journal article·2024-02-13

Formation Mechanism for Particulate Y2Ti2O5S2 Photocatalyst by the Solid-State Reaction

Lihua Lin, Mamiko Nakabayashi, Daling Lu, Takashi Hisatomi, Tsuyoshi Takata, Kazunari Domen

Chemistry of Materials· Volume 36· Issue 3
Publisher page

Abstract

Y 2 Ti 2 O 5 S 2 (YTOS) is a stable oxysulfide photocatalyst applicable to water splitting under visible light with wavelengths of up to 650 nm. However, the activity of YTOS in the overall water-splitting reaction is still low, possibly because YTOS particles prepared by a solid-state reaction (SSR) method have large sizes and high defect density. Therefore, understanding the formation mechanism is indispensable for synthesizing YTOS with the desired physical properties to improve its performance. In this study, we investigated the formation mechanism for YTOS produced by an SSR method. The results indicated that Y 2 Ti 2 O 7, Y 2 O 2 S, and TiS 2 are key intermediate phases in the formation of YTOS. Detailed formation steps are proposed for YTOS particles as they pass through these intermediate phases. By controlling the formation process for these intermediates, it was possible to prepare YTOS with a reduced particle size and enhanced activity for photocatalytic H 2 evolution.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Gas Sensing Nanomaterials and Sensors · Perovskite Materials and Applications

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

Affiliations

Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University, Nagano 380-8553, Japan

Institute of Engineering Innovation, School of Engineering, The University of Tokyo, 2-11-16, Yayoi, Bunkyo-ku, Tokyo 113-8656, Japan

Office of University Professors, The University of Tokyo, Tokyo 113-86556, Japan

Funding

New Energy and Industrial Technology Development Organization

References (33)

Show source-provided references
1. 10.1126/science.aad192010.1126/science.aad1920 ↗
2. 10.1039/c2cs35230c10.1039/c2cs35230c ↗
3. 10.1039/C8CS00542G10.1039/C8CS00542G ↗
4. 10.1021/acs.chemrev.9b0020110.1021/acs.chemrev.9b00201 ↗
5. 10.1039/D1CS01182K10.1039/D1CS01182K ↗
6. 10.1038/s41586-020-2278-910.1038/s41586-020-2278-9 ↗
7. 10.1038/s41586-021-03907-310.1038/s41586-021-03907-3 ↗
8. 10.1038/s41586-022-05183-110.1038/s41586-022-05183-1 ↗
9. 10.1038/nmat231710.1038/nmat2317 ↗
10. 10.1038/s41467-022-28146-610.1038/s41467-022-28146-6 ↗
11. 10.1039/c3ee40831k10.1039/c3ee40831k ↗
12. 10.1039/C3CS60378D10.1039/C3CS60378D ↗
13. 10.1016/j.trechm.2020.06.00610.1016/j.trechm.2020.06.006 ↗
14. 10.1038/s41563-019-0399-z10.1038/s41563-019-0399-z ↗
15. 10.1006/jssc.1995.106210.1006/jssc.1995.1062 ↗
16. 10.1016/j.jssc.2004.04.02310.1016/j.jssc.2004.04.023 ↗
17. 10.1039/b107659k10.1039/b107659k ↗
18. 10.1021/ic030173010.1021/ic0301730 ↗
19. 10.1006/jssc.2002.949210.1006/jssc.2002.9492 ↗
20. 10.1021/ja026964310.1021/ja0269643 ↗
21. 10.1021/cm034540h10.1021/cm034540h ↗
22. 10.1021/jp036890x10.1021/jp036890x ↗
23. 10.1039/c3cp54668c10.1039/c3cp54668c ↗
24. 10.1021/acs.jpclett.6b0180210.1021/acs.jpclett.6b01802 ↗
25. 10.1021/acs.jpcc.7b1208710.1021/acs.jpcc.7b12087 ↗
26. 10.1007/s11164-020-04329-y10.1007/s11164-020-04329-y ↗
27. 10.1002/cptc.20220020910.1002/cptc.202200209 ↗
28. 10.1002/anie.20231060710.1002/anie.202310607 ↗
29. 10.1039/D2TA06895H10.1039/D2TA06895H ↗
30. 10.1080/0371750X.2011.1060017210.1080/0371750X.2011.10600172 ↗
31. 10.1002/pssb.20145129710.1002/pssb.201451297 ↗
32. 10.1039/c1cc10665a10.1039/c1cc10665a ↗
33. 10.1039/a809737b10.1039/a809737b ↗