Reductive Contact and Dipolar Interface Engineering Enable Stable Flexible CsSnI3 Nanowire Photodetectors

Abstract

Lead-free tin-based halide perovskites are promising candidates for flexible and environmentally benign optoelectronic devices, yet their practical deployment is severely hindered by the rapid oxidation of Sn2+ to Sn4+ and the resulting performance degradation. Here, we report a flexible cesium tin triiodide (CsSnI3) nanowire photodetector that achieves remarkable stability and high near-infrared photoresponse through aluminium (Al) substrate contact engineering and dipolar interface modification. A 0.2 mm-thick anodized Al foil serves as the flexible substrate, where localized laser ablation exposes metallic Al regions that act as reductive sites, effectively suppressing Sn2+ oxidation during crystal growth. Simultaneously, a polar interlayer of 3-fluoro-2-nitroanisole is introduced to align energy levels and mitigate interfacial deprotonation, enhancing carrier extraction and environmental robustness.The resulting CsSnI3 nanowire device exhibits a responsivity of 0.39 A W⁻¹, a specific detectivity of 1.38 × 10^13 Jones, and a wide linear dynamic range of 156 dB under 850 nm illumination. Moreover, the device retains over 85% of its initial photocurrent after 60 days in ambient air and maintains 94% of its initial photocurrent after 1000 bending cycles, demonstrating excellent long-term operational and mechanical stability. This work establishes a synergistic "reductive contact + dipolar modification" paradigm for suppressing Sn2+ oxidation, offering a scalable route toward high-performance, durable, and flexible lead-free perovskite optoelectronics.

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Article information

Article type
Paper
Submitted
26 Jan 2026
Accepted
15 May 2026
First published
19 May 2026

Nanoscale, 2026, Accepted Manuscript

Reductive Contact and Dipolar Interface Engineering Enable Stable Flexible CsSnI3 Nanowire Photodetectors

L. Dai, W. Chen, Y. Xu, Q. Geng, G. Zhou, N. Chen and X. Li, Nanoscale, 2026, Accepted Manuscript , DOI: 10.1039/D6NR00349D

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