Identifying Complexing Agents for the Selective Binding of Pb2+ Released During Perovskite Solar Cell Degradation
Tia Ansell a, Rhys Charles a, Rodrigo Garcia-Rodriguez a, Matthew Davies a b
a SPECIFIC IKC, Faculty of Science and Engineering, Swansea University, United Kingdom
b University of KwaZulu-Natal, School of Chemistry and Physics, Durban, South Africa
Proceedings of MATSUS Spring 2026 Conference (MATSUSSpring26)
G3 Stability Challenges and Solutions in metal halide Perovskites materials
Barcelona, Spain, 2026 March 23rd - 27th
Organizers: Andres Fabian Gualdron Reyes, Sofia Masi and Teresa S. Ripolles
Poster, Tia Ansell, 953
Publication date: 15th December 2025

Perovskite solar cells (PSCs) are an exciting, emerging photovoltaic technology showing promise for circular economy applications and contributing to net-zero targets. [1] Currently, PSCs demonstrate power conversion efficiencies up to 27.3 %, aided by a high absorption coefficient and ideal bandgap. [2-3] However, exposure to moisture, oxygen, heat or light decomposes the Pb-containing perovskite layer into water-soluble lead salts, Pb2+. These species may leach into the environment when modules are damaged during use or end-of-life processing. [4-5] This leads to harmful accumulation in our biosphere, ultimately impacting human health. [6] To mitigate this, colourimetric methods were explored to assess dyes that selectively bind Pb², enabling early detection of PSC degradation and prevention of lead release. Metal–ligand interactions were observed using UV–Vis absorbance alongside visual colour observations to evaluate binding behaviour and complex strength. By binding Pb² as it forms, these dyes support sequestration while simultaneously offering a visual indication of degradation. This results in an approach that aims to reduce environmental emissions and support real‑time monitoring of PSC stability.

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