A Case Study on a Soluble Dibenzothiophene-S,S-dioxide-Based Conjugated Polyelectrolyte for Photocatalytic Hydrogen Production: The Film versus the Bulk Material
Source abstract
Abstract
Most of the traditional polymeric photocatalysts are generally insoluble in organic solvents, which might exclude their compatibility with large-area processing technology. Herein, we have synthesized a novel quaternized ammonium conjugated polyelectrolyte (PSO-FNBr) that can be processed to prepare an active film by a drop-casting method. PSO-FNBr shows a remarkably enhanced hydrogen evolution rate (HER) of 20.5 mmol h–1 g–1 in the thin film form in comparison to that of the powder form. Furthermore, we prepared a new type of thin film-based photocatalytic device, which provided a rare example of a “three-in-one” (rapid sampling + easy-to-use + cost-effective) photocatalytic system. The PSO-FNBr thin film over the Pt substrate can maintain a competitive HER, even though the Pt substrate was recycled and reused 50 times. Considering the features of impressive activity and low cost, we believe that PSO-FNBr will be a promising material for potential application in photocatalysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Covalent Organic Framework Applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430205, P. R. China
School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710062, P. R. China
Funding
Hubei Provincial Department of Education · MOE Key Laboratory of Optoelectronic Chemical Materials and Devices, Jianghan University
References (52)
Show source-provided references
1. 10.1039/B800489G10.1039/B800489G ↗
2. 10.1021/cr100164510.1021/cr1001645 ↗
3. 10.1002/anie.20160737510.1002/anie.201607375 ↗
4. 10.1039/C9EE01935A10.1039/C9EE01935A ↗
5. 10.1002/adma.20150003310.1002/adma.201500033 ↗
6. 10.1039/C5EE01895A10.1039/C5EE01895A ↗
7. 10.1039/C5CS00767D10.1039/C5CS00767D ↗
8. 10.1038/ncomms950810.1038/ncomms9508 ↗
9. 10.1016/j.apcatb.2020.11917410.1016/j.apcatb.2020.119174 ↗
10. 10.1021/acscatal.9b0219510.1021/acscatal.9b02195 ↗
11. 10.1039/D0TA10165F10.1039/D0TA10165F ↗
12. 10.1039/C4CS00103F10.1039/C4CS00103F ↗
13. Wang W. · Adv. Sci. · 2017 · 4 · 160037110.1002/advs.201600371 ↗
14. 10.1002/aenm.20170047910.1002/aenm.201700479 ↗
15. 10.1038/natrevmats.2017.5010.1038/natrevmats.2017.50 ↗
16. 10.1002/ente.20150014210.1002/ente.201500142 ↗
17. 10.1039/D0EE01213K10.1039/D0EE01213K ↗
18. 10.1016/j.joule.2017.12.00910.1016/j.joule.2017.12.009 ↗
19. Yanagida S. · J. Chem. Soc., Perkin Trans. · 1996 · 2 · 196310.1039/P29960001963 ↗
20. 10.1002/asia.20200024710.1002/asia.202000247 ↗
21. Dai C. · Sol. RRL. · 2018 · 3 · 180025510.1002/solr.201800255 ↗
22. 10.1002/adfm.20180815610.1002/adfm.201808156 ↗
23. 10.1016/j.nanoen.2019.04.02710.1016/j.nanoen.2019.04.027 ↗
24. 10.1021/acsmaterialslett.9b0032510.1021/acsmaterialslett.9b00325 ↗
25. 10.1021/acsapm.9b0085910.1021/acsapm.9b00859 ↗
26. 10.1016/j.apcatb.2020.11885210.1016/j.apcatb.2020.118852 ↗
27. 10.1038/s41467-018-07420-610.1038/s41467-018-07420-6 ↗
28. 10.1002/smll.20180183910.1002/smll.201801839 ↗
29. 10.1038/s41557-018-0141-510.1038/s41557-018-0141-5 ↗
30. 10.1039/C8TA11383A10.1039/C8TA11383A ↗
31. 10.1016/j.apcatb.2019.01.01010.1016/j.apcatb.2019.01.010 ↗
32. 10.1039/D0TA06159J10.1039/D0TA06159J ↗
33. 10.1039/D0TA12425G10.1039/D0TA12425G ↗
34. 10.1021/jacs.9b0359110.1021/jacs.9b03591 ↗
35. 10.1021/acsenergylett.8b0185310.1021/acsenergylett.8b01853 ↗
36. 10.1039/C3CS60425J10.1039/C3CS60425J ↗
37. 10.1021/ar300227e10.1021/ar300227e ↗
38. 10.1021/acsenergylett.6b0039110.1021/acsenergylett.6b00391 ↗
39. 10.1016/j.polymer.2017.06.04710.1016/j.polymer.2017.06.047 ↗
40. 10.1021/acs.macromol.5b0113710.1021/acs.macromol.5b01137 ↗
41. 10.1002/adfm.20180451210.1002/adfm.201804512 ↗
42. 10.1021/acssuschemeng.8b0563710.1021/acssuschemeng.8b05637 ↗
43. 10.1016/j.isci.2019.02.00710.1016/j.isci.2019.02.007 ↗
44. 10.1021/acs.macromol.9b0055110.1021/acs.macromol.9b00551 ↗
45. 10.1039/C9TA06425G10.1039/C9TA06425G ↗
46. 10.1039/C9TA06219J10.1039/C9TA06219J ↗
47. 10.1039/D0TA01200A10.1039/D0TA01200A ↗
48. 10.1039/D0NR05801G10.1039/D0NR05801G ↗
49. 10.1016/j.apcatb.2019.11806710.1016/j.apcatb.2019.118067 ↗
50. 10.1021/acsami.7b0142810.1021/acsami.7b01428 ↗
51. 10.1002/adma.20080242010.1002/adma.200802420 ↗
52. 10.1002/adma.20170603410.1002/adma.201706034 ↗