In this study, we propose a strategy to optimize the OER catalytic performance by precisely controlling the graphitization degree of the carbon-coating structure. The resulting catalyst exhibits excellent electrocatalytic activity with overpotent...
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Homogeneous Electrocatalytic Oxygen Reduction Reaction by a Versatile Polyoxometalate in an Aqueous Solution
Von Wiley-VCH zur Verfügung gestellt
In this work, we have explored a well-known water-soluble versatile polyoxometalate, Na6[V10O28]∙18H2O (1), for electrocatalytic homogeneous oxygen reduction reaction (ORR). Both RDE and RRDE experiments evident that compound 1 is actually involved in a two-electron reaction mixed with a four-electron reaction. Compound 1 exhibits remarkable stability in solution, remaining intact without decomposition/electrodeposition during electrocatalysis.
Abstract
The electrochemical production of H2O2 via a two-electron (2e−) oxygen reduction reaction (ORR) presents a compelling alternative to the traditional anthraquinone oxidation process used in industry, as it deals with limited H2O2 generation. This work describes the first paradigm of a polyoxometalate (POM) compound, Na6V10O28·18H2O (1), that per se exhibits aqueous homogeneous electrocatalytic oxygen reduction reaction (ORR). Compound 1 is not only a well-known and versatile POM compound but has also been extensively studied as far as its biological activities are concerned. However, it was never known that it has the ability to perform electrocatalytic ORR. In literature, a limited number of studies exist regarding POM-based materials that have been immobilized within various nanomaterials and employed as heterogeneous electrocatalysts for the ORR. Compound 1 demonstrates remarkable electrochemical stability in solution, as confirmed by a prolonged (10-hour) constant potential electrolysis. Throughout this extended electrolysis, compound 1 maintains its integrity without undergoing decomposition or electrodeposition, which has been rigorously verified through various spectroscopic and microscopic analyses. The K-L plot derived from the RDE experiment reveals that the number of electrons transferred for this ORR is 2.7 (at a potential of −0.5 V vs. NHE). The use of rotating ring-disc electrode (RRDE) experiments and spectrophotometry techniques have confirmed the electrochemical generation of H2O2. Compound 1 is involved in a two-electron transfer reaction mixed with a four-electron transfer reaction, generating 53% H2O2 by two-electron oxygen reduction.
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