3D Porous Pyramid Heterostructure Array Realizing Efficient Photo‐Electrochemical Performance
Source abstract
Abstract
Abstract Direct photo‐electrochemical (PEC) water splitting is of great practical interest for developing a sustainable energy systems, but remains a big challenge owing to sluggish charge separation, low efficiency, and poor stability. Herein, a 3D porous In2O3/In2S3 pyramid heterostructure array on a fluorine‐doped tin oxide substrate is fabricated by an ion exchange–induced synthesis strategy. Based on the synergistic structural and electronic modulations from density functional theory calculations and experimental observations, 3D porous In2O3/In2S3 photoanode by the protective layer delivers a low onset potential of ≈0.02 V versus reversible hydrogen electrode (RHE), the highest photocurrent density of 8.2 mA cm−2 at 1.23 V versus RHE among all the In2S3 photoanodes reported to date, an incident photon‐to‐current efficiency of 76% at 400 nm, and high stability over 20 h for PEC water splitting are reported. This work provides an alternative promising prototype for the design and construction of novel heterostructures in robust PEC water splitting applications.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Fine Chemicals DUT‐KTH Joint Education and Research Center on Molecular Devices Dalian University of Technology (DUT) Dalian 116024 China
Department of Chemistry KTH Royal Institute of Technology 10044 Stockholm Sweden
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities · Energimyndigheten · Knut och Alice Wallenbergs Stiftelse
References (69)
Show source-provided references
1. 10.1126/science.aat696710.1126/science.aat6967 ↗
2. 10.1038/nature1906010.1038/nature19060 ↗
3. 10.1002/aenm.20170055510.1002/aenm.201700555 ↗
4. 10.1038/nature1645510.1038/nature16455 ↗
5. 10.1021/jacs.9b0623910.1021/jacs.9b06239 ↗
6. 10.1126/science.aad331710.1126/science.aad3317 ↗
7. 10.1016/j.mtchem.2018.11.00210.1016/j.mtchem.2018.11.002 ↗
8. 10.1016/j.jechem.2017.04.01910.1016/j.jechem.2017.04.019 ↗
9. 10.1016/j.jechem.2017.09.03610.1016/j.jechem.2017.09.036 ↗
10. 10.1016/j.jechem.2017.12.01410.1016/j.jechem.2017.12.014 ↗
11. 10.1038/s41467-018-03543-y10.1038/s41467-018-03543-y ↗
12. 10.1038/s41467-019-09788-510.1038/s41467-019-09788-5 ↗
13. 10.1002/aenm.20180079510.1002/aenm.201800795 ↗
14. 10.1002/aenm.20160226010.1002/aenm.201602260 ↗
15. 10.1038/nenergy.2017.8710.1038/nenergy.2017.87 ↗
16. 10.1039/C7EE01747B10.1039/C7EE01747B ↗
17. 10.1016/j.nanoen.2015.04.02210.1016/j.nanoen.2015.04.022 ↗
18. 10.1002/anie.20160297310.1002/anie.201602973 ↗
19. 10.1039/C8EE02768D10.1039/C8EE02768D ↗
20. 10.1021/acsenergylett.6b0031710.1021/acsenergylett.6b00317 ↗
21. 10.1016/j.jechem.2018.01.00410.1016/j.jechem.2018.01.004 ↗
22. 10.1016/j.jechem.2017.05.01110.1016/j.jechem.2017.05.011 ↗
23. 10.1016/j.jechem.2017.09.00610.1016/j.jechem.2017.09.006 ↗
24. 10.1002/adma.20160152510.1002/adma.201601525 ↗
25. 10.1002/aenm.20180016510.1002/aenm.201800165 ↗
26. 10.1002/aenm.20170106010.1002/aenm.201701060 ↗
27. 10.1021/nl402690210.1021/nl4026902 ↗
28. 10.1002/aenm.20190094010.1002/aenm.201900940 ↗
29. 10.1002/aenm.20160043710.1002/aenm.201600437 ↗
30. 10.1002/aenm.20190099410.1002/aenm.201900994 ↗
31. 10.1002/adma.20180048610.1002/adma.201800486 ↗
32. 10.1002/aenm.20180140310.1002/aenm.201801403 ↗
33. 10.1039/C5EE03802B10.1039/C5EE03802B ↗
34. 10.1002/aenm.20160086410.1002/aenm.201600864 ↗
35. 10.1016/j.nanoen.2017.04.03710.1016/j.nanoen.2017.04.037 ↗
36. 10.1002/aenm.20180009410.1002/aenm.201800094 ↗
37. 10.1002/aenm.20130061110.1002/aenm.201300611 ↗
38. 10.1002/anie.20120467510.1002/anie.201204675 ↗
39. 10.1002/anie.20150341010.1002/anie.201503410 ↗
40. 10.1002/aenm.20170111410.1002/aenm.201701114 ↗
41. 10.1002/anie.20181163210.1002/anie.201811632 ↗
42. 10.1039/C6NR06969J10.1039/C6NR06969J ↗
43. 10.1007/s40820-018-0199-z10.1007/s40820-018-0199-z ↗
44. 10.1039/C7NR06182J10.1039/C7NR06182J ↗
45. 10.1016/j.apsusc.2012.05.14110.1016/j.apsusc.2012.05.141 ↗
46. 10.1016/j.ijhydene.2017.04.28310.1016/j.ijhydene.2017.04.283 ↗
47. 10.1039/C5CC09601D10.1039/C5CC09601D ↗
48. 10.1016/j.jpowsour.2013.09.05410.1016/j.jpowsour.2013.09.054 ↗
49. 10.1002/adma.20170566610.1002/adma.201705666 ↗
50. 10.1039/C3EE44031A10.1039/C3EE44031A ↗
51. 10.1002/smll.20140097010.1002/smll.201400970 ↗
52. 10.1002/anie.20130268010.1002/anie.201302680 ↗
53. 10.1002/adfm.20160046110.1002/adfm.201600461 ↗
54. 10.1002/admi.20150042810.1002/admi.201500428 ↗
55. 10.1002/adfm.20170678510.1002/adfm.201706785 ↗
56. 10.1021/acs.nanolett.6b0209410.1021/acs.nanolett.6b02094 ↗
57. 10.1016/j.chempr.2017.10.01810.1016/j.chempr.2017.10.018 ↗
58. 10.1039/c3cp51722e10.1039/c3cp51722e ↗
59. 10.1039/C5CP05833C10.1039/C5CP05833C ↗
60. 10.1021/acssuschemeng.6b0009010.1021/acssuschemeng.6b00090 ↗
61. 10.1039/C5TA01958C10.1039/C5TA01958C ↗
62. 10.1126/science.125142810.1126/science.1251428 ↗
63. 10.1038/nmat304710.1038/nmat3047 ↗
64. 10.1021/acs.nanolett.5b0492910.1021/acs.nanolett.5b04929 ↗
65. 10.1039/c3ta13912c10.1039/c3ta13912c ↗
66. 10.1039/c2sc20874a10.1039/c2sc20874a ↗
67. 10.1021/nn305709210.1021/nn3057092 ↗
68. 10.1021/acsami.7b1913910.1021/acsami.7b19139 ↗
69. 10.1002/adfm.20180139710.1002/adfm.201801397 ↗