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Cobalt Iron-Phosphorus Synthesized by Electrodeposition as Highly Active and Stable Bifunctional Catalyst for Full Water Splitting
27
Citations
21
References
2018
Year
Materials ScienceHighly ActiveChemical EngineeringFull Water SplittingEngineeringWater ElectrolysisSurface ElectrochemistryStable Bifunctional CatalystCatalysisChemistrySustainable Energy ConversionElectrochemical ProcessWater SplittingElectrode Reaction MechanismElectrochemistryCobalt Iron-phosphorus SynthesizedElectrochemical Water Splitting
Electrochemical water splitting is a promising method for sustainable energy conversion without environmental contamination. Developing active, stable, and low-cost electrocatalysts is important for practical applications with requirements such as scalability and durability. Herein, an efficient method for the electrodeposition of high-activity cobalt iron-phosphorus (CoxFe1-x-P) films as bi-functional electrocatalysts is presented. For films with a cobalt/iron atomic ratio of 1.07, the electrodeposited CoxFe1-x-P films showed outstanding electrocatalytic performance for both the H2 and O2 evolution reactions (HER and OER, respectively). In the HER, the overpotential and Tafel slope of the CoxFe1-x-P film on the copper plate were 169 mV at 10 mA/cm2 and 56.9 mV/dec, respectively. In the case of the OER, the CoxFe1-x-P film on dendritic copper exhibited superior performance with an overpotential of 290 mV and a Tafel slope of 39.2 mV/dec. In the two-electrode system consisting of CoxFe1-x-P film on the copper plate without (HER) and with dendritic copper (OER) for full water splitting, the electrodes exhibited a low overpotential of 1.64 V at 10 mA/cm2 and excellent long-term stability over several days under alkaline conditions.
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