Figure 1. (a) Schematic diagram representing electron transport in TiO₂ nanorods Vs. nanoparticle, (b) Cross-sectional FE-SEM images of PSC devices composed of TiO₂-NR and TiO₂-NP electrode, (c) Current-voltage spectrum of the two different photoelectrodes, and (d) Stability comparison of TiO_2-NR and TiO₂-NP based PSCs aged under ambient conditions (25^oC, 40 ~ 60% RH).

Indian Scientists have devised a new process for increasing the efficiency and stability of Titanium dioxide (TiO₂) nanorods based on Perovskite Solar Cells (PSC). It will help develop solar cells with stable light-harvesting active layer.

Perovskite solar cells have become commercially attractive because of the potential of achieving even higher efficiencies and very low production costs. However, the challenge lies in its short- and long-term stability.

Scientists led by Dr. V. Ganapathy from International Advanced Research Centre for Powder Metallurgy and New Materials, an autonomous institute of the Department of Science & Technology (DST), Government of India, have increased the efficiency and stability of Titanium dioxide (TiO₂) nanorods based Perovskite Solar Cells (PSC) by varying the length and porosity of the TiO₂-Nanorods. They did this by establishing a correlation between the lengths of the TiO₂-NR and the porosity of the electrode for the ambient processed PSCs.

The team explains that porosity of the electrode plays a vital role in perovskite infiltration and sensitization. The inter-pore distance between the two TiO₂ nanorods determines the photo-electrode’s porosity, and the porosity varies as the growth of the nanorod length increases.

“In this work, we had precise control over the length, porosity, and morphology of the TiO₂-NR from compact film to nanostructured film.”

The team controlled nanostructures of the TiO₂-NR by varying the concentration of the titania precursor and the growth time. The power conversion efficiency for nanorod-based PSCs was enhanced with variation in the length and porosity of the TiO₂-NR. The interspacing between the TiO₂-NR facilitated deep infiltration of the perovskite during the spin coating and is locally confined to the surface of the TiO₂-NR. Due to the large pores present in the TiO₂-NR photoelectrode, infiltration of small molecular HTM was also enhanced. The present work was published in the ‘Journal of Alloys and Compounds’,

The PSCs prepared with 350nm TiO₂-NR exhibited better efficiency when compared with the conventional NP-TiO₂. The similar thickness of NP-TiO₂ based device exhibited less photocurrent value than NR-TiO₂, which was attributed to the dense packing of 20nm TiO₂ particles inhibiting the loading of perovskite. The high crystallinity of the TiO₂-NR provided a low resistance to the flow of electrons in the Electron transport layer (ETL).

In the current work, apart from high efficiency, the crystalline structure of ETL also significantly influenced the stability of PSCs.

“The decomposition of perovskite absorber is a critical factor behind the performance degradation of PSCs. Given the similar nature of perovskite, enhanced stability of TiO₂-NR PSC is attributed to slow ion migration across thermodynamically stable rutile TiO₂-NR/MAPbI₃ interface,” added Dr. V. Ganapathy.

Publication Link: doi.org/10.1016/j.jallcom.2021.161061

For more details, Dr. V. Ganapathy, Scientist ([email protected]), can be contacted.