RESUMO
Recent multicolor photon-echo experiments revealed a long-lasting quantum coherence between excitations on the donor and acceptor in photosynthetic systems. Identifying the origin of the quantum coherence is essential to fully understand photosynthesis. Here we present a generic model in which a strong intermolecular steric restoring force in densely packed pigment-protein complexes results in a spatial correlation in conformational (static) variations of chromophores, which in turn induces an effective coupling between high-frequency (dynamic) fluctuations in donor and acceptor. The spatially correlated static and dynamic fluctuations provide a favorable environment to maintain quantum coherence, which can consistently explain the photon-echo measurements.
Assuntos
Fotossíntese , Benzeno/química , Cor , Simulação por Computador , Cinética , Luz , Conformação Molecular , Fótons , Teoria Quântica , TermodinâmicaRESUMO
We propose core-shell InP-CdS and InP-ZnTe nanorods as photoelectrodes in the efficient photoelectrochemical hydrogen production. On the basis of our systematic study using strain-dependent k.p theory, we find that in these heterostructures both energies and wave function distributions of electrons and holes can be favorably tailored to a considerable extent by exploiting the interplay between quantum confinement and strain. Consequently, these core-shell nanorods with proper dimensions (height, core radius, and shell thickness) can simultaneously satisfy all criteria for effective photoelectrodes in solar-based hydrogen production.