Methylammonium Bromide Assisted Crystallization for Enhanced Lead‐Free Double Perovskite Photovoltaic Performance
Source abstract
Abstract
Abstract Cs2AgBiBr6, has recently gained wide attention as a possible alternative to lead‐halide perovskites, considering the nontoxicity and improved stability. However, this double perovskite suffers from defects, especially deep electron traps, severely hampering the photovoltaic performance. This work reports a simple method to control the double perovskite crystallization by adding volatile salts into the precursor solution. X‐ray diffraction patterns reveal that the organic cation with suitable radius (such as methylammonium, MA+) is introduced into the perovskite lattice, forming an organic/inorganic mixed double perovskite intermediate phase. The organic salt is thereafter fully evaporated during high temperature annealing, and the all‐inorganic double perovskite is obtained with dense surface and less pin‐holes. From optical and electrical characterization, it is concluded that the Cs2AgBiBr6 film exhibits high quality, with higher light absorptance and emission. Reduced trap density and longer carrier lifetime are also observed. The improved Cs2AgBiBr6 film is beneficial for efficient carrier collection with suppressed defect‐assisted recombination. With this strategy, a power conversion efficiency (PCE) of 2.53% is achieved for the champion Cs2AgBiBr6‐based solar cell device, which is significantly higher compared to the control device with 1.43% PCE. This work is therefore helpful for further improvement of inorganic lead‐free perovskite materials for optoelectronic applications.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Solid-state spectroscopy and crystallography
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry‐Ångström Physical Chemistry Uppsala University Uppsala 75120 Sweden
School of Materials Science and Engineering Beihang University Beijing 100191 China
Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK
Department of Applied Physical Chemistry KTH Royal Institute of Technology Stockholm 114 28 Sweden
Funding
National Natural Science Foundation of China
References (56)
Show source-provided references
1. 10.1021/ja809598r10.1021/ja809598r ↗
2. 10.1038/s41586-021-03406-510.1038/s41586-021-03406-5 ↗
3. 10.1038/nnano.2014.14910.1038/nnano.2014.149 ↗
4. 10.1002/adma.20140227110.1002/adma.201402271 ↗
5. 10.1038/nphoton.2014.13410.1038/nphoton.2014.134 ↗
6. 10.1002/aenm.20150096310.1002/aenm.201500963 ↗
7. 10.1038/nmat457210.1038/nmat4572 ↗
8. 10.1021/acsenergylett.6b0049910.1021/acsenergylett.6b00499 ↗
9. 10.1021/acs.jpclett.7b0158410.1021/acs.jpclett.7b01584 ↗
10. 10.1021/jacs.6b0964510.1021/jacs.6b09645 ↗
11. 10.1016/j.joule.2018.06.01710.1016/j.joule.2018.06.017 ↗
12. 10.1002/aenm.20180315010.1002/aenm.201803150 ↗
13. 10.1021/acs.jpclett.6b0104110.1021/acs.jpclett.6b01041 ↗
14. 10.1021/acs.chemmater.5b0423110.1021/acs.chemmater.5b04231 ↗
15. 10.1021/jacs.5b1329410.1021/jacs.5b13294 ↗
16. 10.1021/acs.jpcc.7b0013810.1021/acs.jpcc.7b00138 ↗
17. 10.1002/admi.20180046410.1002/admi.201800464 ↗
18. 10.1021/acs.jpclett.6b0037610.1021/acs.jpclett.6b00376 ↗
19. 10.1021/acsenergylett.0c0102010.1021/acsenergylett.0c01020 ↗
20. 10.1002/adma.20170624610.1002/adma.201706246 ↗
21. 10.1038/s41566-017-0012-410.1038/s41566-017-0012-4 ↗
22. 10.1002/advs.20170075910.1002/advs.201700759 ↗
23. 10.1002/cphc.20180034610.1002/cphc.201800346 ↗
24. 10.1007/s40843-020-1346-010.1007/s40843-020-1346-0 ↗
25. 10.1039/C7TA06816F10.1039/C7TA06816F ↗
26. 10.1021/acs.nanolett.9b0023810.1021/acs.nanolett.9b00238 ↗
27. 10.1016/j.orgel.2019.06.03710.1016/j.orgel.2019.06.037 ↗
28. 10.1039/C9TA10422D10.1039/C9TA10422D ↗
29. 10.1021/acsenergylett.8b0087110.1021/acsenergylett.8b00871 ↗
30. 10.1021/acs.chemmater.9b0424310.1021/acs.chemmater.9b04243 ↗
31. 10.1002/adfm.20200155710.1002/adfm.202001557 ↗
32. 10.1021/jacs.0c1273910.1021/jacs.0c12739 ↗
33. 10.1021/jacs.0c1278610.1021/jacs.0c12786 ↗
34. 10.1038/s41467-017-02088-w10.1038/s41467-017-02088-w ↗
35. 10.1002/aenm.20190168510.1002/aenm.201901685 ↗
36. 10.1016/j.joule.2019.11.00710.1016/j.joule.2019.11.007 ↗
37. 10.1002/aenm.20200294010.1002/aenm.202002940 ↗
38. 10.1021/acs.chemmater.6b0394410.1021/acs.chemmater.6b03944 ↗
39. 10.1021/acsami.0c1337410.1021/acsami.0c13374 ↗
40. 10.1002/anie.20181402410.1002/anie.201814024 ↗
41. 10.1021/ja512117e10.1021/ja512117e ↗
42. 10.1021/acs.inorgchem.9b0123310.1021/acs.inorgchem.9b01233 ↗
43. 10.1021/acs.jpclett.8b0372810.1021/acs.jpclett.8b03728 ↗
44. 10.1039/D1NR01281A10.1039/D1NR01281A ↗
45. 10.1021/nl501838y10.1021/nl501838y ↗
46. 10.1038/nenergy.2016.8110.1038/nenergy.2016.81 ↗
47. 10.1021/acsnano.7b0433210.1021/acsnano.7b04332 ↗
48. 10.1021/ja413224610.1021/ja4132246 ↗
49. 10.1021/acs.nanolett.6b0517710.1021/acs.nanolett.6b05177 ↗
50. 10.1021/j100072a02310.1021/j100072a023 ↗
51. 10.1038/s41467-020-15077-310.1038/s41467-020-15077-3 ↗
52. 10.1002/cssc.20160077110.1002/cssc.201600771 ↗
53. 10.1103/PhysRevApplied.10.04100110.1103/PhysRevApplied.10.041001 ↗
54. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
55. 10.1002/solr.20200005610.1002/solr.202000056 ↗
56. 10.1016/j.joule.2019.06.00510.1016/j.joule.2019.06.005 ↗