Interlayer Expansion of Layered Cobalt Hydroxide Nanobelts to Highly Improve Oxygen Evolution Electrocatalysis

The water oxidation reaction is known to be energy-inefficient and generally considered as a major bottleneck for water splitting. Exploring electrocatalysts with high-efficiency and at low cost is vital to widespread utilization of this technology, but is still a big challenge. Here we report an effective strategy based on an expanding interlayer of layered structures to realize a great enhancement of the catalytic performance of the oxygen evolution reaction from water splitting. Well-defined nanobelts of layer structured cobalt benzoate hydroxide (Co(OH)(C6H5COO).H2O) are successfully prepared in terms of a simple hydrothermal process. Intercalation with benzoate ions induces the interlayer expansion of the cobalt hydroxide, which is useful for the accommodation of more electrolyte ions and favorable for their diffusion and transport. The as-prepared Co(OH)(C6H5COO)center dot H2O nanobelts need significantly smaller overpotential (similar to 0.36 V) to reach 10 mA center dot cm(-2) of current density compared with their Co(OH)2 (similar to 0.44 V) and Co3O4 (similar to 0.387 V) counterparts, and even favorably compare with most of the layered hydroxide-based electrocatalysts. Moreover, the Co (OH)(C6H5COO)center dot H2O nanobelts retain a much higher stability than the RuO2 reference in alkaline solution. This approach would be utilized to design and develop high-performance layered hydroxide-based electrocatalysts.