journal article·2018-01-12

Efficient and Stable Pt/TiO2/CdS/Cu2BaSn(S,Se)4 Photocathode for Water Electrolysis Applications

Yihao Zhou, Donghyeop Shin, Edgard Ngaboyamahina, Qiwei Han, Charles B. Parker, David B. Mitzi, Jeffrey T. Glass

ACS Energy Letters· Volume 3· Issue 1
Publisher page

Abstract

The Cu2BaSnS4–xSex (CBTSSe) system has attracted remarkable attention as an emerging chalcogenide semiconductor with desirable electronic and optical properties for solar energy conversion applications. The current study combines sputtered band gap-tailored CBTSSe films with TiO2/CdS protective overlayers to significantly improve photoelectrochemical (PEC) properties as well as device stability in aqueous solutions under AM 1.5G simulated sunlight. The Pt/TiO2/CdS/CBTSSe(x ≈ 3) photocathode exhibits relatively high photocurrent (∼12.08 mA/cm2 at 0 V/RHE, i.e., the highest value reported for CBTSSe-based PEC devices) and stable hydrogen evolution for more than 10 h. The applied TiO2/CdS layers protect the underlying CBTSSe and create desirable band alignment for efficient charge extraction at the heterointerfaces. The present results highlight the opportunities that CBTSSe materials provide as efficient and stable photocathodes for water electrolysis.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties · Copper-based nanomaterials and applications

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

Affiliations

Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708, United States

Department of Chemistry, Duke University, Durham, North Carolina 27708, United States

Photovoltaic Laboratory, Korea Institute of Energy Research, Daejeon 34129, Korea

Department of Electrical & Computer Engineering, Duke University, Durham, North Carolina 27708, United States

Funding

National Science Foundation

References (39)

Show source-provided references
1. 10.1080/15567249.2016.124887410.1080/15567249.2016.1248874 ↗
2. 10.1016/j.ijhydene.2004.10.01110.1016/j.ijhydene.2004.10.011 ↗
3. Van de Krol R. · 201210.1007/978-1-4614-1380-6 ↗
4. 10.1038/238037a010.1038/238037a0 ↗
5. 10.1039/B800489G10.1039/B800489G ↗
6. 10.1016/j.ijhydene.2009.01.05310.1016/j.ijhydene.2009.01.053 ↗
7. 10.1126/science.280.5362.42510.1126/science.280.5362.425 ↗
8. 10.1002/anie.20140648310.1002/anie.201406483 ↗
9. 10.1038/srep0216310.1038/srep02163 ↗
10. 10.1038/nmat301710.1038/nmat3017 ↗
11. 10.1038/nnano.2014.27710.1038/nnano.2014.277 ↗
12. 10.1021/ja312653y10.1021/ja312653y ↗
13. 10.1039/C5TA01058F10.1039/C5TA01058F ↗
14. 10.1021/jacs.5b0901510.1021/jacs.5b09015 ↗
15. 10.1021/acsenergylett.6b0045310.1021/acsenergylett.6b00453 ↗
16. 10.1016/j.jphotochem.2004.04.00610.1016/j.jphotochem.2004.04.006 ↗
17. 10.1021/jacs.6b0959510.1021/jacs.6b09595 ↗
18. 10.1021/am402096r10.1021/am402096r ↗
19. 10.1021/acs.chemmater.6b0183210.1021/acs.chemmater.6b01832 ↗
20. 10.1063/1.482025010.1063/1.4820250 ↗
21. 10.1002/adma.20160694510.1002/adma.201606945 ↗
22. 10.1039/C6TA06702F10.1039/C6TA06702F ↗
23. 10.1021/acs.jpclett.6b0201010.1021/acs.jpclett.6b02010 ↗
24. 10.1021/acs.chemmater.6b0334710.1021/acs.chemmater.6b03347 ↗
25. 10.1039/C5TA01259G10.1039/C5TA01259G ↗
26. 10.1016/j.apsusc.2004.08.01310.1016/j.apsusc.2004.08.013 ↗
27. 10.3390/catal703009310.3390/catal7030093 ↗
28. 10.1002/zaac.1976426030810.1002/zaac.19764260308 ↗
29. Hersh P. A. · 2008
30. 10.1002/aenm.20160236610.1002/aenm.201602366 ↗
31. 10.1021/acs.jpcc.5b0206810.1021/acs.jpcc.5b02068 ↗
32. 10.1116/1.367202710.1116/1.3672027 ↗
33. 10.1002/aenm.20160180310.1002/aenm.201601803 ↗
34. 10.1021/acs.chemmater.7b0263810.1021/acs.chemmater.7b02638 ↗
35. 10.1103/PhysRevB.83.12520110.1103/PhysRevB.83.125201 ↗
36. 10.1002/adma.20100229010.1002/adma.201002290 ↗
37. 10.1002/adfm.20110296610.1002/adfm.201102966 ↗
38. 10.1039/C4CP04057K10.1039/C4CP04057K ↗
39. 10.1002/aenm.20150194910.1002/aenm.201501949 ↗