journal article·2025-01Open access

Dual Electric Field Coupling with Tunable Schottky Barrier Synergistically Regulating Electronic Configuration in CoP@Ni‐CdS Heterojunction for Efficient Photocatalytic H2 Evolution

Xinlei Zhang, Fei Wu, Guicun Li, Lei Wang, Jianfeng Huang, Aili Song, Alan Meng, Zhenjiang Li

Advanced Functional Materials· Volume 35· Issue 2

Abstract

Abstract Designing and exploiting visible‐light‐responsive materials that converts solar into chemical energy is promising in achieving green energy sustainability, but addressing low electron–hole separation efficiency and sluggish surface kinetic process remains formidable challenges. Herein, a novel CoP@Ni‐CdS Schottky junction composed of Ni‐doped CdS nanorods and quasi‐metallic CoP nanoparticles is constructed via a simple hydrothermal–calcination method. Experiments and theoretical calculations demonstrate that magnetic Ni‐doping not only induces a spin‐polarized electric field and enhances the built‐in interfacial electric field strength, but also rises the Schottky barrier height at the heterointerface, which synergistically accelerates the separation efficiency of photoinduced charges and modulates the electronic configuration of the active site to optimize the adsorption–desorption behaviors for H2O molecules and H* intermediates. Therefore, the designed CoP@Ni‐CdS catalyst exhibits an exceptional photocatalytic performance with H2 evolution rate of 42.14 mmol g−1 h−1 with the apparent quantum efficiencies of 16.8% at 420 nm, which is 14.14 and 2.21 times higher than that of pristine CdS and Ni‐CdS, respectively. This work provides in‐depth insights into fabricating dual electric fields, tuning the Schottky barrier and modulating the electronic configuration of active sites in Schottky heterojunction for ameliorative photocatalytic activity.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Quantum Dots Synthesis And Properties · Copper-based nanomaterials and applications

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

Affiliations

College of Materials Science and Engineering Qingdao University of Science and Technology Qingdao 266042 P. R. China

Key Laboratory of Optic‐electric Sensing and Analytical Chemistry for Life Science College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 P. R. China

School of Material Science and Engineering Shaanxi University of Science and Technology Xi'an 710021 P. R. China

Qingdao Huanghai University Qingdao 266000 P. R. China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Shandong Province · China Postdoctoral Science Foundation

References (62)

Show source-provided references
1. 10.1039/D1CS01182K10.1039/D1CS01182K ↗
2. 10.1038/s41586-022-05399-110.1038/s41586-022-05399-1 ↗
3. 10.1016/j.joule.2023.12.00510.1016/j.joule.2023.12.005 ↗
4. 10.1038/s41570-022-00366-w10.1038/s41570-022-00366-w ↗
5. 10.1021/acs.chemrev.9b0020110.1021/acs.chemrev.9b00201 ↗
6. 10.1002/adma.20210519510.1002/adma.202105195 ↗
7. 10.1021/jacs.3c1382710.1021/jacs.3c13827 ↗
8. 10.1038/s41929-023-01069-110.1038/s41929-023-01069-1 ↗
9. 10.1038/s41467-024-47022-z10.1038/s41467-024-47022-z ↗
10. 10.1002/adfm.20220135710.1002/adfm.202201357 ↗
11. 10.1002/anie.20230780810.1002/anie.202307808 ↗
12. 10.1002/adma.20220017210.1002/adma.202200172 ↗
13. 10.1002/adfm.20230407210.1002/adfm.202304072 ↗
14. 10.1002/adfm.20220325210.1002/adfm.202203252 ↗
15. 10.1021/jacs.3c0399010.1021/jacs.3c03990 ↗
16. 10.1002/smll.20240076910.1002/smll.202400769 ↗
17. 10.1002/smll.20230331810.1002/smll.202303318 ↗
18. 10.1021/acscatal.4c0001610.1021/acscatal.4c00016 ↗
19. 10.1002/advs.20220177310.1002/advs.202201773 ↗
20. 10.1002/anie.20230455910.1002/anie.202304559 ↗
21. 10.1002/adfm.20230232510.1002/adfm.202302325 ↗
22. 10.1021/acscatal.2c0540110.1021/acscatal.2c05401 ↗
23. 10.1002/advs.20230929310.1002/advs.202309293 ↗
24. 10.1002/anie.20230305410.1002/anie.202303054 ↗
25. 10.1002/anie.20230123910.1002/anie.202301239 ↗
26. 10.1016/j.apcatb.2022.12147010.1016/j.apcatb.2022.121470 ↗
27. 10.1016/j.apsusc.2021.15181710.1016/j.apsusc.2021.151817 ↗
28. 10.1021/acsnano.1c0652410.1021/acsnano.1c06524 ↗
29. 10.1016/j.cej.2022.14042010.1016/j.cej.2022.140420 ↗
30. 10.1002/smll.20220775810.1002/smll.202207758 ↗
31. 10.1002/adfm.20231660410.1002/adfm.202316604 ↗
32. 10.1016/j.apcatb.2023.12337310.1016/j.apcatb.2023.123373 ↗
33. 10.1002/anie.20230630510.1002/anie.202306305 ↗
34. 10.1016/j.apcatb.2022.12132110.1016/j.apcatb.2022.121321 ↗
35. 10.1016/j.apcatb.2024.12380910.1016/j.apcatb.2024.123809 ↗
36. 10.1002/anie.20211605710.1002/anie.202116057 ↗
37. 10.1016/j.apcatb.2022.12191010.1016/j.apcatb.2022.121910 ↗
38. 10.1016/j.apcatb.2022.12186310.1016/j.apcatb.2022.121863 ↗
39. 10.1016/j.seppur.2023.12341210.1016/j.seppur.2023.123412 ↗
40. 10.1002/anie.20231317210.1002/anie.202313172 ↗
41. 10.1002/adfm.20221313110.1002/adfm.202213131 ↗
42. 10.1016/j.nanoen.2023.10838110.1016/j.nanoen.2023.108381 ↗
43. 10.1002/aenm.20220382710.1002/aenm.202203827 ↗
44. 10.1002/adfm.20211199910.1002/adfm.202111999 ↗
45. 10.1016/j.apcatb.2023.12286010.1016/j.apcatb.2023.122860 ↗
46. 10.1016/j.apcatb.2022.12200410.1016/j.apcatb.2022.122004 ↗
47. 10.1016/j.apcatb.2023.12339810.1016/j.apcatb.2023.123398 ↗
48. 10.1016/j.cej.2021.13106910.1016/j.cej.2021.131069 ↗
49. 10.1016/j.apcatb.2023.12354310.1016/j.apcatb.2023.123543 ↗
50. 10.1002/adfm.20240006510.1002/adfm.202400065 ↗
51. 10.1002/smll.20230040210.1002/smll.202300402 ↗
52. 10.1021/jacs.4c0426410.1021/jacs.4c04264 ↗
53. 10.1021/jacs.2c0606010.1021/jacs.2c06060 ↗
54. 10.1016/j.apcatb.2022.12133710.1016/j.apcatb.2022.121337 ↗
55. 10.1016/j.apsusc.2023.15762510.1016/j.apsusc.2023.157625 ↗
56. 10.1016/j.apcatb.2024.12397810.1016/j.apcatb.2024.123978 ↗
57. 10.1002/smll.20240061110.1002/smll.202400611 ↗
58. 10.1002/anie.20231892710.1002/anie.202318927 ↗
59. 10.1016/j.scib.2024.03.00310.1016/j.scib.2024.03.003 ↗
60. 10.1002/adma.20230090210.1002/adma.202300902 ↗
61. 10.1016/j.apcatb.2024.12389310.1016/j.apcatb.2024.123893 ↗
62. 10.1002/adfm.20230184010.1002/adfm.202301840 ↗