Consistent Model of Ultrafast Energy Transfer in Peridinin Chlorophyll-a Protein Using Two-Dimensional Electronic Spectroscopy and Forster Theory

被引:10
作者
Toa, Zi S. D. [1 ]
deGolian, Mary H. [1 ]
Jumper, Chanelle C. [1 ]
Hiller, Roger G. [2 ]
Scholes, Gregory D. [1 ]
机构
[1] Princeton Univ, Dept Chem, Washington Rd, Princeton, NJ 08540 USA
[2] Macquarie Univ, Dept Biol, Fac Sci & Engn, Sydney, NSW 2109, Australia
关键词
INTRAMOLECULAR CHARGE-TRANSFER; S-2 1(1)B(U)(+) STATE; EXCITED-STATE; AMPHIDINIUM-CARTERAE; TRANSIENT ABSORPTION; TRANSFER PATHWAYS; CAROTENOIDS; DYNAMICS; COHERENT; COMPLEXES;
D O I
10.1021/acs.jpcb.9b04324
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solar light harvesting begins with electronic energy transfer in structurally complex light-harvesting antennae such as the peridinin chlorophyll-a protein from dinoflagellate algae. Peridinin chlorophyll-a protein is composed of a unique combination of chlorophylls sensitized by carotenoids in a 4:1 ratio, and ultrafast spectroscopic methods have previously been utilized in elucidating their energy-transfer pathways and timescales. However, due to overlapping signals from various chromophores and competing pathways and timescales, a consistent model of intraprotein electronic energy transfer has been elusive. Here, we used a broad-band two-dimensional electronic spectroscopy, which alleviates the spectral congestion by dispersing excitation and detection wavelengths. Interchromophoric couplings appeared as cross peaks in two-dimensional electronic spectra, and these spectral features were observed between the peridinin S-2 states and chlorophyll-a Q(x) and Q(y) states. In addition, the inherently high time and frequency resolutions of two-dimensional electronic spectroscopy enabled accurate determination of the ultrafast energy-transfer dynamics. Kinetic analysis near the peridinin S-1 excited-state absorption, which forms in 24 fs after optical excitation, reveals an ultrafast energy-transfer pathway from the peridinin S-2 state to the chlorophyll-a Q(x) state, a hitherto unconfirmed pathway critical for fast interchromophoric transfer. We propose a model of ultrafast peridinin chlorophyll-a protein photophysics that includes (1) a conical intersection between peridinin S-2 and S-1 states to explain both the ultrafast peridinin Si formation and the residual peridinin S-2 population for energy transfer to chlorophyll-a, and (2) computationally and experimentally derived peridinin S-2 site energies that support the observed ultrafast peridinin S-2 to chlorophyll-a Q(x) energy transfer.
引用
收藏
页码:6410 / 6420
页数:11
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