Decoupling Feature Size and Functionality in Solution-Processed, Porous Hematite Electrodes for Solar Water Splitting

被引:287
作者
Brillet, Jeremie [1 ]
Gratzel, Michael [1 ]
Sivula, Kevin [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Photon Interfaces, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
关键词
Iron oxide; nanostructured electrodes; photoelectrochemical energy storage; sintering; confinement; mesoporous silica; THIN-FILMS; ALPHA-FE2O3; OXIDE; PHOTOOXIDATION; PHOTOELECTROCHEMISTRY; PHOTOANODE; DEPOSITION; FE2O3;
D O I
10.1021/nl102708c
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
We introduce a simple solution-based strategy to decouple morphological and functional effects of annealing nanostructured, porous electrodes by encapsulation with a SiO2 confinement scaffold before high temperature treatment We demonstrate the effectiveness of this approach using porous hematite (alpha-Fe2O3) photoanodes applied for the storage of solar energy via water splitting and show that the feature size and electrode functionality due to dopant activation can be independently controlled This allows a significant increase in water oxidation photocurrent from 1 57 mA cm(-2) (in the control case) to 2 34 mA cm(-2) under standard illumination conditions in 1 M NaOH electrolyte the highest reported for a solution-processed hematite photoanode This increase is attributed to the improved quantum efficiency, especially with longer wavelength photons, due to a smaller particle size, which is afforded by our encapsulation strategy
引用
收藏
页码:4155 / 4160
页数:6
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