Graphite Carbon-Confined Transition Metal Nanoparticle Cocatalysts on TiO 2 Nanosheets for Enhancing Photocatalytic Activity of Hydrogen Evolution
Source abstract
Abstract
The development of noble-metal-free cocatalysts with high activity and durability remains a critical challenge for photocatalytic hydrogen production. Herein, we constructed a family of 0D/2D metal@graphitic-carbon/TiO 2 (M@C/TiO 2 ) nanocomposite photocatalysts, composed of graphitic carbon-confined transition metal nanoparticle (M@C, M = Ni, Co, Cu, and Fe) cocatalysts and TiO 2 nanosheet support. Ni@C/TiO 2 exhibited exceptional photocatalytic hydrogen evolution activity, comparable to that of Pt/TiO 2, which was significantly superior to pristine TiO 2, Ni/TiO 2 and C/TiO 2 by factors of 47, 28, and 6, respectively. The improved photocatalytic activity is attributed to not only the extended light absorption, altered electronic properties, and enhanced charge carrier separation mediated by graphitic carbon-confined transition-metal nanoparticles but also the improved charge carrier transfer through the Ti–O–C–Ni heteroatomic channel between the metal core and the TiO 2 support. Results confirmed the formation of an intimate 0D/2D heterointerface with an optimal band structure, preserved crystallinity, and enriched electron density at Ni active sites. It was also revealed that the graphitic-carbon shell not only protected the metallic nanoparticle from oxidative corrosion but also synergistically enhanced charge separation via interfacial electron transfer mediation. Importantly, the mechanism study indicated that the shallowly trapped electrons that resided at the heterointerface of M@C and TiO 2 contributed to the photocatalytic hydrogen evolution activity, rather than the deeply captured electrons on metal nanoparticles. This work establishes a universal strategy for designing stable, cost-effective transition metal-based cocatalysts through interfacial engineering and protective carbon-shell encapsulation, offering insights into sustainable solar-to-hydrogen conversion systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · TiO2 Photocatalysis and Solar Cells · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science & Engineering, University of Jinan, Nanxinzhuang West Road 336, Jinan, Shandong 250022, P.R. China
Funding
Taishan Scholar Project of Shandong Province · National Natural Science Foundation of China · Science and Technology Program of the University of Jinan
References (52)
Show source-provided references
1. 10.1038/nature1147510.1038/nature11475 ↗
2. 10.1021/acsmaterialslett.4c0138710.1021/acsmaterialslett.4c01387 ↗
3. 10.1038/238037a010.1038/238037a0 ↗
4. 10.1021/cr500189210.1021/cr5001892 ↗
5. 10.1021/cr050053510.1021/cr0500535 ↗
6. 10.1016/j.apcatb.2018.11.08010.1016/j.apcatb.2018.11.080 ↗
7. 10.1016/S1872-2067(19)63294-810.1016/S1872-2067(19)63294-8 ↗
8. 10.1016/j.surfin.2022.10261910.1016/j.surfin.2022.102619 ↗
9. 10.1016/j.rser.2021.11070910.1016/j.rser.2021.110709 ↗
10. 10.1021/acscatal.3c0340510.1021/acscatal.3c03405 ↗
11. 10.1080/01614940.2025.245371410.1080/01614940.2025.2453714 ↗
12. 10.1016/j.carbon.2017.01.05510.1016/j.carbon.2017.01.055 ↗
13. 10.1007/s42765-023-00354-910.1007/s42765-023-00354-9 ↗
14. 10.1016/j.jcis.2023.11.07010.1016/j.jcis.2023.11.070 ↗
15. 10.1016/j.apcatb.2016.07.03310.1016/j.apcatb.2016.07.033 ↗
16. 10.1038/ncomms1066710.1038/ncomms10667 ↗
17. 10.1002/smll.20180170510.1002/smll.201801705 ↗
18. 10.1021/acscatal.5c0005310.1021/acscatal.5c00053 ↗
19. 10.1016/j.jcis.2024.12.12410.1016/j.jcis.2024.12.124 ↗
20. 10.1016/S1872-2067(20)63650-610.1016/S1872-2067(20)63650-6 ↗
21. 10.1016/j.matchemphys.2022.12659710.1016/j.matchemphys.2022.126597 ↗
22. 10.1016/j.chemosphere.2022.13483710.1016/j.chemosphere.2022.134837 ↗
23. 10.1016/j.carbon.2022.02.06310.1016/j.carbon.2022.02.063 ↗
24. 10.1016/j.pmatsci.2019.10059110.1016/j.pmatsci.2019.100591 ↗
25. 10.1002/adma.20231320910.1002/adma.202313209 ↗
26. 10.1016/j.mseb.2025.11856610.1016/j.mseb.2025.118566 ↗
27. 10.1007/s12598-020-01457-710.1007/s12598-020-01457-7 ↗
28. 10.3390/molecules2911270810.3390/molecules29112708 ↗
29. 10.1016/j.jcis.2021.12.15710.1016/j.jcis.2021.12.157 ↗
30. 10.1016/j.jcis.2023.12.15210.1016/j.jcis.2023.12.152 ↗
31. 10.1007/s10854-025-14701-610.1007/s10854-025-14701-6 ↗
32. 10.1016/j.cej.2022.13983410.1016/j.cej.2022.139834 ↗
33. 10.1016/j.ensm.2015.12.00310.1016/j.ensm.2015.12.003 ↗
34. 10.1016/j.apsusc.2020.14794410.1016/j.apsusc.2020.147944 ↗
35. 10.1016/j.apcatb.2019.11825810.1016/j.apcatb.2019.118258 ↗
36. 10.1016/S1872-2067(19)63499-610.1016/S1872-2067(19)63499-6 ↗
37. 10.1016/j.jhazmat.2020.12232410.1016/j.jhazmat.2020.122324 ↗
38. 10.1016/j.jmst.2021.12.07110.1016/j.jmst.2021.12.071 ↗
39. 10.1016/j.jece.2024.11529310.1016/j.jece.2024.115293 ↗
40. 10.1016/j.mtsust.2024.10082310.1016/j.mtsust.2024.100823 ↗
41. 10.1016/j.cej.2023.14419910.1016/j.cej.2023.144199 ↗
42. 10.1021/acs.jpcc.2c0795910.1021/acs.jpcc.2c07959 ↗
43. 10.1126/science.124691310.1126/science.1246913 ↗
44. 10.2138/am-2000-041610.2138/am-2000-0416 ↗
45. 10.1016/j.jmst.2023.07.04410.1016/j.jmst.2023.07.044 ↗
46. 10.3390/catal1302029310.3390/catal13020293 ↗
47. 10.1021/jacs.3c1455810.1021/jacs.3c14558 ↗
48. 10.1021/acsaem.1c0309810.1021/acsaem.1c03098 ↗
49. 10.1007/s10563-022-09362-y10.1007/s10563-022-09362-y ↗
50. 10.1016/j.jpowsour.2023.23306910.1016/j.jpowsour.2023.233069 ↗
51. 10.1016/j.ijhydene.2020.03.18210.1016/j.ijhydene.2020.03.182 ↗
52. 10.1073/pnas.140536511110.1073/pnas.1405365111 ↗