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Electrochemically Identified Ultrathin Water-Oxidation Catalyst in Neutral pH Solution Containing Ni2+ and Its Combination with Photoelectrode.


ABSTRACT: Water oxidation electrocatalyzed by Ni2+ under neutral conditions was investigated using various electrochemical analyses. The addition of Ni2+ in a phosphate-buffered solution catalyzed the oxidation of water, as confirmed by the detection of oxygen generation via scanning electrochemical microscopy. A combination of cyclic voltammetry, coulometric titration, and electrochemical quartz microbalance measurements identified the catalysis as heterogeneous and the catalyst as a Ni-based ultrathin (<4 nm) layer ("Ni-Pi"). Analysis of the potential- and pH-dependency of the titrated amount of charge revealed that the catalyst was deposited only under anodic polarization conditions and was removed under unpolarized conditions; the catalyst may be Ni(III) oxide, and its formation and oxidation appeared to be chemically irreversible. The diffusion-limited nature of water oxidation catalyzed by Ni2+ was closely related to the phosphate ions involved in the catalyst formation and the accompanying catalysis. Although the catalytic performance of Ni2+ alone was not remarkable, it exhibited a synergetic effect with BiVO4 for photoelectrochemical water oxidation, which can compete with Co-Pi-decorated BiVO4.

SUBMITTER: Cho SK 

PROVIDER: S-EPMC6641076 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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Electrochemically Identified Ultrathin Water-Oxidation Catalyst in Neutral pH Solution Containing Ni<sup>2+</sup> and Its Combination with Photoelectrode.

Cho Sung Ki SK   Chang Jinho J  

ACS omega 20170208 2


Water oxidation electrocatalyzed by Ni<sup>2+</sup> under neutral conditions was investigated using various electrochemical analyses. The addition of Ni<sup>2+</sup> in a phosphate-buffered solution catalyzed the oxidation of water, as confirmed by the detection of oxygen generation via scanning electrochemical microscopy. A combination of cyclic voltammetry, coulometric titration, and electrochemical quartz microbalance measurements identified the catalysis as heterogeneous and the catalyst as  ...[more]

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