4.8 Article

Hematite photoanodes with size-controlled nanoparticles for enhanced photoelectrochemical water oxidation

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 236, 期 -, 页码 117-124

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2018.04.073

关键词

Hematite photoanodes; Photoelectrochemical water splitting; Solar hydrogen production; Morphology directing agents; IMPS and PEIS

资金

  1. Science and Technology Development Fund (STDF, GERF III) [5064]
  2. Deanship of Scientific Research (DSR) at King Fand University of Petroleum & Minerals (KFUPM) [SR161020]

向作者/读者索取更多资源

The synthesis of hematite photoanodes with size-controlled nanoparticles is challenging due to the difficulty in finding the appropriate morphology-directing agents. In this paper, Ba2+ and Sr2+ ions were successfully employed to synthesize hematite photoanodes with size-controlled nanoparticles using a facile chemical bath deposition method. The synthesized electrodes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma-optical emission spectrometry (ICP-OES), (photo)electro-chemical impedance spectroscopy ((P)EIS), X-ray photoelectron spectroscopy (XPS) and intensity modulated photocurrent spectroscopy (IMPS) measurements. It was found that the average diameter of hematite nano particles is decreased by a factor of 13% and 35% by the addition of Ba2+ and Sr2+ ions into the chemical bath, respectively. In agreement with these results, the electroactive surface area of Ba- and Sr-modified hematite electrodes increased by 2.4 and 3.2 times, respectively, in comparison with that of bare hematite. The photo electro-chemical measurements under the standard illumination conditions revealed that the generated photo current at 1.23 V vs. RHE on Ba- and Sr-modified hematite photoanodes is 2.6 and 3 times higher than that of bare hematite, respectively. Moreover, the photocurrent onset potential for water oxidation on Ba- and Sr-modified hematite photoanodes was shifted cathodically by about 150 and 220 mV, respectively. Based on these results, a good correlation between the photocurrent and the electroactive surface area was observed at high bias potential (i.e., 1.23 V vs. RHE) evincing that the photocurrent enhancement can be readily attributed to the enhanced electroactive surface area. The cathodic shift in the photocurrent onset potential of water oxidation was elucidated, however, by the higher density of surface states and the higher rate constant of charge transfer as proven by the PEIS and IMPS measurements, respectively.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据