021/acs.chemrev.5b00715 ↗
30. 10.1039/c7dt03622a10.1039/c7dt03622a ↗
31. 10.1039/c7qi00301c10.1039/c7qi00301c ↗
32. 10.1021/jacs.8b0401410.1021/jacs.8b04014 ↗
33. 10.1002/anie.20180371610.1002/anie.201803716 ↗
34. 10.1002/anie.20170958810.1002/anie.201709588 ↗
35. 10.1002/ange.1963075140210.1002/ange.19630751402 ↗
36. 10.1002/pssb.1966015022410.1002/pssb.19660150224 ↗
37. 10.1016/j.mee.2005.03.05510.1016/j.mee.2005.03.055 ↗
38. 10.1103/physrevb.36.649710.1103/physrevb.36.6497 ↗
39. 10.1021/ja311033510.1021/ja3110335 ↗
40. 10.1039/b819473d10.1039/b819473d ↗
41. 10.1021/acs.jpcc.7b0512610.1021/acs.jpcc.7b05126 ↗
42. 10.1107/s056773947600155110.1107/s0567739476001551 ↗
43. 10.1103/physrevlett.103.02680110.1103/physrevlett.103.026801 ↗
44. 10.13031/2013.1714210.13031/2013.17142 ↗