Lead‑free perovskite photodetectors now rival toxic lead‑based counterparts, opening pathways for sustainable, high‑performance imaging and sensing markets.
The emergence of lead‑free double perovskites has reshaped the optoelectronics landscape, yet scalable synthesis of high‑quality nanomaterials remained a bottleneck. In this study, low‑temperature injection colloidal methods combined with precise ligand selection produced quasi‑2D Cs2AgBiBr6 nanosheets with unprecedented lateral size and uniform thickness. This structural control not only enhances charge transport but also mitigates defect states that typically plague bulk perovskite films, positioning these nanosheets as a versatile platform for next‑generation devices.
When integrated into a transport‑layer‑free architecture, the nanosheets enabled photodetectors that surpass traditional benchmarks. Detectivity reached 1.15 × 10¹² Jones, while responsivity topped 121 mA/W, delivering on‑off ratios above 10⁴ and rise/decay times under one millisecond. Such performance metrics rival those of lead‑based perovskite detectors, but with the added advantage of environmental safety and reduced regulatory constraints. The rapid response is particularly valuable for applications ranging from high‑speed optical communication to biomedical imaging, where timing precision is critical.
Beyond immediate device metrics, the long‑term stability of these detectors underscores their commercial viability. Maintaining full photocurrent after 80 days of ambient exposure addresses a key reliability concern that has limited perovskite adoption. This durability, coupled with scalable colloidal production, suggests a clear pathway for mass‑manufacturing lead‑free photodetectors and potentially other optoelectronic components such as LEDs and solar cells. As industries prioritize sustainability, the demonstrated balance of performance, safety, and stability positions quasi‑2D Cs2AgBiBr6 nanosheets as a compelling alternative in the competitive photodetector market.
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