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High efficient noble metal free Zn(O,S) nanoparticles for hydrogen evolution

机译:无氢的高效无贵金属Zn(O,S)纳米颗粒

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摘要

Noble metal-free zinc oxysulfide (Zn(O,S)) nanoparticles for H-2 evolution had been facilely synthesized by a low-cost chemical reaction at low process temperature of 70-90 degrees C with zinc acetate dihydrate as the zinc source and different amounts of thioacetamide as the sulfur precursor. The as-prepared Zn(O,S) had a nano crystallite size of 3-10 nm and formed aggregates. Low temperature process has led to the difficulty in forming well crystalline nanoparticles, therefore the ionic bonding is weaker as compared to the high temperature one. Due to the entropy-controlled reaction, Zn(O,S) with different compositions, phases, and bandgaps was formed and proposed to have a three-dimensional multibandgap-quantum-well (3D MQW) band structure, as supported by the selected area electron diffraction of high resolution transmission electron microscopy. Photo reduction of Cr6+ was initially performed for our materials selection. The photocatalytic hydrogen evolution reaction (HER) of Zn(O,S) in different kinds of solutions under low power UV lamps (the intensity is 0.088 mW/cm(2) or approximately 1/40 times UV light intensity of sunlight) was executed. A high efficient hydrogen evolution rate of 213 mu mol/g h watt was achieved by considering the input light power. The active surface oxygen anion-involved photocatalytic mechanism for HER is proposed, which was derived from the reversible change in Zn(O,S) color and the results from HER reactions in different solutions. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过廉价的化学反应,在70-90摄氏度的低工艺温度下,以二水合乙酸锌为锌源,通过低成本的化学反应,轻松合成了H-2生成的无贵金属的氧硫化锌(Zn(O,S))纳米粒子。不同量的硫代乙酰胺作为硫的前体。所制备的Zn(O,S)具有3-10nm的纳米微晶尺寸并形成聚集体。低温过程导致难以形成结晶良好的纳米粒子,因此与高温粒子相比,离子键较弱。由于受熵控制的反应,形成了具有不同组成,相和带隙的Zn(O,S),并建议其具有三维多带隙量子阱(3D MQW)的能带结构,受所选区域的支持高分辨率透射电子显微镜的电子衍射。 Cr6 +的光还原最初是为我们的材料选择而进行的。在低功率紫外线灯(强度为0.088 mW / cm(2)或日光紫外线强度的1/40倍)下,在不同溶液中进行Zn(O,S)的光催化氢释放反应(HER)。 。考虑到输入光功率,可以获得213μmol / g h瓦特的高效氢析出速率。提出了活性表面氧阴离子参与的HER的光催化机理,这是由Zn(O,S)颜色的可逆变化和HER在不同溶液中反应的结果得出的。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2017年第9期|5638-5648|共11页
  • 作者单位

    Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43 Sec 4,Keelung Rd, Taipei 10607, Taiwan;

    Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43 Sec 4,Keelung Rd, Taipei 10607, Taiwan;

    Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43 Sec 4,Keelung Rd, Taipei 10607, Taiwan;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    ZnOS; Hydrogen evolution; Photocatalyst;

    机译:ZnOS;氢析出;光催化剂;

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