journal article·2016

CdS/ZnS Co-Sensitized Hierarchical TiO2Nanotree Array with Rutile/Anatase Junctions for Enhanced Photoelectrochemical Performance

Zhuang Wang, Xingzhi Wang, Xishun Jiang, Jiajia Tao, Zezhou Gong, Yunlang Cheng, Miao Zhang, Lei Yang, Jianguo Lv, Gang He, Zhaoqi Sun

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Abstract

Hetero-structured TiO 2 nanotree arrays on flurine-doped tin oxide (FTO) substrates were deposited by a two-step hydrothermal method, CdS/ZnS core-shell quantum dots (CdS/ZnS QDs) were deposited by a successive ionic layer absorption and reaction (SILAR) process. The TiO 2 nanotree array is composed of a trunk-branch structure where the trunk is rutile TiO 2 nanorod array and the branch is anatase TiO 2 nanosheets standing on the trunk. Morphology, optical properties and photoelectrochemical (PEC) performances were investigated in detail. After the deposition of CdS/ZnS QDs, TiO 2 nanotree array photoanode shows much better PEC performance compared to TiO 2 nanorod array photoanode that sensitized nanotree array show a higher photocurrent desity (1.5 mA/cm 2 ) at 1.0 V and almost 2-fold current density (0.29 mA/cm 2 ) than sensitized nanorod array (1.0 mA/cm 2 and 0.15 mA/cm 2 ) in the measurement of linear sweep voltammetry (LSV) and transient photocurrent, respectively. This result is due to the enlarged surface specific area for more quantum dots loading, and also due to the rutile/anatase junctions formed on the boundary of trunks and branches, leading to an effective charge separating and transporting. It suggests that the hetero-structured TiO 2 nanotree array is very promising to be applied in highly efficient photoanodes for energy devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · TiO2 Photocatalysis and Solar Cells · Quantum Dots Synthesis And Properties

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

References (39)

Show source-provided references
1. 10.1007/s10854-015-3997-910.1007/s10854-015-3997-9 ↗
2. 10.1039/c0nr00427h10.1039/c0nr00427h ↗
3. 10.1021/nl204296810.1021/nl2042968 ↗
4. 10.1021/am200377g10.1021/am200377g ↗
5. 10.1021/jp412674g10.1021/jp412674g ↗
6. 10.1039/C5NR00069F10.1039/C5NR00069F ↗
7. 10.1016/j.ijhydene.2008.07.06810.1016/j.ijhydene.2008.07.068 ↗
8. 10.1016/j.apcatb.2012.06.00710.1016/j.apcatb.2012.06.007 ↗
9. 10.1021/cr200047710.1021/cr2000477 ↗
10. 10.1166/jnn.2003.15810.1166/jnn.2003.158 ↗
11. 10.1063/1.363818110.1063/1.3638181 ↗
12. 10.1016/j.jelechem.2014.12.03010.1016/j.jelechem.2014.12.030 ↗
13. 10.1021/nl202818810.1021/nl2028188 ↗
14. 10.1039/c3nr04462a10.1039/c3nr04462a ↗
15. 10.1088/0957-4484/15/12/03010.1088/0957-4484/15/12/030 ↗
16. 10.1038/nmat138710.1038/nmat1387 ↗
17. 10.1088/0957-4484/19/50/50560410.1088/0957-4484/19/50/505604 ↗
18. 10.1063/1.344291310.1063/1.3442913 ↗
19. 10.1039/c2jm15442k10.1039/c2jm15442k ↗
20. 10.1021/am401746b10.1021/am401746b ↗
21. 10.1038/nature0696410.1038/nature06964 ↗
22. 10.1016/j.jallcom.2012.01.12610.1016/j.jallcom.2012.01.126 ↗
23. 10.1002/adfm.20080117310.1002/adfm.200801173 ↗
24. 10.1021/nn103371v10.1021/nn103371v ↗
25. 10.1021/nn800141e10.1021/nn800141e ↗
26. 10.1021/jp908694310.1021/jp9086943 ↗
27. 10.1021/jp303681410.1021/jp3036814 ↗
28. 10.1039/c1cp20290a10.1039/c1cp20290a ↗
29. 10.1021/jp311846r10.1021/jp311846r ↗
30. 10.1063/1.344735610.1063/1.3447356 ↗
31. 10.1039/c3cp44719g10.1039/c3cp44719g ↗
32. 10.1021/ja807897210.1021/ja8078972 ↗
33. 10.1021/nl202939210.1021/nl2029392 ↗
34. 10.1016/j.solmat.2015.05.02910.1016/j.solmat.2015.05.029 ↗
35. 10.1149/2.0641603jes10.1149/2.0641603jes ↗
36. 10.1016/j.elecom.2012.05.03710.1016/j.elecom.2012.05.037 ↗
37. 10.1038/srep2540510.1038/srep25405 ↗
38. 10.1016/j.jcis.2011.08.07310.1016/j.jcis.2011.08.073 ↗
39. 10.1021/ja208418z10.1021/ja208418z ↗