Structure–Property Relationships for Linear, Extended, and Branched Alkane Ammonium Iodide Derivatives as Interface Passivators for Narrow-Bandgap Lead–Tin Perovskite Solar Cells
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Interface passivation is crucial to reduce nonradiative recombination losses at the perovskite-electron transport layer interface and enhance the power conversion efficiency (PCE) of perovskite solar cells. Various molecules are known to result in a gain in open-circuit voltage ( V OC ). However, this gain is often associated with increased instability. Here, we investigate the interface passivation of a Cs 0.1 FA 0.6 MA 0.3 Pb 0.5 Sn 0.5 I 3 narrow-bandgap (1.26 eV) perovskite by ammonium iodide derivatives with multiple, primary, secondary, or tertiary ammonium iodide groups, connected via alkane linkers of different lengths to establish structure–property relationships. The impact of these passivators on interfacial recombination, charge extraction, and device stability is elucidated by tracking the quasi-Fermi level splitting (QFLS) of perovskite layers and perovskite/C 60 bilayers, together with the V OC of complete solar cell devices over one month. All tested passivators reduce the nonradiative recombination losses at the perovskite/C 60 interface, but the extent to which this translates into an improved photovoltaic performance strongly depends on the molecular structure. Short-chain primary diammonium passivators provide the most favorable balance between effective passivation and charge extraction, yielding QFLS values that closely match the device V OC . In contrast, extended and branched multiammonium passivators improve photovoltage stability but impede charge carrier extraction, leading to reduced fill factors (FF) and short-circuit current densities ( J SC ). Secondary ammonium terminal groups promote crystallite formation on the perovskite surface, which reduces the efficacy of passivation. Importantly, combining small with larger-sized passivators in a single layer enables simultaneous enhancement of QFLS, V OC, FF, and operational stability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Organic Electronics and Photovoltaics · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials to Optoelectronic Devices & Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands
Dutch Institute for Fundamental Energy Research, De Zaale 20, 5612 AJ Eindhoven, The Netherlands
Funding
European Research Council · HORIZON EUROPE European Innovation Council · Nederlandse Organisatie voor Wetenschappelijk Onderzoek
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