Noble Metal-Free Photocatalysts Consisting of Graphitic Carbon Nitride, Nickel Complex, and Nickel Oxide Nanoparticles for Efficient Hydrogen Generation
Source abstract
Abstract
A facile and simple synthetic route is developed to prepare earth-abundant and noble metal-free hybrid photocatalysts, which are composed of graphitic carbon nitride (CN), nickel complex, and NiOx nanoparticles. Bimolecular nucleophilic substitution reaction was employed to attach a nickel complex onto a graphitic CN framework through covalent bonds to support its high loading and dispersion. NiOx nanoparticles were further incorporated into the catalysts to serve as a hole-transporting medium to improve the separation of photogenerated carriers for higher photocatalytic activity. Both yNiL/CN and yNiL/NiOx/CN exhibit superb H2 evolution activity. The optimum H2 evolution rate of the binary photocatalysts yNiL/CN reaches 303.3 μmol·h–1·g–1, whereas that of the ternary photocatalysts yNiL/NiOx/CN reaches 524.1 μmol·h–1·g–1, and the apparent quantum efficiency reaches 1.46% at 450 nm. This finding reveals that coordination of a nickel complex is significant in promoting photocatalytic performance, and the incorporation of NiOx nanoparticles as a hole-transporting medium is beneficial for separation of the photogenerated charge carriers. The novel hybrid system offers a new horizon for designing transition-metal complex-modified graphitic CN as noble metal-free and highly active photocatalysts for efficient visible light-driven hydrogen generation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Perovskite Materials and Applications · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640, People’s Republic of China
Funding
National Natural Science Foundation of China
References (56)
Show source-provided references
1. 10.1038/nmat231710.1038/nmat2317 ↗
2. 10.1021/ja211637p10.1021/ja211637p ↗
3. 10.1038/natrevmats.2017.3010.1038/natrevmats.2017.30 ↗
4. 10.1021/acs.chemrev.6b0007510.1021/acs.chemrev.6b00075 ↗
5. 10.1103/physrevb.87.08520210.1103/physrevb.87.085202 ↗
6. 10.1021/jz500546b10.1021/jz500546b ↗
7. 10.1016/j.apcatb.2013.05.04410.1016/j.apcatb.2013.05.044 ↗
8. 10.1016/j.apsusc.2014.10.16110.1016/j.apsusc.2014.10.161 ↗
9. 10.1002/cctc.20160092810.1002/cctc.201600928 ↗
10. 10.1002/asia.20180108310.1002/asia.201801083 ↗
11. 10.1021/ja306258410.1021/ja3062584 ↗
12. 10.1002/slct.20160203110.1002/slct.201602031 ↗
13. 10.1016/j.matlet.2017.04.04310.1016/j.matlet.2017.04.043 ↗
14. 10.1016/j.apcatb.2017.07.03410.1016/j.apcatb.2017.07.034 ↗
15. 10.1002/adma.20150269610.1002/adma.201502696 ↗
16. 10.1021/jacs.8b0855210.1021/jacs.8b08552 ↗
17. 10.1021/jacs.7b0026610.1021/jacs.7b00266 ↗
18. 10.1021/acssuschemeng.7b0078710.1021/acssuschemeng.7b00787 ↗
19. 10.1021/am509213x10.1021/am509213x ↗
20. 10.1021/acs.chemrev.6b0039810.1021/acs.chemrev.6b00398 ↗
21. 10.1021/acs.nanolett.7b0531410.1021/acs.nanolett.7b05314 ↗
22. 10.1002/adfm.20170640310.1002/adfm.201706403 ↗
23. 10.1016/j.nanoen.2017.02.02110.1016/j.nanoen.2017.02.021 ↗
24. 10.1002/adma.20140539110.1002/adma.201405391 ↗
25. 10.1002/adma.20120445310.1002/adma.201204453 ↗
26. 10.1002/adfm.20120092210.1002/adfm.201200922 ↗
27. 10.1002/adfm.20130360010.1002/adfm.201303600 ↗
28. 10.1002/smll.20170359910.1002/smll.201703599 ↗
29. 10.1002/adma.20180012810.1002/adma.201800128 ↗
30. 10.1016/j.carbon.2018.07.03610.1016/j.carbon.2018.07.036 ↗
31. 10.1002/adma.20150205710.1002/adma.201502057 ↗
32. 10.1002/adma.20140057310.1002/adma.201400573 ↗
33. 10.1002/adma.20160619810.1002/adma.201606198 ↗
34. 10.1002/adfm.20120226910.1002/adfm.201202269 ↗
35. 10.1038/am.2014.7810.1038/am.2014.78 ↗
36. 10.1039/c8na00029h10.1039/c8na00029h ↗
37. 10.1016/j.carbon.2018.03.08910.1016/j.carbon.2018.03.089 ↗
38. 10.1016/j.apsusc.2016.03.02510.1016/j.apsusc.2016.03.025 ↗
39. 10.1039/c8ta03048k10.1039/c8ta03048k ↗
40. 10.1016/0022-1902(74)80621-410.1016/0022-1902(74)80621-4 ↗
41. Liu J. N. · Turk. J. Chem. · 2007 · 31 · 623
42. 10.1021/jacs.6b0199710.1021/jacs.6b01997 ↗
43. 10.1039/c6ra00933f10.1039/c6ra00933f ↗
44. 10.1021/jp503477x10.1021/jp503477x ↗
45. 10.1002/aenm.20180113910.1002/aenm.201801139 ↗
46. 10.1016/j.apcatb.2018.02.00610.1016/j.apcatb.2018.02.006 ↗
47. 10.1039/c8ta05723k10.1039/c8ta05723k ↗
48. 10.1039/c7cc02400b10.1039/c7cc02400b ↗
49. 10.1016/j.nanoen.2016.12.04410.1016/j.nanoen.2016.12.044 ↗
50. 10.1016/j.apcatb.2015.01.02410.1016/j.apcatb.2015.01.024 ↗
51. 10.1016/j.materresbull.2017.01.03410.1016/j.materresbull.2017.01.034 ↗
52. 10.1021/jacs.7b0036910.1021/jacs.7b00369 ↗
53. 10.1016/j.inoche.2016.08.02210.1016/j.inoche.2016.08.022 ↗
54. 10.1002/cssc.20120049010.1002/cssc.201200490 ↗
55. 10.1016/j.bmc.2017.06.04110.1016/j.bmc.2017.06.041 ↗
56. 10.1126/science.aaa314510.1126/science.aaa3145 ↗