Atomic Layer Deposition of a Submonolayer Catalyst for the Enhanced Photoelectrochemical Performance of Water Oxidation with Hematite

被引:238
|
作者
Riha, Shannon C. [1 ,2 ]
Klahr, Benjamin M. [3 ]
Tyo, Eric C. [5 ]
Seifert, Soenke [4 ]
Vajda, Stefan [1 ,5 ,6 ]
Pellin, Michael J. [1 ,2 ]
Hamann, Thomas W. [3 ]
Martinson, Alex B. F. [1 ,2 ]
机构
[1] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
[2] Argonne Natl Lab, Argonne Northwestern Solar Energy Res ANSER Ctr, Argonne, IL 60439 USA
[3] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[4] Argonne Natl Lab, Xray Sci Div, Argonne, IL 60439 USA
[5] Yale Univ, Sch Engn & Appl Sci, Dept Chem & Environm Engn, New Haven, CT 06520 USA
[6] Argonne Natl Lab, Nanosci & Technol Div, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
hematite; Fe2O3; photoelectrocatalysis; water oxidation; electrochemical impedance spectroscopy; X-ray absorption spectroscopy; XANES; DRIVEN OXYGEN EVOLUTION; SOLAR-ENERGY CONVERSION; THIN-FILMS; SIZE; PHOTOANODES; KINETICS; SURFACE; DEHYDROGENATION; PHOTOLYSIS; HYDROGEN;
D O I
10.1021/nn305639z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hematite photoanodes were coated with an ultrathin cobalt oxide layer by atomic layer deposition (AID). The optimal coating-1 ALD cycle, which amounts to <1 monolayer of Co(OH)(2)/Co3O4-resulted in significantly enhanced photoelectrochemical water oxidation performance. A stable, 100-200 mV cathodic shift In the photocurrent onset potential was observed that is correlated to an order of magnitude reduction in the resistance to charge transfer at the Fe2O3/H2O Interface. Furthermore, the optical transparency of the ultrathin Co(OH)(2)/Co3O4 coating establishes it as a particularly advantageous treatment for nanostructured water oxidation photoanodes. The photocurrent of catalyst-coated nanostructured inverse opal scaffold hematite photoanodes reached 0.81 and 2.1 mA/cm(2) at 1.23 and 1.53 V, respectively.
引用
收藏
页码:2396 / 2405
页数:10
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