Hybrid organic-inorganic halide perovskites have emerged at the forefront of solution-processable photovoltaic devices. Being the perovskite precursor mixture a complex equilibrium of species, it is very diffi cult to predict/control their interactions with different substrates, thus the fi nal fi lm properties and device performances. Here the wettability of CH 3 NH 3 PbI 3 (MAPbI 3 ) onto poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hole transporting layer is improved by exploiting the cooperative effect of graphene oxide (GO) and glucose inclusion. The glucose, in addition, triggers the reduction of GO, enhancing the conductivity of the PEDOT:PSS+GO+glucose based nanocomposite. The relevance of this approach toward photovoltaic applications is demonstrated by fabricating a hysteresis-free MAPbI 3 solar cells displaying a ?37% improvement in power conversion effi ciency if compared to a device grown onto pristine PEDOT:PSS. Most importantly, VOC reaches values over 1.05 V that are among the highest ever reported for PEDOT:PSS p-i-n device architecture, suggesting minimal recombination losses, high hole-selectivity, and reduced trap density at the PEDOT:PSS along with optimized MAPbI 3 coverage.
Hybrid organic-inorganic halide perovskites have emerged at the forefront of solution-processable photovoltaic devices. Being the perovskite precursor mixture a complex equilibrium of species, it is very difficult to predict/control their interactions with different substrates, thus the final film properties and device performances. Here the wettability of CH3NH3PbI3 (MAPbI(3)) onto poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) hole transporting layer is improved by exploiting the cooperative effect of graphene oxide (GO) and glucose inclusion. The glucose, in addition, triggers the reduction of GO, enhancing the conductivity of the PEDOT:PSS+GO+glucose based nanocomposite. The relevance of this approach toward photovoltaic applications is demonstrated by fabricating a hysteresis-free MAPbI(3) solar cells displaying a approximate to 37% improvement in power conversion efficiency if compared to a device grown onto pristine PEDOT:PSS. Most importantly, V-OC reaches values over 1.05 V that are among the highest ever reported for PEDOT:PSS p-i-n device architecture, suggesting minimal recombination losses, high hole-selectivity, and reduced trap density at the PEDOT:PSS along with optimized MAPbI(3) coverage.
Cooperative Effect of GO and Glucose on PEDOT:PSS for High V-OC and Hysteresis-Free Solution-Processed Perovskite Solar Cells
Giuri Antonella;Colella Silvia;Kovtun Alessandro;Dell'Elce Simone;Treossi Emanuele;Liscio Andrea;Rizzo Aurora;Listorti Andrea
2016
Abstract
Hybrid organic-inorganic halide perovskites have emerged at the forefront of solution-processable photovoltaic devices. Being the perovskite precursor mixture a complex equilibrium of species, it is very difficult to predict/control their interactions with different substrates, thus the final film properties and device performances. Here the wettability of CH3NH3PbI3 (MAPbI(3)) onto poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) hole transporting layer is improved by exploiting the cooperative effect of graphene oxide (GO) and glucose inclusion. The glucose, in addition, triggers the reduction of GO, enhancing the conductivity of the PEDOT:PSS+GO+glucose based nanocomposite. The relevance of this approach toward photovoltaic applications is demonstrated by fabricating a hysteresis-free MAPbI(3) solar cells displaying a approximate to 37% improvement in power conversion efficiency if compared to a device grown onto pristine PEDOT:PSS. Most importantly, V-OC reaches values over 1.05 V that are among the highest ever reported for PEDOT:PSS p-i-n device architecture, suggesting minimal recombination losses, high hole-selectivity, and reduced trap density at the PEDOT:PSS along with optimized MAPbI(3) coverage.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.