Photocatalytic Hydrogen Production with Conjugated Polymers as Photosensitizers
Source abstract
Abstract
Artificial photosynthesis is a chemical process that aims to capture energy from sunlight to produce solar fuels. Light absorption by a robust and efficient photosensitizer is one of the key steps in solar energy conversion. However, common photosensitizers, including [Ru(bpy)3]2+ (RuP), remain far from the ideal. In this work, we exploited the performance of conjugated polymers (CPs) as photosensitizers in photodriven hydrogen evolution in aqueous solution (pH 6). Interestingly, CPs, such as poly(fluorene-co-phenylene) derivative (429 mmolH2·gCP–1·h–1), exhibit steady and high reactivity toward hydrogen evolution; this performance can rival that of a phosphonated RuP under the same conditions, indicating that CPs are promising metal-free photosensitizers for future applications in photocatalysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · CO2 Reduction Techniques and Catalysts · Catalytic Processes in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Funding
Ministry of Science and Technology of the People's Republic of China · Tsinghua University · National Natural Science Foundation of China · Central People's Government of the People's Republic of China
References (56)
Show source-provided references
1. 10.1073/pnas.060339510310.1073/pnas.0603395103 ↗
2. 10.1039/c3cs60405e10.1039/c3cs60405e ↗
3. 10.1021/ar500160510.1021/ar5001605 ↗
4. 10.1039/c3cs35531d10.1039/c3cs35531d ↗
5. 10.1021/ar400076j10.1021/ar400076j ↗
6. 10.1039/c6cs00436a10.1039/c6cs00436a ↗
7. 10.1021/ar500140r10.1021/ar500140r ↗
8. 10.1021/jacs.6b1014610.1021/jacs.6b10146 ↗
9. 10.1021/jacs.5b1275810.1021/jacs.5b12758 ↗
10. 10.1021/jacs.6b1297610.1021/jacs.6b12976 ↗
11. 10.1038/nenergy.2017.2110.1038/nenergy.2017.21 ↗
12. 10.1021/cr100164510.1021/cr1001645 ↗
13. 10.1002/cssc.20140288510.1002/cssc.201402885 ↗
14. 10.1039/c5cs00733j10.1039/c5cs00733j ↗
15. 10.1002/anie.20120418010.1002/anie.201204180 ↗
16. 10.1039/c4ra10767e10.1039/c4ra10767e ↗
17. 10.1039/c0cc04658b10.1039/c0cc04658b ↗
18. 10.1021/cr300503r10.1021/cr300503r ↗
19. 10.1021/ja410592d10.1021/ja410592d ↗
20. 10.1039/c6ee00629a10.1039/c6ee00629a ↗
21. 10.1021/ja413001p10.1021/ja413001p ↗
22. 10.1021/jacs.5b0165010.1021/jacs.5b01650 ↗
23. 10.1038/3211810.1038/32118 ↗
24. 10.1021/acs.chemrev.6b0041910.1021/acs.chemrev.6b00419 ↗
25. 10.1063/1.10503910.1063/1.105039 ↗
26. 10.1038/1639310.1038/16393 ↗
27. 10.1126/science.280.5370.174110.1126/science.280.5370.1741 ↗
28. 10.1021/ja00155a02310.1021/ja00155a023 ↗
29. 10.1021/cr050149z10.1021/cr050149z ↗
30. 10.1038/nphoton.2012.1110.1038/nphoton.2012.11 ↗
31. 10.1002/anie.20160701810.1002/anie.201607018 ↗
32. 10.1039/c7ee00751e10.1039/c7ee00751e ↗
33. 10.1021/ar400136b10.1021/ar400136b ↗
34. 10.1126/science.120586410.1126/science.1205864 ↗
35. 10.1021/ja109755f10.1021/ja109755f ↗
36. 10.1002/1521-4095(20020304)14:5<361::aid-adma361>3.0.co;2-910.1002/1521-4095(20020304)14:5<361::aid-adma361>3.0.co;2-9 ↗
37. 10.1021/ja036507210.1021/ja0365072 ↗
38. 10.1002/adma.20140063610.1002/adma.201400636 ↗
39. 10.1002/1521-3773(20020503)41:9<1548::aid-anie1548>3.0.co;2-i10.1002/1521-3773(20020503)41:9<1548::aid-anie1548>3.0.co;2-i ↗
40. 10.1002/adfm.20110084010.1002/adfm.201100840 ↗
41. 10.1021/ja904492x10.1021/ja904492x ↗
42. 10.1021/cr200263w10.1021/cr200263w ↗
43. 10.1002/anie.20170237610.1002/anie.201702376 ↗
44. 10.1039/cs981100004910.1039/cs9811000049 ↗
45. 10.1021/j100211a01410.1021/j100211a014 ↗
46. 10.1016/s0022-0728(68)80086-510.1016/s0022-0728(68)80086-5 ↗
47. Turro N. J. · 2010
48. 10.1002/anie.20160435510.1002/anie.201604355 ↗
49. 10.1021/acs.chemmater.6b0147710.1021/acs.chemmater.6b01477 ↗
50. 10.1021/acsami.7b0006910.1021/acsami.7b00069 ↗
51. 10.1021/jp411710b10.1021/jp411710b ↗
52. 10.1021/jacs.5b1085310.1021/jacs.5b10853 ↗
53. 10.1016/j.electacta.2016.12.08110.1016/j.electacta.2016.12.081 ↗
54. 10.1039/c5sc01349f10.1039/c5sc01349f ↗
55. 10.1021/acs.inorgchem.5b0044510.1021/acs.inorgchem.5b00445 ↗
56. 10.1021/om200709z10.1021/om200709z ↗