journal article·2022-01

Reversible Photochromic Properties of Ti2O3(H2O)2(C2O4) ⋅ H2O Material

Kangkai Hu, Lei E, Dan Zhao, Zhengang Guo, Bo Zhang

ChemNanoMat· Volume 8· Issue 1
Publisher page

Abstract

Abstract Potassium titanyl oxalate is used as the titanium source and HCl as growth promoter. Ti2O3(H2O)2(C2O4) ⋅ H2O, with hexagonal prism and spherical polyhedral morphology, has been synthesized by one‐step hydrothermal method at 120 °C for 6∼12 h, and the particle size range is 8–12 μm. Ti2O3(H2O)2(C2O4) ⋅ H2O prepared in this research has excellent reversible photochromic properties. It is a kind of P‐type photochromic compound, which is achromatic or colorless. The equilibrium time of discoloration or fading is 30 min. The photochromic mechanism research shows that the photochromic properties of Ti2O3(H2O)2(C2O4) ⋅ H2O are caused by the continuous reaction of Ti4+, Ti3+ with ecb−, VO++ in unsaturated cationic compounds.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Photochromic and Fluorescence Chemistry · TiO2 Photocatalysis and Solar Cells · Polyoxometalates: Synthesis and Applications

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

Affiliations

School of Materials Science and Engineering Tianjin Chengjian University Jinjing Road on the 26th, Xiqing District Tianjin 300384 P. R. China

School of Materials Sun Yat-sen University No.66, Gongchang Road, Guangming District Shenzhen Guangdong 518107 P. R. China

Tianjin Key Laboratory of Building Green Functional Materials Tianjin Chengjian University Jinjing Road on the 26th, Xiqing District Tianjin 300384 P. R. China

Funding

Natural Science Foundation of Tianjin City

References (31)

Show source-provided references
1.
2. Bouas-Laurent H. · Photochromism · 2001 · 73 · 639
3. 10.1002/adma.20120152110.1002/adma.201201521 ↗
4. 10.1039/C7CS00630F10.1039/C7CS00630F ↗
5. 10.1016/j.polymer.2020.12231110.1016/j.polymer.2020.122311 ↗
6. 10.1002/ejoc.20190181410.1002/ejoc.201901814 ↗
7. 10.1021/acsami.9b2318910.1021/acsami.9b23189 ↗
8. 10.1007/s00339-020-03574-710.1007/s00339-020-03574-7 ↗
9.
10. 10.1021/acs.nanolett.0c0041410.1021/acs.nanolett.0c00414 ↗
11. 10.1016/j.apsusc.2015.12.19510.1016/j.apsusc.2015.12.195 ↗
12. 10.1039/D0CE00167H10.1039/D0CE00167H ↗
13. 10.1021/acsami.0c0518210.1021/acsami.0c05182 ↗
14. 10.1021/jacs.0c1018310.1021/jacs.0c10183 ↗
15.
16. 10.1021/acs.jpcc.9b1056310.1021/acs.jpcc.9b10563 ↗
17. 10.1038/ncomms1111810.1038/ncomms11118 ↗
18. 10.1039/D1CC00920F10.1039/D1CC00920F ↗
19. 10.1002/slct.20200022410.1002/slct.202000224 ↗
20.
21. 10.1039/C8CE00330K10.1039/C8CE00330K ↗
22. 10.1039/C9CE01694E10.1039/C9CE01694E ↗
23. J. F. Moulder W. F. Stickle P. E. Sobol K. D. Bomben Handbook of X-ray photoelectron spectroscopy Physical Electronics Inc. 1995 p. 72.
24.
25. Kim J. W. · Mater. Res. Soc. Symp. Proc. · 2003 · 764 · 327
26. 10.1134/1.131757110.1134/1.1317571 ↗
27.
28. S. Simons W. William The Sadtler handbook of infrared spectra Sadtler Research Laboratories 1978 p. 66;
29. K. Nakamoto Infrared and Raman spectra of inoganic and coordination compounds (Part B: aplications in coordination organometallic and bioinorganic chemistry) John Wiley & Sons Inc. 2009 p. 132–154.10.1002/9780470405888 ↗
30. P. J. Larkin Infrared and Raman spectroscopy Elsevier Inc. 2011 p. 55–62.10.1016/B978-0-12-386984-5.10004-7 ↗
31. 10.1016/j.apcatb.2017.01.02510.1016/j.apcatb.2017.01.025 ↗