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Photoelectrochemical Activity of CdS/CdSe-deposited onto TiO_2 Photoanodes: Comparing Performance with vs. without Sacrificial Reagents

机译:CDS / CDSE的光电化学活性沉积在TiO_2 Photoanodes上:与VS.的性能与没有牺牲试剂相比

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The photocurrent density of CdS/CdSe-modified TiO_2 photoanodes measured under standard test conditions were 0.94 mAcm~(-2) and 7.4 mAcm~(-2) at 1.23 V_(RHE) using 1 M NaOH electrolyte (no reagents) and Na_2S/Na_2SO_3-added electrolyte (with reagents), respectively. The actual current contribution in the case of the aqueous alkaline electrolyte was due to water oxidation while the 8-fold photocurrent enhancement using the latter electrolyte was due to sulfite oxidation. A maximum Solar-To-Hydrogen (STH) efficiency of 0.71% and water splitting efficiency of 12.4% at 1.23 V_(RHE) were determined for the photoelectrochemical cell. The incident photon-to-current conversion efficiency spectrum measured for the photoanode revealed that the current conversion efficiency is lower (≤17%) when absorption occurs solely from the external CdSe layers, indicating higher recombination possibly due to unsaturated localized trap states and interfacial recombination during charge transport in the intermediate CdS layer. The photocurrent and onset potential for the CdS/CdSe-modified Li:TiO_2 photoanodes were found to improve under acidic conditions, showing a slightly increased PEC activity and faster reaction kinetics.
机译:在标准试验条件下测量的CDS / CDSE改性TiO_2光电码的光电流密度为1.23V_(rHE)的0.94mcm〜(-2)和7.4mMm〜(-2),使用1M NaOH电解质(无试剂)和Na_2s / Na_2SO_3-添加电解质(用试剂)。在碱性电解质水溶液的情况下的实际电流贡献是由于水氧化,而使用后一电解质的8倍光电流增强是由于亚硫酸盐氧化。为光电化学电池测定最大太阳能 - 氢气(STH)效率为0.71%,水分裂效率为1.23 V_(rHE)。测量的光电码的入射光子到电流转换效率谱显示,当吸收仅来自外部Cdse层时,当前转化效率较低(≤17%),表明由于不饱和局部捕集状态和界面重组可能是较高的重组在中间CD层中的电荷传输期间。 CDS / CDSE改性的Li:TiO_2光电池的光电流和发病电位在酸性条件下改善,显示出略微增加的PEC活性和更快的反应动力学。

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