Probing the Stability of Perovskite Solar Cell Under Working Condition Through an Ultra-Thin Silver Electrode: Beyond the Halide Ion Diffusion and Metal Diffusion

Abstract

Perovskite photovoltaic devices (PPDs) with an excellent optoelectronic performance have intrigued mushrooming research interests among various fields, and the undesirable intrinsic stability of halide perovskite materials still remains a severe constraint for their practical application. Fortunately, the ambiguous and complicated incentives for the degradation process of PPDs under working condition can be directly reflected on the corrosion of silver electrode by halogens. Here, we propose a novel perspective for the evaluation on the long-term stability of PPDs via the time-dependent transverse resistance variation of the ultra-thin Ag electrode under diverse working conditions. Being anode or cathode, the stability of ultra-thin silver layer has been systematically investigated through adjusting the external operating conditions of devices, i.e. light illumination and bias voltage. Experimental results indicate that the gradual resistance increases of silver film can be attributed to the oxidation of I- existing on the top surface of perovskite layer by non-equilibrium holes generated from light illumination or electrical injection for producing corrosive I2 gas, which will diffuse through the carrier transporting layer and attack the thin silver layer. The interaction probability of I- and non-equilibrium holes at the interface plays a critical role on the generation of I2 gas and resistance variation of the top thin silver electrode. The stability study of electrode indicator will shed light on the ambiguous degradation mechanisms of PPD under working condition, paving a path for conquering the fatal problems of the practical application.

Keywords: Perovskite solar cell, Metal electrode, stability, Ion migration.