Conventional optoelectronic synapses predominantly emulate excitatory neuronal functions via positive photoconductivity, leaving the equally critical inhibitory signaling largely underexplored and vulnerable to visible‐light interference. Here, we unveil a negative photoconductivity (NPC) in the solar‐blind ultraviolet region, achieved at the shortest reported wavelength of 230 nm, in γ ‐Ga 2 O 3 quantum dots (QDs)/graphene heterojunctions. The mechanism originates from surface‐active oxygen vacancies (V O ) that enable reversible O 2 chemisorption; 230 nm illumination triggers hole‐O 2 − recombination, driving interfacial electron transfer that suppresses graphene conductance via a photo‐induced gating effect. This NPC physics delivers an ultrahigh responsivity of −8077 A/W and 279 s retention, emulating inhibitory plasticity (paired‐pulse depression, learning‐forgetting‐relearning). Harnessing the same nonlinear dynamics, we construct an in‐sensor reservoir computing system achieving 96% fingerprint recognition accuracy (91% under 30% noise) without preprocessing, far outperforming conventional visible‐light‐based schemes. Given that the ultrahigh specific surface area of the 0D QDs maximizes the fraction of surface‐exposed, chemically active V O defects for efficient interfacial charge exchange, this strategy establishes a 0D defect‐engineering paradigm for noise‐immune solar‐blind neuromorphic hardware.
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Lv et al. (2026) studied this question.
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