Abstract
Redox hopping is the primary method of electron transport through redox-active metal-organic frameworks (MOFs). While redox hopping adequately supports the electrocatalytic application of MOFs, the fundamental understandings guiding the design of redox hopping MOFs remain nascent. In this study, we probe the rate of electron and hole transport through a singular MOF scaffold to determine whether the properties of the MOF promote the transport of one carrier over the other. A redox center, [Ru(II)(bpy)(2)(bpy-COOH)](2+), where bpy = 2,2'-bipyridine and bpy-COOH = 4-carboxy-2,2'-bipyridine, was anchored within NU-1000. The electron hopping coefficients (D(e)) and ion diffusion coefficients (D(i)) were calculated via chronoamperometry and application of the Scholz model. We found that electrons transport more rapidly than holes in the studied MOF. Interestingly, the correlation between D(e) and self-exchange rate built in previous research predicted reversely. The contradicting result indicates that spacing between the molecular moieties involved in a particular hopping process dominates the response.