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Journal of materials chemistry. A, Materials for energy and sustainability, 2019, Vol.7 (35), p.239-2397
2019
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Autor(en) / Beteiligte
Titel
Structured crystallization for efficient all-inorganic perovskite solar cells with high phase stability
Ist Teil von
  • Journal of materials chemistry. A, Materials for energy and sustainability, 2019, Vol.7 (35), p.239-2397
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • All-inorganic perovskites suffer from a phase transition from a cubic α-phase to a tetragonal δ-phase in the ambient atmosphere, although they have the advantage of higher thermal stability. Here, we demonstrated that yttrium-induced perovskite crystallization results in significantly improved phase stability of perovskite even under humid air conditions. Yttrium in precursors was found to impede the crystal growth of perovskite film to stabilize the α-phase of a CsPbI 2 Br phase and was finally incorporated into the CsPbI 2 Br perovskite lattice. This structural crystallization process induced by yttrium incorporation gave rise to denser compact films with small grains and host lattice rearrangement by partial substitution for Pb. As a result, a 360-fold phase stability improvement was achieved in humid air with 65% RH compared with the reference film. The favorable electronic structure for efficient electron-hole dissociation and carrier transport to the cathode led to a much-enhanced power conversion efficiency (PCE) of 13.25% after yttrium incorporation compared with only 8.46% for the reference cells in humid air. Moreover, yttrium-incorporated perovskite solar cells (PSCs) without encapsulation exhibited superior long-term stability when stored in ambient air with 65% RH, showing nearly no degradation over 14 h. Yttrium incorporation enhanced the performance of CsPbI 2 Br perovskite solar cells and the phase stability was improved significantly.
Sprache
Englisch
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/c9ta05556h
Titel-ID: cdi_crossref_primary_10_1039_C9TA05556H

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