期刊
ELECTROCHEMISTRY COMMUNICATIONS
卷 12, 期 5, 页码 632-635出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.elecom.2010.02.017
关键词
MOF; Voltammetry; Prussian blue; Reductive dissolution; Host guest electrochemistry; Water splitting; Sensor
资金
- Royal Society
- EPSRC [EP/H046305/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/H046305/1] Funding Source: researchfish
For the case of the commercially available metal-organic framework (MOF) structure Basolite (TM) F300 or Fe (BTC) with BTC = benzene-1,3,5-tricarboxylate, it is shown that the Fe(III/II) electrochemistry is dominated by reductive dissolution rather than ion insertion (which in marked contrast is dominating the behaviour of Fe(III/I) open framework processes in Prussian blues). Solid Fe(BTC) immobilised onto graphite or platinum working electrodes is investigated and it is shown that well-defined and reversible Fe(III/II) reduction responses occur only on platinum and in the presence of aqueous acid. The process is shown to follow a CE-type mechanism involving liberation of Fe(III) in acidic media, in particular for high concentrations of acid. Effective electrocatalysis for the oxidation of hydroxide to O-2 (anodic water splitting) is observed in alkaline aqueous media after initial cycling of the potential into the reduction potential zone. A mechanism based on a MOF-surface confined hydrous iron oxide film is proposed. (c) 2010 Elsevier B.V. All rights reserved.
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