%0 Journal Article
%T Enhancing Oxygen Evolution Electrocatalysis via the Intimate Hydroxide每Oxide Interface
%J -
%D 2018
%R https://doi.org/10.1021/acsnano.8b03141
%X The development of electrocatalysts with high activity and stability for oxygen evolution reaction (OER) is critically important, the one being regarded as the bottleneck process of overall water splitting. Herein, we fulfill significant OER improvement in both activity and stability by constructing a class of Ni(OH)2每CeO2 supported on carbon paper (NixCey@CP) with an intimate hydroxide (Ni(OH)2)每oxide (CeO2) interface. Such interface largely promotes the OER activity with a low overpotential of 220 mV at 10 mA cm每2 and a small Tafel slope of 81.9 mV dec每1 in 1 M KOH. X-ray photoelectron spectroscopy analysis shows that the intimate interface induced by the strong electronic interactions between Ni(OH)2 and CeO2 involves the modulation of binding strength between intermediates and catalysts, making a great contribution to the OER enhancement. Importantly, such intimate interface structures can be largely maintained even after a long-time stability test. We have further demonstrated that, when pairing the Ni4Ce1@CP after phosphorization (P每Ni4Ce1@CP), the Ni4Ce1@CP and P每Ni4Ce1@CP assembly is highly active and stable for overall water splitting with a low voltage of 1.68 V at 25 mA cm每2 and negligible stability delay over 30 h of continuous operation, which are much better than the commercial Ir/C and Pt/C
%U https://pubs.acs.org/doi/10.1021/acsnano.8b03141