Abstract
Inverted perovskite solar cells (PSCs) promise enhanced operating stability compared to their normal-structure counterparts1–3. To improve efficiency further, it is crucial to combine effective light management with low interfacial losses4,5. Here we develop a conformal self-assembled monolayer (SAM) as the hole-selective contact on light-managing textured substrates. Molecular dynamics simulations indicate cluster formation during phosphonic acid adsorption leads to incomplete SAM coverage. We devise a co-adsorbent strategy that disassembles high-order clusters, thus homogenizing the distribution of phosphonic acid molecules, thereby minimizing interfacial recombination and improving electronic structures. We report a lab-measured power-conversion efficiency (PCE) of 25.3% and a certified quasi-steady-state PCE of 24.8% for inverted PSCs, with a photocurrent approaching 95% of the Shockley-Queisser maximum. An encapsulated device having a PCE of 24.6% at room temperature retains 95% of its peak performance when stressed at 65°C and 50% relative humidity following >1000 hours of maximum power point tracking under 1-sun illumination. This represents one of the most stable PSCs subjected to accelerated ageing – achieved with a PCE surpassing 24%. The engineering of phosphonic acid adsorption on textured substrates offers a promising avenue for efficient and stable PSCs. It is also anticipated to benefit other optoelectronic devices that require light management.
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Supplementary information
Supplementary Information
This file contains Supplementary Notes 1-5, Supplementary Tables 1-3, and Supplementary References.
Reporting Summary
Supplementary Video 1
Classical MD simulations of 2PACz adsorption.
Supplementary Video 2
Classical MD simulations of 2PACz:3-MPA adsorption.
Supplementary Video 3
AIMD simulations of 2PACz-3-MPA adsorption.
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Park, S.M., Wei, M., Lempesis, N. et al. Low-loss contacts on textured substrates for inverted perovskite solar cells.
Nature (2023). https://doi.org/10.1038/s41586-023-06745-7
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Received: 28 June 2023
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Accepted: 12 October 2023
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Published: 23 October 2023
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DOI: https://doi.org/10.1038/s41586-023-06745-7
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