Abstract

This work examines the temperature dependence of electron transfer (ET) kinetics in solid-state films of mixed-valent states of monodisperse, small (<2 nm) Au monolayer protected clusters (MPCs). The mixed valent MPC films, coated on interdigitated array electrodes, are Au25(SR)18(0/1-), Au25(SR)18(1+/0), and Au144(SR)60(1+/0), where SR = hexanethiolate for Au144 and phenylethanethiolate for Au25. Near room temperature and for ca. 1:1 mol:mol mixed valencies, the bimolecular ET rate constants (assuming a cubic lattice model) are ~2 × 10(6) M(-1) s(-1) for Au25(SR)18(0/1-), ~3 × 10(5) M(-1) s(-1) for Au25(SR)18(1+/0), and ~1 × 10(8) M(-1) s(-1) for Au144(SR)60(1+/0). Their activation energy ET barriers are 0.38, 0.34, and 0.17 eV, respectively. At lowered temperatures (down to ca. 77 K), the thermally activated (Arrhenius) ET process dissipates revealing a tunneling mechanism in which the ET rates are independent of temperature but, among the different MPCs, fall in the same order of ET rate: Au144(+1/0) > Au25(0/1-) > Au25(1+/0).

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