Recombination reduction on lead halide perovskite solar cells based on low temperature synthesized hierarchical TiO2 nanorods. Issue 12 (30th November 2015)

• Record Type: Journal Article
• Authors: Jaramillo-Quintero, Oscar A.; Solís de la Fuente, Mauricio; Sanchez, Rafael S.; Recalde, Ileana B.; Juarez-Perez, Emilio J.; Rincón, Marina E.; Mora-Seró, Iván
• Is Part Of: Nanoscale. Volume 8:Issue 12(2016)
• Page Start: 6271
• Page End: 6277
• Publication Date: 2015-11-30
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c5nr06692a
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Hierarchical TiO2 nanorods produced at low temperature are effective selective contacts for perovskite solar cells due to reduced recombination. Abstract : Intensive research on the electron transport material (ETM) has been pursued to improve the efficiency of perovskite solar cells (PSCs) and decrease their cost. More importantly, the role of the ETM layer is not yet fully understood, and research on new device architectures is still needed. Here, we report the use of three-dimensional (3D) TiO2 with a hierarchical architecture based on rutile nanorods (NR) as photoanode material for PSCs. The proposed hierarchical nanorod (HNR) films were synthesized by a two-step low temperature (180 °C) hydrothermal method, and consist of TiO2 nanorod trunks with optimal lengths of 540 nm and TiO2 nanobranches with lengths of 45 nm. Different device configurations were fabricated with TiO2 structures (compact layer, NR and HNR) and CH3 NH3 PbI3, using different synthetic routes, as the active material. PSCs based on HNR-CH3 NH3 PbI3 achieved the highest power conversion efficiency compared to PSCs with other TiO2 structures. This result can be ascribed mainly to lower charge recombination as determined by impedance spectroscopy. Furthermore, we have observed that the CH3 NH3 PbI3 perovskite deposited by the two-step route shows higher efficiency, surface coverage and infiltration within the structure of 3D HNR than the one-step CH3 NH3 PbI3− x Cl x perovskite.