We report the first spectroscopic demonstration of direct electron transfer between a gold nanoparticle and a surface-bound fluorophore induced by pulsed laser irradiation. Binding of pyrene thiol directly to the gold nanoparticle results in quenching of its singlet excited state. The suppression of S1−T1 intersystem crossing process as well as the formation of pyrene radical cation confirm the excited-state interaction between the metal nanoparticle and the surface-bound fluorophore. The charge separation is sustained for several microseconds before undergoing recombination.
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Ipe et al. (2001) studied this question.
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