Broadband photodetectors with enhanced ultraviolet sensitivity are critical for applications including environmental monitoring and optical communications, yet achieving high performance at low operating voltages remains challenging. Hydrazopyridinium lead iodide (HPDLI), a two‐dimensional Dion–Jacobson (DJ) perovskite synthesized via in situ reduction of 4,4′‐azopyridine, achieves a bandgap of 2.13 eV, among the lowest reported for n = 1 lead halide systems, through an orthorhombic crystal structure with nearly linear Pb─I─Pb bonding (179.46°). This geometry maximizes metal‐halide orbital overlap, extending the broadband response toward the visible, with wavelength‐dependent absorption coefficients giving stronger sensitivity at shorter (deep‐UV) wavelengths. Lateral photodetectors exhibit 6 A/W responsivity, 1.01 × 10 12 Jones shot‐noise‐limited detectivity, and 2900% external quantum efficiency at 254 nm under a low 0.2 V bias. High‐gain response is consistent with trap‐mediated photoconductive mechanisms and a proposed type‐II band alignment, where hydrazopyridinium cations may extend carrier lifetimes. Millisecond rise/fall times (40/70 ms), preliminary stability screening (2000‐s cyclic and continuous‐illumination protocols, a 48 h/80% RH switching‐shape comparison), and retention of characteristic PXRD peak positions after 5 months of ambient storage support crystal engineering as a route to energy‐efficient UV‐to‐visible photodetection, though longer, quantitative operational testing remains necessary.
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Ajayakumar et al. (2026) studied this question.
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