journal article·2021-08-25

Interior/Interface Modification of Textured Perovskite for Enhanced Photovoltaic Outputs of Planar Solar Cells by an In Situ Growth Passivation Technology

Mingyue Wang, Lin Fan, Wanhong Lü, Qinghua Sun, Xiaohan Wang, Fengyou Wang, Jinghai Yang, Huilian Liu, Lili Yang

ACS Applied Materials & Interfaces· Volume 13· Issue 33
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Abstract

To compensate for the photoelectric losses of planar heterojunction perovskite solar cells (PSCs), the development of high-quality textured absorbers with excellent light-harvesting ability and carrier extraction/transfer efficiency is of great significance to achieve a high-efficiency stable photovoltaic output. In this paper, we propose an in situ growth passivation technique to construct high-performance textured absorbers by adding a 2-amino-4-chlorophenol (AC) modifier consisting of multiple groups during the growth of textured perovskite. Initially, according to the Ostwald ripening mechanism, the strongly polar dimethylformamide (DMF) was used as the etchant to systematically study its synergistic effect on the morphology evolution, crystallization kinetics, light-trapping capability, and photovoltaic loss of textured absorbers. An appropriate amount of DMF induces formamidinium cations (FA+) to replace methylammonium cations (MA+) in the perovskite lattice while etching the absorber to form a texture configuration, which effectively broadens the spectral absorption range, thus greatly improving the light-trapping capacity and short-circuit current density of planar PSCs. In contrast, excess DMF deteriorates the device performance due to the excessive corrosion of the perovskite. Moreover, the introduction of the AC modifier is of great significance for passivating deep-level defects and accelerating the charge extraction/transfer. Owing to the electron-donating nature of the Lewis base, the hydroxyl groups with a higher electron density in AC molecules can better coordinate with Pb2+ ion defects, which effectively improves the crystallinity of the textured perovskite, thus suppressing the nonradiative recombination and ultimately improving the photovoltaic outputs of modified devices, particularly the fill factor and the open-circuit voltage. Thus, the photovoltaic performance of the AC-modified planar PSC is significantly better than that of the conventional textured device, with a reverse efficiency of 21.18% and forward efficiency of 20.77%. Owing to the synergistic effect of (1) the superior optical properties of the textured perovskite induced by DMF and (2) excellent charge dynamics driven by AC, the functionalized devices without encapsulation also exhibited good photovoltaic output stability and reproducibility. This work provides novel insights into the growth mechanism of textured absorbers and paves the way for more efficient and stable planar PSCs.
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Research context

OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Organic Electronics and Photovoltaics

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

Affiliations

Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University, Changchun 130103, China

National Demonstration Center for Experimental Physics Education, Jilin Normal University, Siping 136000, China

Funding

Ministry of Science and Technology of the People's Republic of China · Department of Science and Technology of Jilin Province · National Natural Science Foundation of China · Thirteenth Five-YearProgram for Science and Technology of Education Department of Jilin Province · Innovation and EntrepreneurshipTraining Program, Jilin Normal University

References (55)

Show source-provided references
1. 10.1002/adma.20200220210.1002/adma.202002202 ↗
2. 10.1039/D0EE02017F10.1039/D0EE02017F ↗
3. 10.1039/D0EE02859B10.1039/D0EE02859B ↗
4. Best Research-Cell Efficiency Chart; https://www.nrel.gov/pv/cell-efficiency.html.
5. 10.1016/j.nanoen.2020.10449510.1016/j.nanoen.2020.104495 ↗
6. 10.1002/adfm.20080068310.1002/adfm.200800683 ↗
7. 10.1016/j.nanoen.2016.08.00110.1016/j.nanoen.2016.08.001 ↗
8. 10.1016/j.jpowsour.2020.22886210.1016/j.jpowsour.2020.228862 ↗
9. 10.1002/adma.20180428410.1002/adma.201804284 ↗
10. 10.1038/s41467-019-10985-510.1038/s41467-019-10985-5 ↗
11. Wang P. · Adv. Sci. · 2020 · 7 · 200042110.1002/advs.202000421 ↗
12. 10.1002/adfm.20190973810.1002/adfm.201909738 ↗
13. 10.1002/aenm.20160092010.1002/aenm.201600920 ↗
14. 10.1039/D0EE03387A10.1039/D0EE03387A ↗
15. 10.1039/C6TA11004E10.1039/C6TA11004E ↗
16. 10.1016/j.cej.2020.12409110.1016/j.cej.2020.124091 ↗
17. 10.1002/aenm.20190225610.1002/aenm.201902256 ↗
18. Wang S. · Adv. Funct. Mater. · 2020 · 7 · 1903009
19. 10.1063/1.492215010.1063/1.4922150 ↗
20. 10.1016/j.nanoen.2019.01.01410.1016/j.nanoen.2019.01.014 ↗
21. 10.1002/aenm.20190405410.1002/aenm.201904054 ↗
22. 10.1016/j.nanoen.2020.10523710.1016/j.nanoen.2020.105237 ↗
23. 10.1016/j.nanoen.2020.10450510.1016/j.nanoen.2020.104505 ↗
24. 10.1021/acsami.0c2197510.1021/acsami.0c21975 ↗
25. 10.1002/adfm.20200805210.1002/adfm.202008052 ↗
26. 10.1021/acsenergylett.0c0113010.1021/acsenergylett.0c01130 ↗
27. 10.1038/s41467-021-22049-810.1038/s41467-021-22049-8 ↗
28. Tumen-Ulzii G. · Adv. Mater. · 2020 · 30 · 190503510.1002/adma.201905035 ↗
29. Wang F. · Adv. Sci. · 2019 · 6 · 180117010.1002/advs.201801170 ↗
30. 10.1021/acsami.7b0850410.1021/acsami.7b08504 ↗
31. 10.1039/C9TC02149C10.1039/C9TC02149C ↗
32. 10.1002/adfm.20190083010.1002/adfm.201900830 ↗
33. 10.1002/adts.20180003010.1002/adts.201800030 ↗
34. 10.1016/j.optcom.2016.05.07410.1016/j.optcom.2016.05.074 ↗
35. Ye T. · Adv. Funct. Mater. · 2017 · 27 · 160454510.1002/adfm.201604545 ↗
36. 10.1002/smll.20160197410.1002/smll.201601974 ↗
37. 10.1016/j.nanoen.2019.02.02310.1016/j.nanoen.2019.02.023 ↗
38. 10.1016/j.cej.2020.12630310.1016/j.cej.2020.126303 ↗
39. 10.1039/C7TA00973A10.1039/C7TA00973A ↗
40. 10.1039/C6EE03586H10.1039/C6EE03586H ↗
41. 10.1002/anie.20201714810.1002/anie.202017148 ↗
42. Sun Y. · Chem. Eng. J. · 2020 · 413 · 12738710.1016/j.cej.2020.127387 ↗
43. 10.1016/j.nanoen.2017.08.00910.1016/j.nanoen.2017.08.009 ↗
44. Xiong S. · Sol. RRL · 2020 · 5 · 190052910.1002/solr.201900529 ↗
45. 10.1002/solr.20190019710.1002/solr.201900197 ↗
46. 10.1021/acsami.0c1125010.1021/acsami.0c11250 ↗
47. 10.1016/j.nanoen.2019.10422410.1016/j.nanoen.2019.104224 ↗
48. 10.1021/acsaem.8b0000110.1021/acsaem.8b00001 ↗
49. 10.1016/j.nanoen.2016.06.04110.1016/j.nanoen.2016.06.041 ↗
50. Wang Y. · Nano Energy · 2018 · 58 · 55610.1016/j.nanoen.2018.06.085 ↗
51. 10.1016/j.nanoen.2018.06.05410.1016/j.nanoen.2018.06.054 ↗
52. 10.1021/acsphotonics.8b0009910.1021/acsphotonics.8b00099 ↗
53. 10.1016/j.nanoen.2017.02.00210.1016/j.nanoen.2017.02.002 ↗
54. 10.1002/solr.20180026810.1002/solr.201800268 ↗
55. 10.1021/acsenergylett.0c0164210.1021/acsenergylett.0c01642 ↗