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Demonstrates the interplay between interfacial dipoles and charge tunneling in inverted perovskite solar cells, indicating new design principles for enhancing efficiency.
High efficiencies of inverted perovskite solar cells that use self-assembled monolayers (SAMs) are closely tied to unresolved interfacial mechanisms. This study decouples the dual functions of carbazole-based SAMs featuring tailored alkyl chains. Kelvin probe force microscopy confirms that an interfacial dipole field, enhanced by longer chains, suppresses recombination and increases open-circuit voltage ( V OC ). In parallel, conductive atomic force microscopy shows that the alkyl chain itself serves as a tunneling barrier. Longer chains impede hole extraction, resulting in saturated tunneling current and a consequent decline in the maximum power point voltage ( V max ). This inherent trade-off defines the dual roles of SAMs: enhancing V OC through the dipole effect while mediating charge transfer via tunneling. An optimal balance is achieved with a four-carbon alkyl chain (4PACz), which combines efficient tunneling with strong passivation. Our findings provide a new design principle that co-optimization of dipole strength and tunneling probability is essential for developing high-performance SAMs.
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Wang et al. (2026) studied this question.
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