Engineering a chiral heterojunction enhances detection sensitivity of poly(vinyl chloride) in environmental settings, indicating its potential in biosensing applications.
Efficient suppression of carrier recombination is crucial for enhancing the performance of photoelectrochemical (PEC) biosensors. Here, we engineered a chiral molecule-modified BiOI/ZIF-8 (BZ) heterojunction in which the carrier separation efficiency of the paper-based photoactive chip is precisely regulated through manipulation of interfacial spin states and the rational construction of electron-transport pathways. The chirality-induced spin selectivity effect of the chiral molecule forces photogenerated electrons into a parallel spin configuration, thereby blocking spin-allowed electron-hole recombination and prolonging carrier lifetimes. Magnetic conductive atomic force microscopy measurements further confirm that the chiral topology induces a pronounced spin polarization of up to 70.8% at room temperature. As a proof-of-concept application, a paper-based spin tunable photoelectrochemical (μ-PEC) sensor was developed based on a competitive binding strategy for highly sensitive and selective onsite detection of poly(vinyl chloride) (PVC), with a detection limit of 1.32 ng/mL. This study demonstrates that the tunability of the spin degree of freedom provides a powerful avenue for transcending the inherent limitations of conventional photoactive materials, opening up promising avenues for environmental monitoring, spin-regulated optoelectronics, and next-generation photoelectrochemical sensing platforms.
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Shan et al. (2026) studied this question.
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