KCl-mediated defect passivation in vapor-deposited perovskites
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F25%3A00638046" target="_blank" >RIV/68378271:_____/25:00638046 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.1021/acsami.5c09426" target="_blank" >https://doi.org/10.1021/acsami.5c09426</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acsami.5c09426" target="_blank" >10.1021/acsami.5c09426</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
KCl-mediated defect passivation in vapor-deposited perovskites
Popis výsledku v původním jazyce
Perovskite-based solar cells (PSCs) have reached efficiencies comparable to those of commonly used silicon solar panels. Despite the promise of PSCs, their efficiency and commercial viability are currently restricted by three main factors: nonradiative charge recombinations on defects occurring within the light-absorbing layer and at its boundaries, limited reproducibility, and upscaling due to widely employed wet deposition methods. To address these issues, we investigated the defect passivation strategy by introducing potassium salt (KCl) during perovskite vapor deposition. We observed effective passivation of the defects upon KCl addition, manifested as an immediate and significant enhancement of the real-time photoluminescence (PL) intensity. The efficiency of passivation is related to the ionic nature of the potassium salt and its flux density. On the other hand, the perovskite’s crystallographic structure and texture, as observed from the grazing-incidence wide/small-angle X-ray scattering measurements, showed no significant changes due to KCl doping. Our work provides valuable insight into the possible passivation routes for the vapor-deposited perovskite layers, with implications for various chemical compositions or architectures.
Název v anglickém jazyce
KCl-mediated defect passivation in vapor-deposited perovskites
Popis výsledku anglicky
Perovskite-based solar cells (PSCs) have reached efficiencies comparable to those of commonly used silicon solar panels. Despite the promise of PSCs, their efficiency and commercial viability are currently restricted by three main factors: nonradiative charge recombinations on defects occurring within the light-absorbing layer and at its boundaries, limited reproducibility, and upscaling due to widely employed wet deposition methods. To address these issues, we investigated the defect passivation strategy by introducing potassium salt (KCl) during perovskite vapor deposition. We observed effective passivation of the defects upon KCl addition, manifested as an immediate and significant enhancement of the real-time photoluminescence (PL) intensity. The efficiency of passivation is related to the ionic nature of the potassium salt and its flux density. On the other hand, the perovskite’s crystallographic structure and texture, as observed from the grazing-incidence wide/small-angle X-ray scattering measurements, showed no significant changes due to KCl doping. Our work provides valuable insight into the possible passivation routes for the vapor-deposited perovskite layers, with implications for various chemical compositions or architectures.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10302 - Condensed matter physics (including formerly solid state physics, supercond.)
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ACS Applied Materials and Interfaces
ISSN
1944-8244
e-ISSN
1944-8252
Svazek periodika
17
Číslo periodika v rámci svazku
30
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
8
Strana od-do
43877-43884
Kód UT WoS článku
001532244000001
EID výsledku v databázi Scopus
2-s2.0-105012780755