journal article·2018-10

Enhancement of Stability and Photocatalytic Performance on Hybrid Perovskite with Aniline

Yidi Wang, Liangfeng Luo, Lei Chen, Pui Fai Ng, Ka I Lee, Bin Fei

ChemNanoMat· Volume 4· Issue 10
Publisher page

Abstract

Abstract Aniline was introduced into the synthesis of methylammonium lead bromide MAPbBr3 (M‐PE) as a capping ligand. With the appropriate steric hindrance, aniline effectively bound to the surface of M‐PE particles and exposed hydrophobic phenyl groups, which were greatly beneficial for the enhancement of stability. M‐PE and aniline‐capped M‐PE (AM‐PE) were characterized by XRD, photoluminescence, UV/Vis spectroscopy, SEM and TEM. AM‐PE showed more uniform morphology and much higher stability in polar solvents. AM‐PE was almost unchanged in acetone within 100 hours while M‐PE completely decomposed within 24 hours. Light harvesting in the visible region was also enhanced by aniline, so that AM‐PE had much better performance for photodegradation of malachite green (MaG) than M‐PE. In addition, the decomposition process of M‐PE and AM‐PE was also investigated in detail.
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Research context

OpenAlex topics: Perovskite Materials and Applications · Advanced Photocatalysis Techniques · Conducting polymers and applications

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

Affiliations

Institute of Textiles and Clothing Hong Kong Polytechnic University Hong Kong China.

Funding

Hong Kong Polytechnic University

References (48)

Show source-provided references
1.
2. 10.1039/C4EE00942H10.1039/C4EE00942H ↗
3. 10.1038/nmat406510.1038/nmat4065 ↗
4. 10.1021/nl504349z10.1021/nl504349z ↗
5. 10.1038/srep0059110.1038/srep00591 ↗
6. 10.1126/science.aaa927210.1126/science.aaa9272 ↗
7. 10.1126/sciadv.150117010.1126/sciadv.1501170 ↗
8. NREL Efficiency Chart https://www.nrel.gov/pv/assets/images/efficiency-chart.png. (accessed 30 October 2017)
9. 10.1039/C4TA04953E10.1039/C4TA04953E ↗
10. 10.1021/acs.chemmater.5b0376910.1021/acs.chemmater.5b03769 ↗
11.
12. 10.1002/anie.20160223610.1002/anie.201602236 ↗
13. 10.1002/ange.20160223610.1002/ange.201602236 ↗
14. 10.1039/C5TC04116C10.1039/C5TC04116C ↗
15. 10.1039/c3ta10518k10.1039/c3ta10518k ↗
16.
17. 10.1038/ncomms1173510.1038/ncomms11735 ↗
18. 10.1039/C6EE02013E10.1039/C6EE02013E ↗
19. 10.1038/nphoton.2016.18510.1038/nphoton.2016.185 ↗
20.
21. 10.1021/acs.chemmater.7b0350410.1021/acs.chemmater.7b03504 ↗
22. Sun S. B. · ACS Nano
23. 10.1021/ja500628810.1021/ja5006288 ↗
24. 10.1021/acsnano.5b0115410.1021/acsnano.5b01154 ↗
25. 10.1021/acs.jpclett.7b0239910.1021/acs.jpclett.7b02399 ↗
26. 10.1038/nmat452610.1038/nmat4526 ↗
27. 10.1021/acs.nanolett.5b0298510.1021/acs.nanolett.5b02985 ↗
28.
29. 10.1021/jacs.5b0379610.1021/jacs.5b03796 ↗
30. 10.1039/C5NR06890H10.1039/C5NR06890H ↗
31. 10.1021/ja410920910.1021/ja4109209 ↗
32. 10.1039/C7TA08190A10.1039/C7TA08190A ↗
33.
34. 10.1002/ppsc.20140007410.1002/ppsc.201400074 ↗
35. 10.1021/jp109381r10.1021/jp109381r ↗
36. 10.1021/ja203674910.1021/ja2036749 ↗
37. 10.1016/j.cej.2016.06.02210.1016/j.cej.2016.06.022 ↗
38. 10.1039/C3TA13751A10.1039/C3TA13751A ↗
39. 10.1016/j.apcatb.2016.01.00910.1016/j.apcatb.2016.01.009 ↗
40.
41. 10.1002/adma.20150395410.1002/adma.201503954 ↗
42. 10.1021/acs.nanolett.5b0208210.1021/acs.nanolett.5b02082 ↗
43. 10.1021/acs.chemmater.5b0376910.1021/acs.chemmater.5b03769 ↗
44. 10.1039/C5CC09762B10.1039/C5CC09762B ↗
45. 10.1002/smll.20170376210.1002/smll.201703762 ↗
46.
47. 10.1039/C4TA05878J10.1039/C4TA05878J ↗
48. 10.1021/nn507020s10.1021/nn507020s ↗