Synergistic Solvent and Surface Engineering to Reduce VOC Loss in Tin Halide Perovskite Solar Cells
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Tin (Sn) halide perovskites, typically FASnI 3, resemble their lead (Pb)-based counterparts in optoelectronic properties but possess dissimilar crystallization kinetics leading to meager device performance. In this study, we fabricated FASn-halide perovskite solar cells (PSCs) with a high open-circuit voltage ( V OC ) of 1042 mV and a power conversion efficiency (PCE) of 15.48%, as verified by an independent photovoltaic lab. By employing a comprehensive solvent and surface engineering strategy, we enhanced crystal stability and grain size, reduced trap state density, and improved energy level alignment. This was achieved by introducing tetraethylammonium (TEA + ) cation at both surface and bulk grain boundaries, through the post-treatment of perovskite film with a preheated solution mixture of N, N -diethylformamide (DEF) and tetraethylammonium bromide (TEABr) in isopropanol (IPA). This approach also effectively suppressed the notorious Sn 2+ to Sn 4+ oxidation, resulting in reduced charge carrier trapping at grain boundaries. Moreover, the effectiveness and scalability of this strategy are validated with a 1.02 cm 2 active area device, achieving a high PCE of 12.21%. Our findings highlight the potential of Sn-halide PSCs to rival Pb-based PSCs in efficiency and stability, paving the way for more environmentally friendly, Pb-free alternatives.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Energy Conversion and Storage Lab, Department of Mechanical and Aerospace Engineering
Syracuse University
Department of Materials Science and Engineering City
University of Hong Kong
Department of Chemistry
Funding
Syracuse University
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