2023
DOI: 10.1016/j.joule.2023.04.009
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In situ epitaxial growth of blocking structure in mixed-halide wide-band-gap perovskites for efficient photovoltaics

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Cited by 17 publications
(9 citation statements)
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“…1,6–9 To break the efficiency limit of single-junction cells, perovskite tandem solar cells have been developed rapidly in the last several years. 10–22 Among them, all-perovskite tandem solar cells have promising prospects, thanks to their adjustable bandgaps ranging from 1.1 to 2.3 eV. So far, the highest efficiency achieved for all-perovskite tandem solar cells has been 28%, surpassing that of single-junction ones.…”
Section: Introductionmentioning
confidence: 99%
“…1,6–9 To break the efficiency limit of single-junction cells, perovskite tandem solar cells have been developed rapidly in the last several years. 10–22 Among them, all-perovskite tandem solar cells have promising prospects, thanks to their adjustable bandgaps ranging from 1.1 to 2.3 eV. So far, the highest efficiency achieved for all-perovskite tandem solar cells has been 28%, surpassing that of single-junction ones.…”
Section: Introductionmentioning
confidence: 99%
“…In this scenario, the iodide-rich regions will compromise the open-circuit voltage (V oc ) deficit and also the stability. [37] Phosphonic acid, with stronger binding strength to the oxide substrates, is currently the most preferred anchoring group of SAM-based HSLs. [38] To further enhance the illumination stability of these SAM-containing solar modules, Zhang et al innovatively introduced a cyanovinyl group near the phosphonic acid on a methoxyl-substituted triphenylamine terminal.…”
Section: Introductionmentioning
confidence: 99%
“…[10] For example, the halide segregation will produce a Br-rich perovskite region with high trap density and many deep-level defects, as well as an I-rich perovskite region that can become a charge recombination center and capture photogenerated carriers to prevent their transfer. [11] For mixed perovskites, the migration activation energy of X-site halide anions (0.1 eV) is lower than that of A-site cations (0.5 eV) and Bsite metal cations (0.8 eV). [12][13][14] Under illumination, due to the low electronegativity of iodine, I i − is easier to be trapped and oxidized by holes than Br i − , and rapid separation and aggregation occur.…”
Section: Introductionmentioning
confidence: 99%