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Applied bias photon-to-current conversion efficiency of ZnO enhanced by hybridization with reduced graphene oxide

机译:与还原氧化石墨烯杂交提高了ZnO的应用偏置光子-电流转换效率

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摘要

The role of reduced graphene oxide (rGO) in the enhancement of photo-conversion efficiency of ZnO films for photoelectmchemical (PEC) water-splitting applications was analyzed.ZnO and rGO-hybridized ZnO (rGO/ZnO) films were prepared via a two-step electrochemical deposition method followed by annealing at 300 ℃ under argon gas flow.The physical,optical and electrochemical properties of the films were characterized to identify the effect of rGO-hybridization on the applied bias photon-to-current efficiency (ABPE) of ZnO.Scanning electron microscopy and X-ray diffraction indicated the formation of verticallyaligned,wurtzite-phase ZnO nanorods.Diffuse-reflectance UV-visible spectroscopy indicated that rGOhybridization was able to increase the light absorption range of the rGO/ZnO film.UPS analysis showed that hybridization with rGO increased the band gap of ZnO (3.56 eV) to 3.63 eV for rGO/ZnO sample,which may be attributed to the Burstein-Moss effect.Photoluminescence (PL) spectra disclosed that rGOhybridization suppressed electron-hole recombination due to crystal defects.Linear sweep voltammetry of the prepared thin films showed photocurrent density of 1.0 and 1.8 mA/cm2 for ZnO and rGO/ZnO at +0.7 V,which corresponded to an ABPE of 0.55% and 0.95%,respectively.Thus,this report highlighted the multi-faceted role of rGO-hybridization in the enhancement of ZnO photo-conversion efficiency.
机译:分析了氧化石墨烯(rGO)在提高ZnO薄膜在光电子化学(PEC)水分解应用中的光电转换效率中的作用。通过两步制备ZnO和rGO杂化的ZnO(rGO / ZnO)薄膜。分步电化学沉积方法,然后在氩气流下于300℃退火。表征膜的物理,光学和电化学性质,以鉴定rGO杂化对ZnO施加的偏置光子电流效率(ABPE)的影响扫描电子显微镜和X射线衍射表明形成了垂直排列的纤锌矿相ZnO纳米棒。漫反射紫外可见光谱表明rGO杂化能够增加rGO / ZnO薄膜的光吸收范围.UPS分析表明与rGO杂交使rGO / ZnO样品的ZnO(3.56 eV)带隙增加到3.63 eV,这可能归因于Burstein-Moss效应。线性扫描伏安法表明,ZnO和rGO / ZnO在+0.7 V时的光电流密度分别为1.0和1.8 mA / cm2,对应的ABPE为0.55%,线性结晶伏安法可抑制晶体缺陷引起的电子-空穴复合。因此,本报告强调了rGO杂交在提高ZnO光转换效率方面的多方面作用。

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  • 来源
    《天然气化学(英文版)》 |2017年第2期|302-308|共7页
  • 作者单位

    Nanotechnology and Catalysis Research Centre(NANOCAT), University of Malaya, 50603 Kuala Lumpur, Malaysia;

    Nanotechnology and Catalysis Research Centre(NANOCAT), University of Malaya, 50603 Kuala Lumpur, Malaysia;

    Nanotechnology and Catalysis Research Centre(NANOCAT), University of Malaya, 50603 Kuala Lumpur, Malaysia;

    Department of Industrial Chemistry, University of Messina, 98166 Messina, Italy;

    Department of Industrial Chemistry, University of Messina, 98166 Messina, Italy;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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