Titanium Nitride Protected Cuprous Oxide Photocathode for Stable and Efficient Water Reduction
Source abstract
Abstract
Photoelectrochemical water splitting for hydrogen production provides a pollution-free and sustainable way to alleviate the over-reliance on fossil fuels. Cu2O is one of the photocathodes most concerned with superior performance, but it suffers from photocorrosion in the electrolyte, which is unfavorable to hydrogen production. Therefore, a reasonable and simple protection strategy to inhibit the photocorrosion of Cu2O is urgently needed in the long term hydrogen production device. In this work, we proposed a Cu2O-based photocathode protection strategy, which uses atomic layer deposition technology to deposit TiN thin film as the protective layer. The optimized photocathode shows remarkably improved stability: the photocurrent density maintains the initial value of −1.4 mA cm–2 for more than 35 min at 0 V vs RHE; after 1-h testing, it still remains at 71% of the initial value, with 16-fold enhancement in comparison with that of the bare photocathode. This work offers a way to solve the stability issue of unstable photoelectrodes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Copper-based nanomaterials and applications · ZnO doping and properties · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Electronic Science and Engineering and Tianjin Key Laboratory of Process Control and Green Technology for Pharmaceutical Industry, Nankai University, Tianjin 300350, China
School of Mechanics and Photoelectric Physics, Anhui University of Science and Technology, Huainan 232001, China
Tianjin Pharmaceuticals Research Organization Co., Ltd., and Green Technology for Pharmaceutical Industry, Nankai University, Tianjin 300462, China
Funding
National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1038/s41929-018-0077-610.1038/s41929-018-0077-6 ↗
2. 10.1016/j.ijhydene.2019.06.18410.1016/j.ijhydene.2019.06.184 ↗
3. 10.1039/C4EE03271C10.1039/C4EE03271C ↗
4. 10.1002/aenm.20170232310.1002/aenm.201702323 ↗
5. 10.1039/C6CS00918B10.1039/C6CS00918B ↗
6. 10.1039/D0EE02397C10.1039/D0EE02397C ↗
7. 10.1021/acs.nanolett.5b0492910.1021/acs.nanolett.5b04929 ↗
8. 10.1039/C5EE00250H10.1039/C5EE00250H ↗
9. 10.1039/C7CY00040E10.1039/C7CY00040E ↗
10. 10.1002/pssb.20124812810.1002/pssb.201248128 ↗
11. 10.1039/C4RA13896A10.1039/C4RA13896A ↗
12. 10.1039/c2ee22063f10.1039/c2ee22063f ↗
13. 10.1021/am404527q10.1021/am404527q ↗
14. 10.1149/1.139322110.1149/1.1393221 ↗
15. 10.1021/cm991054e10.1021/cm991054e ↗
16. 10.1149/1.283085010.1149/1.2830850 ↗
17. 10.1038/nmat301710.1038/nmat3017 ↗
18. 10.1021/ja309523t10.1021/ja309523t ↗
19. 10.1021/nn305709210.1021/nn3057092 ↗
20. 10.1021/acsaem.9b0129010.1021/acsaem.9b01290 ↗
21. 10.1016/j.electacta.2010.08.03510.1016/j.electacta.2010.08.035 ↗
22. 10.1039/C4TA02402H10.1039/C4TA02402H ↗
23. 10.1039/C8TA12186A10.1039/C8TA12186A ↗
24. 10.1039/C6TA05200B10.1039/C6TA05200B ↗
25. 10.1039/c3cc44076a10.1039/c3cc44076a ↗
26. 10.1002/ange.20120358510.1002/ange.201203585 ↗
27. 10.1016/S0169-4332(03)00005-910.1016/S0169-4332(03)00005-9 ↗
28. 10.1016/j.tsf.2018.07.00810.1016/j.tsf.2018.07.008 ↗
29. 10.1088/2053-1591/ab166210.1088/2053-1591/ab1662 ↗
30. 10.1039/c3ce40985f10.1039/c3ce40985f ↗
31. 10.1016/j.jhazmat.2012.06.04410.1016/j.jhazmat.2012.06.044 ↗