Experimental evidence shows quantum interference affects localization in disordered graphene, suggesting novel thermoelectric properties.
We report direct experimental evidence for Anderson localization driven by quantum interference in disordered single-layer graphene induced via controlled Ar⁺ ion irradiation. By systematically introducing defects and quantifying the disorder using the Raman ID/IG ratio, we map the interdefect distance LD and uncover a critical localization threshold near LD* ≈ 20 nm, where multiple transport and spectroscopic signatures converge. Time-resolved reflectivity measurements reveal a nonmonotonic dependence of the carrier relaxation times τ₁,₂, peaking at LD*, indicating the emergence of spatially localized states. Tight-binding simulations confirm this threshold as the crossover between delocalized and exponentially localized regimes, satisfying the Ioffe-Regel condition kF l ≈ 1. Electrical resistivity increases exponentially below LD*, while Seebeck coefficients saturate, consistent with hopping-dominated transport. Notably, the power factor S²/ρ and the thermoelectric figure of merit zT exhibit pronounced maxima near LD*, corroborating theoretical predictions that localization can enhance thermoelectric performance by introducing sharp energy filtering at mobility edges. While graphene's intrinsic zT remains low due to high thermal conductivity, these results establish graphene as a model system for probing disorder-driven transport, offering the most direct experimental validation to date of localization-enhanced thermopower in two-dimensional Dirac systems.
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Francis et al. (2026) studied this question.
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