A Ga-doped SnO mesoporous contact for UV stable highly efficient perovskite solar cells
Increasing the stability of perovskite solar cells is a major challenge for commercialization. The highest efficiencies so far have been achieved in perovskite solar cells employing mesoporous TiO 2 (m-TiO 2 ). One of the major causes of performance loss in these m-TiO 2 -based perovskite solar cell...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018-01, Vol.6 (4), p.185-1857 |
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Zusammenfassung: | Increasing the stability of perovskite solar cells is a major challenge for commercialization. The highest efficiencies so far have been achieved in perovskite solar cells employing mesoporous TiO
2
(m-TiO
2
). One of the major causes of performance loss in these m-TiO
2
-based perovskite solar cells is induced by UV-radiation. This UV instability can be solved by replacing TiO
2
with SnO
2
; thus developing a mesoporous SnO
2
(m-SnO
2
) perovskite solar cell is a promising approach to maximise efficiency and stability. However, the performance of mesoporous SnO
2
(m-SnO
2
) perovskite solar cells has so far not been able to rival the performance of TiO
2
based perovskite solar cells. In this study, for the first time, high-efficiency m-SnO
2
perovskite solar cells are fabricated, by doping SnO
2
with gallium, yielding devices that can compete with TiO
2
based devices in terms of performance. We found that gallium doping severely decreases the trap state density in SnO
2
, leading to a lower recombination rate. This, in turn, leads to an increased open circuit potential and fill factor, yielding a stabilised power conversion efficiency of 16.4%. The importance of high-efficiency m-SnO
2
based perovskite solar cells is underlined by stability data, showing a marked increase in stability under full solar spectrum illumination.
Increasing the stability of perovskite solar cells is a major challenge for commercialization. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c7ta07663k |