Design of two-dimensional perovskite solar cells with superior efficiency and stability

ABSTRACT : Pervskite solar cells have attracted extensive attention from researchers worldwide due to their rapid development and efficiency. Nevertheless, stability is still an issue that limits the advance of this technology. In this work, we present the fabrication and characterization of two-dim...

Full description

Autores:
Ramírez Zora, Daniel Estiben
Jaramillo Isaza, Franklin
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/24968
Acceso en línea:
http://hdl.handle.net/10495/24968
https://revistas.udea.edu.co/index.php/ingenieria/article/view/344428
Palabra clave:
Estabilidad
Stability
Cationes
Cations
Energía solar
Solar energy
Perovskitas de haluro metal bidimensionales
Celdas solares
ationes orgánicos
http://aims.fao.org/aos/agrovoc/c_36930
http://aims.fao.org/aos/agrovoc/c_16169
http://aims.fao.org/aos/agrovoc/c_7222
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-sa/4.0/
Description
Summary:ABSTRACT : Pervskite solar cells have attracted extensive attention from researchers worldwide due to their rapid development and efficiency. Nevertheless, stability is still an issue that limits the advance of this technology. In this work, we present the fabrication and characterization of two-dimensional perovskites of the Ruddlesden-Popper’s family (A)2(MA)n−1PbnI3n+1 (three different A-site large cations were investigated: A=n-propylammonium, t-Butylammonium or Benzylammonium). The modulation of the large organic cations increased the band gap of the materials and improved moisture and thermal stability, making it possible to fabricate PSCs. Even though the organic interlayers intrinsically reduce the transport properties of the devices and therefore lower currents are obtained in the layered systems, a remarkable efficiency of 10.35% was obtained for (BUA)2(MA)2Pb3I10, with superior stability, and therefore, it was possible to retain 68% of its initial value after 1700 h for devices without encapsulation.