Abstract
Cellulose films of variable thickness are electro-deposited from aqueous alkaline thiourea solution onto polished boron-doped diamond substrates in an anodic process. Films with “net-like” topography are formed and shown to consist of both cellulose-I and cellulose-II components. Properties of these films are investigated. When immersed in aqueous electrolyte solution, ion partitioning into the electro-deposited cellulose films occurs. The accumulation and release of two aqueous redox systems, Ru ( NH 3 ) 6 3 + / 2 + and methylviologen 2+/+, is reported. Relatively slow diffusion of these cations is observed within cellulose (approximately 5 orders of magnitude slower when compared to diffusion in aqueous media). For the methylviologen 2+/+ redox system partitioning leads to irreversibility in the voltammetric response and to the preferred formation of aggregates immobilized within the cellulose film.
Published Version
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