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This research advances the theoretical understanding of electron transfer in biological complexes by modeling non-Markovian dynamics and non-Condon coupling effects within a quantum-state diffusion framework. The study demonstrates how environmental memory and specific vibrational modes can cooperatively enhance transfer yields, offering refined mechanistic insights relevant to quantum biology and potential bio-inspired quantum device design.
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Non-Markovian and non-Condon vibrationally assisted electron transfer in an effective ligand--receptor complex

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arXiv:2602.06469v3 Announce Type: replace Abstract: We investigate vibrationally assisted electron transfer in an effective ligand--receptor complex using finite-temperature non-Markovian quantum-state diffusion with explicitly colored environmental noise. The model comprises donor and acceptor electronic states, an explicit bound-ligand vibrational mode, and a Gaussian protein--solvent bath. Linearization of a coordinate-dependent diabatic Hamiltonian yields two distinct system--environment interactions: diagonal coupling, which modulates the donor--acceptor energy gap, and off-diagonal non-Condon coupling, which modulates the electronic tunneling matrix element. In the rapidly equilibrating diagonal-bath limit, the model recovers the expected Marcus--Levich--Jortner vibronic-transfer behavior. Persistent environmental correlations instead generate non-exponential dynamics characterized by transient oscillations, back-transfer, and memory-dependent damping. Under matched weak-tunneling conditions, off-diagonal coupling opens a direct transition pathway and produces a larger finite-time acceptor population throughout the investigated parameter space. Because these dynamics do not generally support a unique kinetic rate, the enhancement is quantified using a time-averaged transfer yield. Comparisons with exact closed-system and commuting pure-dephasing limits validate the deterministic propagator and colored-noise construction, respectively, while the noncommuting dynamics are evaluated within a declared first-order finite-memory closure. These results identify ligand vibration, environmental memory, and non-Condon tunneling modulation as cooperating mechanisms that can dynamically regulate electron transfer in receptor-like environments, while maintaining a clear distinction between a mechanistic coarse-grained model and an atomistically parameterized biological complex.

Abstract:We investigate vibrationally assisted electron transfer in an effective ligand--receptor complex using finite-temperature non-Markovian quantum-state diffusion with explicitly colored environmental noise. The model comprises donor and acceptor electronic states, an explicit bound-ligand vibrational mode, and a Gaussian protein--solvent bath. Linearization of a coordinate-dependent diabatic Hamiltonian yields two distinct system--environment interactions: diagonal coupling, which modulates the donor--acceptor energy gap, and off-diagonal non-Condon coupling, which modulates the electronic tunneling matrix element. In the rapidly equilibrating diagonal-bath limit, the model recovers the expected Marcus--Levich--Jortner vibronic-transfer behavior. Persistent environmental correlations instead generate non-exponential dynamics characterized by transient oscillations, back-transfer, and memory-dependent damping. Under matched weak-tunneling conditions, off-diagonal coupling opens a direct transition pathway and produces a larger finite-time acceptor population throughout the investigated parameter space. Because these dynamics do not generally support a unique kinetic rate, the enhancement is quantified using a time-averaged transfer yield. Comparisons with exact closed-system and commuting pure-dephasing limits validate the deterministic propagator and colored-noise construction, respectively, while the noncommuting dynamics are evaluated within a declared first-order finite-memory closure. These results identify ligand vibration, environmental memory, and non-Condon tunneling modulation as cooperating mechanisms that can dynamically regulate electron transfer in receptor-like environments, while maintaining a clear distinction between a mechanistic coarse-grained model and an atomistically parameterized biological complex.

arXiv:2602.06469 [quant-ph]

(or arXiv:2602.06469v3 [quant-ph] for this version)

From: Muhammad Waqas Haseeb Mr. [view email] [v1] Fri, 6 Feb 2026 07:53:31 UTC (2,633 KB) [v2] Fri, 24 Apr 2026 20:13:24 UTC (2,630 KB) [v3] Sat, 26 Sep 2026 11:49:50 UTC (547 KB)

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