首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Enhanced Photoelectrochemical Water Oxidation on Nanostructured Hematite Photoanodes via p-CaFe2O4-Fe2O3 Heterojunction Formation
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Enhanced Photoelectrochemical Water Oxidation on Nanostructured Hematite Photoanodes via p-CaFe2O4-Fe2O3 Heterojunction Formation

机译:通过p-CaFe2O4 / n-Fe2O3异质结形成增强的纳米结构赤铁矿光阳极上的光电化学水氧化

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In this paper, nanostructured hematite p-CaFe2O4-Fe2O3 heterojunction photoanodes have been fabricated employing a facile template-less film processing technique by controlling the chemical bath. Anisotropic growth of a beta-FeOOH akaganeite film on FTO conductive glass from an aqueous FeCl3 solution containing CaCl2 followed by a two-step thermal annealing at 550 and 800 degrees C induces the formation of a p-CaFe2O4-Fe2O3 heterojunction. The structural, morphological, electronic states, and electrochemical characteristics of the films have been investigated by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, and impedance spectroscopy, respectively. The heterojunction photoanode showed 100% higher photocurrent response than that obtained using a bare hematite electrode under simulated 1-sun illumination (100 mW/cm(2)). The photocurrent enhancement is attributed to the enhanced charge carrier separation and the reduced resistance in the charge transfer across the electrode and the electrolyte as revealed by electrochemical impedance spectroscopy analysis. The modification of the p-CaFe2O4-Fe2O3 heterojunction photoanode with CoPi cocatalyst further facilitates the electron transfer at the electrode/electrolyte interface and thus enhances the photoelectrochemical water oxidation. Since cheap and abundant materials have been employed for the synthesis of the heterojunction photoanode via a simple route, the current results have great importance, both from a scientific and an economical point of view.
机译:在本文中,通过控制化学浴,采用简便的无模板薄膜加工技术,制备了纳米结构的赤铁矿p-CaFe2O4 / n-Fe2O3异质结光阳极。从含有CaCl2的FeCl3水溶液在FTO导电玻璃上各向异性生长β-FeOOH赤铁矿薄膜,然后在550和800摄氏度进行两步热退火,诱导了p-CaFe2O4 / n-Fe2O3异质结的形成。分别通过X射线衍射,扫描电子显微镜,X射线光电子能谱和阻抗谱研究了膜的结构,形态,电子态和电化学特性。异质结光电阳极比在模拟的1阳光照射下(100 mW / cm(2))使用裸露的赤铁矿电极获得的光电流响应高100%。光电流的增强归因于增强的电荷载流子分离和通过电极和电解质的电荷转移中降低的电阻,如通过电化学阻抗谱分析所揭示的。用CoPi助催化剂对p-CaFe2O4 / n-Fe2O3异质结光阳极进行改性,进一步促进了电子在电极/电解质界面处的转移,从而增强了光电化学水的氧化。由于已经通过简单的途径将廉价且丰富的材料用于异质结光电阳极的合成,从科学和经济的角度来看,当前的结果都具有重要意义。

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