首页> 外文会议>Nanostructured materials and nanotechnology VI >PLASMA-ASSISTED CHEMICAL VAPOR DEPOSITION OF Fe:TIO_2 FILMS FOR PHOTOELECTROCHEMICAL HYDROGEN PRODUCTION
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PLASMA-ASSISTED CHEMICAL VAPOR DEPOSITION OF Fe:TIO_2 FILMS FOR PHOTOELECTROCHEMICAL HYDROGEN PRODUCTION

机译:Fe:Tio_2薄膜的等离子体辅助化学气相沉积法用于光电子制氢

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摘要

Fe-doped TiO_2 (Fe:TiO_2) thin films were deposited onto fluorine-doped tin oxide (FTO, SnO_2:F), substrates via plasma enhanced chemical vapor deposition (PE-CVD) using a stoichiometric mixture of iron pentacarbonyl (Fe(CO)_5) and titanium isopropoxide (Ti(OPr)_4) as precursors. The evolution of surface morphology with changing process parameters was studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM). UV-Visible spectral data showed a shift of the absorption edge towards the visible region and the band gap energy was found to gradually decrease with increasing dopant (Fe) concentration. Photoelectrochemical (PEC) measurements carried out on Fe:TiO_2 samples under 1 Sun illumination using 1M NaOH as electrolyte showed maximum photocurrent density and flatband potential of 1.26 mA/cm~2 and 0.68V/SCE, respectively at 5.0 at% Fe doping. Incident photon-to-electron conversion efficiency (IPCE) was found to increase from 0.75% to 4.0% upon increasing the dopant concentration upto 5.0 at%.
机译:掺杂铁的TiO_2(Fe:TiO_2)薄膜使用五羰基铁(Fe(CO)的化学计量混合物)通过等离子体增强化学气相沉积(PE-CVD)沉积在掺杂氟的氧化锡(FTO,SnO_2:F)的基板上)_5)和异丙醇钛(Ti(OPr)_4)作为前体。通过扫描电子显微镜(SEM)和原子力显微镜(AFM)研究了工艺参数变化时表面形态的演变。紫外可见光谱数据显示吸收边缘向可见光区域移动,并且发现带隙能量随掺杂剂(Fe)浓度的增加而逐渐降低。使用1M NaOH作为电解质在1:阳光照射下对Fe:TiO_2样品进行的光化学(PEC)测量显示,在5.0 at%的Fe掺杂下,最大光电流密度和平带电势分别为1.26 mA / cm〜2和0.68V / SCE。发现将掺杂剂浓度提高到5.0 at%时,入射光子-电子转换效率(IPCE)从0.75%增加到4.0%。

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  • 会议地点 Daytona Beach FL(US);Daytona Beach FL(US);Daytona Beach FL(US)
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    Chair of Inorganic and Materials Chemistry, Department of Chemistry University of Cologne, Greinstr. 6, Cologne D 50859, Germany;

    Chair of Inorganic and Materials Chemistry, Department of Chemistry University of Cologne, Greinstr. 6, Cologne D 50859, Germany;

    Chair of Inorganic and Materials Chemistry, Department of Chemistry University of Cologne, Greinstr. 6, Cologne D 50859, Germany;

    Department of Chemistry and Bioengineering, Tampere University of Technology P. O. Box 541, FI-33101 Tampere, Finland;

    Chair of Inorganic and Materials Chemistry, Department of Chemistry University of Cologne, Greinstr. 6, Cologne D 50859, Germany;

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