Synthesis and up-conversion properties of Ho 3+ -Yb 3+ -F − tri-doped TiO 2 nanoparticles and their application in dye-sensitized solar cells
Source abstract
Abstract
Abstract A series of Ho 3+ -Yb 3+ -F − tri-doped TiO 2 nanoparticles (abbreviated as UP-F-TiO 2 NPs) were prepared using a hydrosol−hydrothermal method, and their phase structure, morphology and luminescent properties were investigated. These nanoparticles were utilized to prepare a photoanode of dye-sensitized solar cells (DSSCs). Based on the up-conversion spectra of UP-F-TiO 2 NPs, an up-conversion mechanism is proposed. The results indicate that the UP-F-TiO 2 NPs were a mixture of anatase and rutile nanoparticles, and the mass fraction of the anatase phase first increases and then decreases with increasing incorporation of F − ions into UC-F-TiO 2 NPs, while the un-doped TiO 2 nanoparticles are in the rutile phase. The average sizes of the UP-F-TiO 2 NPs are estimated to be 10 nm. The HRTEM shows clear lattice fringes with spacings of 0.347 nm and 0.323 nm that correspond to the d spacings of the (101) facets in anatase TiO 2 and the (110) facets in rutile TiO 2 , respectively. Under the excitation of 980 nm NIR light, the UP-F-TiO 2 NPs exhibit a stronger emission band centered at 543 nm and two relatively weaker bands located at 667 nm and 751 nm. The DSSC assembled with a bilayer-structured UP-F-TiO 2 NP photoanode has a 35.2% enhancement in conversion efficiency compared with DSSCs assembled with un-doped TiO 2 photoanodes.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (25)
Show source-provided references
1. Mathew · Nat. Chem. · 2014 · 6 · 24210.1038/nchem.1861 ↗
2. Aguilar · Appl. Phys. A · 2015 · 121 · 126110.1007/s00339-015-9503-7 ↗
3. Sun · Acc. Chem. Res. · 2014 · 47 · 100110.1021/ar400218t ↗
4. Wang · Acc.Chem. Res. · 2011 · 44 · 32210.1021/ar100129p ↗
5. Li · J. Power Sour. · 2014 · 264 · 25410.1016/j.jpowsour.2014.04.100 ↗
6. Yang · Nanotechnology · 2014 · 25 · 48200110.1088/0957-4484/25/48/482001 ↗
7. Pandey · Mater. Res. Bull. · 2014 · 57 · 15610.1016/j.materresbull.2014.04.071 ↗
8. Gao · Mater. Res. Bull. · 2016 · 80 · 25610.1016/j.materresbull.2016.03.024 ↗
9. Zhou · Chem. Rev. · 2015 · 115 · 39510.1021/cr400478f ↗
10. de Wild · Energy Environ. Sci · 2011 · 4 · 483510.1039/c1ee01659h ↗
11. Du · Opt. Mater. Expr. · 2016 · 6 · 189610.1364/OME.6.001896 ↗
12. Yao · Electrochim. Acta · 2015 · 154 · 27310.1016/j.electacta.2014.12.095 ↗
13. Gai · Chem. Rev. · 2014 · 114 · 234310.1021/cr4001594 ↗
14. Yu · Inorg. Chem. · 2014 · 53 · 804510.1021/ic501041h ↗
15. Wei · J. Renewable Sustainable Energy · 2013 · 5 · 03310110.1063/1.4803525 ↗
16. Sang · Chem. Rev. · 2014 · 114 · 928310.1021/cr400629p ↗
17. Patel · J. Alloys Compd. · 2011 · 509 · 42710.1016/j.jallcom.2011.01.086 ↗
18. Lage · J. Phys. Condens. Matter. · 2004 · 16 · 320710.1088/0953-8984/16/18/021 ↗
19. Zhang · Materials Chem. Phys. · 2005 · 16610.1016/j.matchemphys.2004.11.007 ↗
20. Yildirim · Ceram. Int. · 2016 · 1057910.1016/j.ceramint.2016.03.131 ↗
21. Moulder · J. Chemical Phys. Lett. · 1963 · 99 · 7
22. Yurddaskal · J. Alloy. Compd. · 2015 · 651 · 5910.1016/j.jallcom.2015.08.064 ↗
23. Han · RSC. Adv. · 2015 · 5 · 2473710.1039/C5RA00378D ↗
24. Gao · J. Nanosci. Nanotechnol. · 2016 · 16 · 375410.1166/jnn.2016.11812 ↗
25. Zhou · Nanoscale · 2014 · 6 · 205210.1039/C3NR04315K ↗