Photocatalytic H 2 O 2 Synthesis at NiS/NiSe-Coated Nanoporous Poly(dimethylsiloxane) Membrane Triphase Interfaces
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Photocatalytic hydrogen peroxide (H 2 O 2 ) production offers a sustainable alternative, though it faces challenges such as low oxygen (O 2 ) diffusion in the electrolyte and high electron–hole recombination rates. This study introduces an air–liquid–solid triphase reaction interface using a nickel sulfide/nickel selenide (NiS/NiSe) photocatalyst on a nanoporous hydrophobic poly(dimethylsiloxane) (PDMS) membrane, enhancing O 2 accessibility and catalytic efficiency. The triphase system generates 1041.2 μmol g –1 h –1 H 2 O 2 without an external O 2 supply, significantly outperforming the conventional diphase system, which produces 286 μmol g –1 h –1 with a constant external O 2 supply. This enhancement is due to the synergy between (i) the nanoporous hydrophobic PDMS membrane, which enables continuous O 2 diffusion to the catalyst surface, and (ii) the NiS/NiSe S-scheme heterojunction, which promotes charge separation. The mechanistic aspects and reaction pathway for H 2 O 2 production are elaborated in the study using electrochemical techniques.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gas Sensing Nanomaterials and Sensors · TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, Indian Institute of Technology Hyderabad, Kandi, Sangareddy 502285, Telangana, India
The School of Chemical Engineering
Oklahoma State University
Funding
Indian Institute of Technology Hyderabad · Oklahoma State University
References (37)
Show source-provided references
1. 10.1126/science.aay184410.1126/science.aay1844 ↗
2. Myers R. L. · 200710.5040/9798400605284 ↗
3. 10.1002/anie.20050377910.1002/anie.200503779 ↗
4. 10.1016/j.checat.2023.10087010.1016/j.checat.2023.100870 ↗
5. 10.1039/D4CC01577K10.1039/D4CC01577K ↗
6. 10.1038/s41570-019-0110-610.1038/s41570-019-0110-6 ↗
7. 10.1002/anie.20191160910.1002/anie.201911609 ↗
8. 10.1002/anie.20140793810.1002/anie.201407938 ↗
9. 10.1021/acsestengg.1c0045610.1021/acsestengg.1c00456 ↗
10. 10.1016/j.cej.2022.13848910.1016/j.cej.2022.138489 ↗
11. 10.1038/s41467-020-15597-y10.1038/s41467-020-15597-y ↗
12. 10.1038/nmat231710.1038/nmat2317 ↗
13. 10.1021/acscatal.5b0040810.1021/acscatal.5b00408 ↗
14. 10.1016/j.apcatb.2020.11860210.1016/j.apcatb.2020.118602 ↗
15. 10.1021/jacs.6b0580610.1021/jacs.6b05806 ↗
16. 10.1002/anie.20200484110.1002/anie.202004841 ↗
17. 10.1002/adma.20029002010.1002/adma.200290020 ↗
18. 10.1021/jacs.5b1272810.1021/jacs.5b12728 ↗
19. 10.1021/ja410529q10.1021/ja410529q ↗
20. 10.1021/jacs.3c1246510.1021/jacs.3c12465 ↗
21. 10.1016/j.apcatb.2022.12106610.1016/j.apcatb.2022.121066 ↗
22. 10.1016/j.isci.2019.06.02310.1016/j.isci.2019.06.023 ↗
23. 10.1016/j.jallcom.2020.15681010.1016/j.jallcom.2020.156810 ↗
24. 10.1016/j.ijhydene.2024.04.10110.1016/j.ijhydene.2024.04.101 ↗
25. 10.1002/adma.20190043010.1002/adma.201900430 ↗
26. 10.1002/smll.20190508310.1002/smll.201905083 ↗
27. 10.1016/j.apsusc.2020.14697610.1016/j.apsusc.2020.146976 ↗
28. 10.1016/j.apcatb.2022.12143410.1016/j.apcatb.2022.121434 ↗
29. 10.1038/s41598-020-59714-910.1038/s41598-020-59714-9 ↗
30. 10.1016/j.ijhydene.2020.04.04510.1016/j.ijhydene.2020.04.045 ↗
31. 10.1016/j.commatsci.2013.11.04810.1016/j.commatsci.2013.11.048 ↗
32. 10.1021/acs.langmuir.0c0053810.1021/acs.langmuir.0c00538 ↗
33. 10.1049/mnl.2017.023010.1049/mnl.2017.0230 ↗
34. 10.1016/j.ijhydene.2021.02.16010.1016/j.ijhydene.2021.02.160 ↗
35. 10.1016/j.apcatb.2025.12569310.1016/j.apcatb.2025.125693 ↗
36. 10.1016/j.jcis.2025.13894110.1016/j.jcis.2025.138941 ↗
37. 10.1016/S1872-2067(24)60275-510.1016/S1872-2067(24)60275-5 ↗