Atom-by-atom electrodeposition of single isolated cobalt oxide molecules and clusters for studying the oxygen evolution reaction

被引:81
作者
Jin, Zhaoyu [1 ]
Bard, Allen J. [1 ]
机构
[1] Univ Texas Austin, Dept Chem, Ctr Electrochem, Austin, TX 78712 USA
关键词
electrocatalysis; electrodeposition; oxygen evolution reaction; electrochemistry; single molecule; WATER OXIDATION; NUCLEATION; CATALYST; PHOSPHATE; METAL; ELECTROCATALYSTS; KINETICS; GROWTH; SIZE; IRON;
D O I
10.1073/pnas.2002168117
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report an electrodeposition protocol for preparing isolated cobalt oxide single molecules (Co1Ox) and clusters (ConOy) on a carbon fiber nanoelectrode. The as-prepared deposits are able to produce well-defined steady-state voltammograms for the oxygen evolution reaction (OER) in alkaline media, where the equivalent radius (r(d)) is estimated by the limiting current of hydroxide oxidation in accordance with the electrocatalytic amplification model. The size of isolated clusters obtained from the femtomolar Co2+ solution through an atom-by-atom technique can reach as small as 0.21 nm (r(d)) which is approximately the length of Co-O bond in cobalt oxide. Therefore, the deposit was close to that of a Co1Ox single molecule with only one cobalt ion, the minimum unit of the cobalt-based oxygen-evolving catalyst. Additionally, the size-dependent catalysis of the OER on ConOy deposits shows a faster relative rate on the smaller cluster in terms of the potential at a given current density, implying the single molecular catalyst shows a superior OER activity.
引用
收藏
页码:12651 / 12656
页数:6
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