journal article·2020-06Open access

Aggregation‐induced emission luminogen: A new perspective in the photo‐degradation of organic pollutants

Zhen Hu, Ying Li, Miaomiao Kang, Md. Monarul Islam, Mengsi Chen, Jun Zhang, Ye Xiao, Xing Feng, Carl Redshaw, Menglong Zhang, Qing Chen, Sheng Xie, Jacky W. Y. Lam, Ben Zhong Tang

EcoMat· Volume 2· Issue 2

Abstract

Abstract Both the variety and uniqueness of organic semiconductors has contributed to the rapid development of environmental engineering applications and renewable fuel production, typified by the photodegradation of organic pollutants or water splitting. This paper presents a rare example of an aggregation‐induced emission luminogen as a highly efficient photocatalyst for pollutant decomposition in an environmentally relevant application. Under irradiation, the tetraphenylethene‐based AIEgen ( TPE‐Ca ) exhibited high photo‐degradation efficiency of up to 98.7% of Rhodamine B (RhB) in aqueous solution. The possible photocatalytic mechanism was studied by electron paramagnetic resonance and X‐ray photoelectron spectroscopy spectra, electrochemistry, thermal imaging technology, ultra‐performance liquid chromatography and high‐definition mass spectrometry, as well as by density functional theory calculations. Among the many diverse AIEgens, this is the first AIEgen to be developed as a photocatalyst for the degradation of organic pollutants. This research will open up new avenues for AIEgens research, particularly for applications of environmental relevance. image
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Advanced Photocatalysis Techniques · Molecular Sensors and Ion Detection

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

Affiliations

Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, School of Material and Energy Guangdong University of Technology Guangzhou China

Department of Chemistry, the Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction and Institute for Advanced Study The Hong Kong University of Science and Technology Clear Water Bay Hong Kong China

Department of Chemistry and Biochemistry University of Hull Hull UK

Institute of Semiconductors Materials and Technology South China Normal University Guangzhou China

Beijing Enterprise Water Group Limited Beijing China

Funding

Guangdong University of Technology · National Natural Science Foundation of China

References (80)

Show source-provided references
1. 10.1038/nature0944010.1038/nature09440 ↗
2. 10.1021/es902912310.1021/es9029123 ↗
3. 10.1016/j.watres.2010.02.03910.1016/j.watres.2010.02.039 ↗
4. 10.1016/j.watres.2012.11.02710.1016/j.watres.2012.11.027 ↗
5. 10.1021/acs.chemrev.6b0032710.1021/acs.chemrev.6b00327 ↗
6. 10.1021/cr100454n10.1021/cr100454n ↗
7. 10.1021/cr100164510.1021/cr1001645 ↗
8. 10.1039/C7TA07208B10.1039/C7TA07208B ↗
9. 10.1002/smll.20150355310.1002/smll.201503553 ↗
10. 10.1039/C7TA07509J10.1039/C7TA07509J ↗
11. 10.1021/acs.nanolett.6b0129810.1021/acs.nanolett.6b01298 ↗
12. 10.1002/anie.20150558110.1002/anie.201505581 ↗
13. 10.1016/j.apcatb.2018.03.03910.1016/j.apcatb.2018.03.039 ↗
14. 10.1039/C7CC05444K10.1039/C7CC05444K ↗
15. 10.1039/C6SE00004E10.1039/C6SE00004E ↗
16. 10.1002/adma.20150205710.1002/adma.201502057 ↗
17. 10.1016/j.jorganchem.2017.01.01110.1016/j.jorganchem.2017.01.011 ↗
18. 10.1007/s10904-018-0867-y10.1007/s10904-018-0867-y ↗
19. Polarization charges in a high‐performance GaN/InGaNcore/shell multiple quantum well nanowire for solar energy harvesting10.1109/TNANO.2018.2848287 ↗
20. 10.1039/C8TA03807D10.1039/C8TA03807D ↗
21. 10.1021/jp505783y10.1021/jp505783y ↗
22. 10.1021/acs.est.8b0492310.1021/acs.est.8b04923 ↗
23. 10.1021/acs.iecr.7b0464110.1021/acs.iecr.7b04641 ↗
24. 10.1021/acscatal.6b0222810.1021/acscatal.6b02228 ↗
25. 10.1021/acs.chemrev.5b0060310.1021/acs.chemrev.5b00603 ↗
26. 10.1021/acscatal.8b0352110.1021/acscatal.8b03521 ↗
27. 10.1021/acsenergylett.8b0172210.1021/acsenergylett.8b01722 ↗
28. 10.1021/jz200396h10.1021/jz200396h ↗
29. 10.1039/b105159h10.1039/b105159h ↗
30. 10.1039/c1cs15113d10.1039/c1cs15113d ↗
31. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
32. 10.1038/nrd138510.1038/nrd1385 ↗
33. 10.1039/C9QM00090A10.1039/C9QM00090A ↗
34. 10.1039/C7TA09443D10.1039/C7TA09443D ↗
35. 10.1002/adma.20160619810.1002/adma.201606198 ↗
36. 10.1039/C7CC04864E10.1039/C7CC04864E ↗
37. 10.1021/acsabm.8b0060010.1021/acsabm.8b00600 ↗
38. 10.1039/D0SC00785D10.1039/D0SC00785D ↗
39. 10.1021/jacs.7b1336410.1021/jacs.7b13364 ↗
40. 10.1021/acsami.9b0165510.1021/acsami.9b01655 ↗
41. 10.1039/C4SC03365E10.1039/C4SC03365E ↗
42. 10.1002/adfm.20170468910.1002/adfm.201704689 ↗
43. 10.1021/ar200195210.1021/ar2001952 ↗
44. 10.1002/anie.20181446210.1002/anie.201814462 ↗
45. 10.1021/jacs.7b0859210.1021/jacs.7b08592 ↗
46. 10.1002/anie.20160250210.1002/anie.201602502 ↗
47. Aggregation‐and crystallization‐induced light emission[C]//organic photonic materials and devices IX
48. 10.1021/jacs.7b1015010.1021/jacs.7b10150 ↗
49. 10.1021/acsnano.8b0313810.1021/acsnano.8b03138 ↗
50. Enzyme‐responsive bioprobes based on the mechanism of aggregation‐induced emission10.1021/acsami.7b14943 ↗
51. 10.1021/acsami.7b1434310.1021/acsami.7b14343 ↗
52. 10.1039/C8TB01519H10.1039/C8TB01519H ↗
53. 10.1002/smll.20180483910.1002/smll.201804839 ↗
54. 10.1002/adma.20160685710.1002/adma.201606857 ↗
55. 10.1002/adhm.20180047710.1002/adhm.201800477 ↗
56. 10.1039/C5SC01733E10.1039/C5SC01733E ↗
57. Frisch MJ · 2009
58. 10.1021/jacs.8b1023510.1021/jacs.8b10235 ↗
59. 10.1016/j.ymeth.2016.06.02510.1016/j.ymeth.2016.06.025 ↗
60. 10.1021/cm503253n10.1021/cm503253n ↗
61. 10.1002/352760162710.1002/3527601627 ↗
62. 10.1039/c3ta15358d10.1039/c3ta15358d ↗
63. 10.1039/C5TA01953B10.1039/C5TA01953B ↗
64. 10.1002/anie.20120463510.1002/anie.201204635 ↗
65. 10.1016/j.apcatb.2018.11.04910.1016/j.apcatb.2018.11.049 ↗
66. Growth inhibition of bacillus subtilis upon interaction between basic dyes and DNA10.1007/BF01699967 ↗
67. 10.1007/BF0161102010.1007/BF01611020 ↗
68. 10.1021/ie302550510.1021/ie3025505 ↗
69. 10.1021/acsami.5b0484210.1021/acsami.5b04842 ↗
70. 10.1021/acsami.5b0969310.1021/acsami.5b09693 ↗
71. 10.1021/acsami.5b0322810.1021/acsami.5b03228 ↗
72. Moulder JF · 1995 · 230
73. 10.1039/C5TA01372K10.1039/C5TA01372K ↗
74. 10.1021/nn501286v10.1021/nn501286v ↗
75. 10.1002/anie.20180499610.1002/anie.201804996 ↗
76. 10.1021/acs.nanolett.9b0027510.1021/acs.nanolett.9b00275 ↗
77. 10.1021/nn102831x10.1021/nn102831x ↗
78. 10.1039/C9TC01665A10.1039/C9TC01665A ↗
79. 10.1021/acs.est.8b0691310.1021/acs.est.8b06913 ↗
80. 10.1039/C9TA00339H10.1039/C9TA00339H ↗