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. 2015 Oct 20;109(8):1735–1745. doi: 10.1016/j.bpj.2015.08.026

Figure 2.

Figure 2

Kinetics of the D-A triplet excitation transfer on a timescale Δtτtr(≪τdec) at ΔεDεIB > 0. The major contribution to the transfer process arises from the sequential route. If r−irf, then probability of the formation of intermediate state I (with the 1O2) can be rather large (a), whereas at r−irf the noted probability is small (b). The calculations are based on Eqs. 6–9, and Eqs. A2, B5, and A17 (see the Supporting Material) (at G0FI = ΔεIF −Δε) with T = 0.025 eV(≈290 K), ΔεD = −0.05 eV, ΔεA = −0.15 eV, Δε = 0.2 eV, λDλBI = 0.05 eV, λAλBF = 0.05 eV, λDAλFI = 0.06 eV, VO2,DVB,I = 5 × 10−4 eV, and VA,O2VF,B = 2 × 10−4 eV (a); and VO2,DVB,I = 1.5 × 10−4 eV and VA,O2VF,B = 5 × 10−3 eV (b).