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Giant photovoltaic response in band engineered ferroelectric perovskite

Recently the solar energy, an inevitable part of green energy source, has become a mandatory topics in frontier research areas. In this respect, non-centrosymmetric ferroelectric perovskites with open circuit voltage (V(OC)) higher than the bandgap, gain tremendous importance as next generation phot...

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Detalles Bibliográficos
Autores principales: Pal, Subhajit, Swain, Atal Bihari, Biswas, Pranab Parimal, Murali, D., Pal, Arnab, Nanda, B. Ranjit K., Murugavel, Pattukkannu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964148/
https://www.ncbi.nlm.nih.gov/pubmed/29789634
http://dx.doi.org/10.1038/s41598-018-26205-x
Descripción
Sumario:Recently the solar energy, an inevitable part of green energy source, has become a mandatory topics in frontier research areas. In this respect, non-centrosymmetric ferroelectric perovskites with open circuit voltage (V(OC)) higher than the bandgap, gain tremendous importance as next generation photovoltaic materials. Here a non-toxic co-doped Ba(1−x)(Bi(0.5)Li(0.5))(x)TiO(3) ferroelectric system is designed where the dopants influence the band topology in order to enhance the photovoltaic effect. In particular, at the optimal doping concentration (x(opt) ~ 0.125) the sample reveals a remarkably high photogenerated field E(OC) = 320 V/cm (V(OC) = 16 V), highest ever reported in any bulk polycrystalline non-centrosymmetric systems. The band structure, examined through DFT calculations, suggests that the shift current mechanism is key to explain the large enhancement in photovoltaic effect in this family.