Novel Combination of Efficient Perovskite Solar Cells with Low Temperature Processed Compact TiO2 Layer via Anodic Oxidation
Source abstract
Abstract
In this work, a facile and low temperature processed anodic oxidation approach is proposed for fabricating compact and homogeneous titanium dioxide film (AO-TiO2). In order to realize morphology and thickness control of AO-TiO2, the theory concerning anodic oxidation (AO) is unveiled and the influence of relevant parameters during the process of AO such as electrolyte ingredient and oxidation voltage on AO-TiO2 formation is observed as well. Meanwhile, we demonstrate that the planar perovskite solar cells (p-PSCs) fabricated in ambient air and utilizing optimized AO-TiO2 as electron transport layer (ETL) can deliver repeatable power conversion efficiency (PCE) over 13%, which possess superior open-circuit voltage (Voc) and higher fill factor (FF) compared to its counterpart utilizing conventional high temperature processed compact TiO2 (c-TiO2) as ETL. Through a further comparative study, it is indicated that the improvement of device performance should be attributed to more effective electron collection from perovskite layer to AO-TiO2 and the decrease of device series resistance. Furthermore, hysteresis effect about current density-voltage (J-V) curves in TiO2-based p-PSCs is also unveiled.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Electronic Information and Optical Engineering, Nankai University, Tianjin 300071, China
Funding
National Natural Science Foundation of China
References (29)
Show source-provided references
1. 10.1126/science.124398210.1126/science.1243982 ↗
2. 10.1021/jz500279b10.1021/jz500279b ↗
3. 10.1038/ncomms675710.1038/ncomms6757 ↗
4. 10.1039/c3ee43619e10.1039/c3ee43619e ↗
5. 10.1002/aenm.20140180810.1002/aenm.201401808 ↗
6. 10.1039/c1nr10867k10.1039/c1nr10867k ↗
7. 10.1126/science.aaa927210.1126/science.aaa9272 ↗
8. 10.1126/science.125405010.1126/science.1254050 ↗
9. 10.1021/jacs.5b1107610.1021/jacs.5b11076 ↗
10. 10.1038/nature1234010.1038/nature12340 ↗
11. 10.1038/srep0986310.1038/srep09863 ↗
12. 10.1039/C5RA11081E10.1039/C5RA11081E ↗
13. 10.1021/am503728d10.1021/am503728d ↗
14. 10.1246/cl.15004910.1246/cl.150049 ↗
15. 10.1002/smll.20140353410.1002/smll.201403534 ↗
16. 10.1039/C5TA01526J10.1039/C5TA01526J ↗
17. 10.1002/anie.20100137410.1002/anie.201001374 ↗
18. 10.1038/srep1609810.1038/srep16098 ↗
19. 10.1021/jp052736u10.1021/jp052736u ↗
20. 10.1016/j.jelechem.2008.01.00510.1016/j.jelechem.2008.01.005 ↗
21. 10.1016/j.elecom.2005.04.00810.1016/j.elecom.2005.04.008 ↗
22. 10.1016/S0010-938X(02)00256-110.1016/S0010-938X(02)00256-1 ↗
23. 10.1016/j.electacta.2012.04.07610.1016/j.electacta.2012.04.076 ↗
24. 10.1016/j.solmat.2014.04.02510.1016/j.solmat.2014.04.025 ↗
25. 10.1021/acsami.5b0014910.1021/acsami.5b00149 ↗
26. 10.1002/aenm.20150082910.1002/aenm.201500829 ↗
27. 10.1039/C4EE03664F10.1039/C4EE03664F ↗
28. 10.1021/jz501373f10.1021/jz501373f ↗
29. 10.1002/smll.20140371910.1002/smll.201403719 ↗