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具有改善析氧性能的多复合纳米结构赤铁矿-二氧化钛光阳极:析氧催化剂的作用

Multicomposite Nanostructured Hematite-Titania Photoanodes with Improved Oxygen Evolution: The Role of the Oxygen Evolution Catalyst.

作者信息

Bärtsch Mario, Sarnowska Marta, Krysiak Olga, Willa Christoph, Huber Christian, Pillatsch Lex, Reinhard Sandra, Niederberger Markus

机构信息

Laboratory for Multifunctional Materials, Department of Materials, ETH Zurich, Vladimir-Prelog-Weg 5, 8093 Zurich, Switzerland.

Centre of New Technologies (CeNT), University of Warsaw, Żwirki i Wigury 93, 02-089 Warsaw, Poland.

出版信息

ACS Omega. 2017 Aug 15;2(8):4531-4539. doi: 10.1021/acsomega.7b00696. eCollection 2017 Aug 31.

Abstract

We present a sol-gel processed hematite-titania-based photoanode, which exhibits a photocurrent of up to 2.5 mA/cm at 1.23 V under simulated AM 1.5 G illumination (100 mW/cm) thanks to the addition of an amorphous cocatalyst with the nominal composition FeCrNiO . To unveil the role of the cocatalyst interconnected to the photoanode, we performed impedance measurements. According to the one order of magnitude higher value for the capacitance associated with surface states ( ) compared to the bare photoanode, the function of the catalyst-photoanode interface resembles that of a p-n-like junction. In addition, the charge transfer resistance associated with charge transfer processes from surface states ( ) was unchanged at potentials between 0.8 and 1.1 V after adding the cocatalyst, indicating that the catalyst has a negligible effect on the hole transport to the electrolyte. The understanding of the role of oxygen evolution catalysts (OECs) in conjunction with the photoanodes is particularly important for water splitting because most OECs are studied separately at considerably higher potentials compared to the potentials at which photoanode materials are operated.

摘要

我们展示了一种通过溶胶-凝胶工艺制备的基于赤铁矿-二氧化钛的光阳极,在模拟AM 1.5 G光照(100 mW/cm²)下,由于添加了标称组成为FeCrNiO的非晶态助催化剂,该光阳极在1.23 V时表现出高达2.5 mA/cm²的光电流。为了揭示与光阳极相连的助催化剂的作用,我们进行了阻抗测量。与裸光阳极相比,与表面态相关的电容值高一个数量级,催化剂-光阳极界面的功能类似于p-n结。此外,添加助催化剂后,在0.8至1.1 V的电位下,与表面态电荷转移过程相关的电荷转移电阻不变,这表明该催化剂对空穴传输到电解质的影响可忽略不计。对于水分解而言,理解析氧催化剂(OECs)与光阳极结合的作用尤为重要,因为与光阳极材料工作的电位相比,大多数OECs是在相当高的电位下单独研究的。

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