Electrochemical Water Oxidation Catalyzed by an In Situ Generated α-Co(OH)2 Film on Zeolite-Y Surface

2017 
The design and synthesis of an efficient and robust water-oxidation catalyst with inexpensive materials remains an important challenge in the context of artificial photosynthesis. Herein, a simple but unique technique is reported to in situ generate a thin-film of α-Co(OH)2 on the surface of zeolite-Y [hereafter referred to as Y-α-Co(OH)2] that acts as an efficient and stable catalyst for electrochemical water oxidation in alkaline medium. Catalyst Y-α-Co(OH)2 is so stable that it retains its catalytic activity even after 2000 cyclic voltammetric cycles of water oxidation. Expectedly, the chemical composition of α-Co(OH)2 on the surface of zeolite-Y remains same as that of parent Y-α-Co(OH)2 after 2000 electrocatalytic cycles. A Tafel slope as low as 59 mV decade−1 in 0.1 m KOH (pH 13) suggests faster oxygen evolution kinetics (overpotential=329 mV; turnover frequency=0.35 mol O2 (mol Co)−1 s−1 at 1 mA cm−2) than the existing α-Co(OH)2-based electrocatalysts operating in alkaline medium.
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