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Hydrogen Evolution from Pt/Ru-Coated p-Type WSe_2 Photocathodes

机译:从Pt / Ru涂层的p型WSe_2光电阴极析氢

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摘要

Crystalline p-type WSe_2 has been grown by a chemical vapor transport method. After deposition of noble metal catalysts, p-WSe_2 photocathodes exhibited thermody-namically based photoelectrode energy-conversion efficiencies of >7% for the hydrogen evolution reaction under mildly acidic conditions, and were stable under cathodic conditions for at least 2 h in acidic as well as in alkaline electrolytes. The open circuit potentials of the photoelectrodes in contact with the H~+/H_2 redox couple were very close to the bulk recombination/diffusion limit predicted from the Shockley diode equation. Only crystals with a prevalence of surface step edges exhibited a shift in flat-band potential as the pH was varied. Spectral response data indicated effective minority-carrier diffusion lengths of ~1 μm, which limited the attainable photocurrent densities in the samples to ~15 mA cm~(-2) under 100 mW cm~(-2) of Air Mass 1.5G illumination.
机译:结晶p型WSe_2已经通过化学气相传输法生长。沉积贵金属催化剂后,p-WSe_2光电阴极在温和的酸性条件下对氢的释放反应具有基于热力学的光电极能量转换效率> 7%,并且在酸性条件下也至少在阴极下稳定2 h如在碱性电解液中。与H〜+ / H_2氧化还原对接触的光电极的开路电势非常接近根据Shockley二极管方程预测的本体复合/扩散极限。随着pH值的变化,只有具有普遍的表面台阶边缘的晶体才显示出平带电势的变化。光谱响应数据表明有效的少数载流子扩散长度为〜1μm,这在100 mW cm〜(-2)的空气质量1.5G照明下将样品中可达到的光电流密度限制为〜15 mA cm〜(-2)。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第1期|223-231|共9页
  • 作者单位

    Division of Chemistry and Chemical Engineering and the Joint Center for Artificial Photosynthesis, California Institute of Technology, 1200 East California Blvd, Pasadena, California 91125, United States;

    Division of Chemistry and Chemical Engineering and the Joint Center for Artificial Photosynthesis, California Institute of Technology, 1200 East California Blvd, Pasadena, California 91125, United States;

    Division of Chemistry and Chemical Engineering and the Joint Center for Artificial Photosynthesis, California Institute of Technology, 1200 East California Blvd, Pasadena, California 91125, United States;

    Division of Chemistry and Chemical Engineering and the Joint Center for Artificial Photosynthesis, California Institute of Technology, 1200 East California Blvd, Pasadena, California 91125, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:12:28

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