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Nucleation of binary Cu-Se phases and electrochemical cementation mechanism on polycrystalline molybdenum thin films in Cu(II)-In(III)-Se(IV) acidic solutions

机译:二元Cu-SE相和电化学胶粘机制在Cu(II)-INSE(II) - 酸溶液中的多晶硅薄膜上的多晶钼薄膜

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The behavior of sputter deposited polycrystalline thin films of molybdenum covered glass plates, used as standard back contact for thin Cu(In, Ga)(S,Se){sub}2 solar cells is examined while in contact with acidic aqueous solutions containing Cu(II), In(III) and Se(IV) species at open circuit potential. These solutions are used for the electrodeposition of CuInSe{sub}2 thin films. An electrochemical investigation was carried out, in combination with SEM-FEG observations, Raman spectroscopy and XPS surface analysis. It is shown that molybdenum undergoes an electrochemical cementation reaction. Its potential increases with immersion time. Immediately after immersion, small nuclei appear on the surface, which then grow to form a quasi-continuous layer after 600s. The chemical composition of the layer evolves with immersion time. No indium is incorporated. CuSe phases are formed whose composition changes from Se/Cu>0.3 to a Se/Cu atomic ratio ~ 0.7. The final layer contains two phases, Umangite Cu{sub3Se{sub}2 and CuSe.
机译:钼覆盖玻璃板的溅射沉积多晶薄膜的行为,用作薄Cu(in,ga)(se)(se){sea} 2太阳能电池的标准后触点,同时与含Cu的酸性水溶液接触( II),在开路电位的(III)和SE(IV)中的物种。这些溶液用于Cuinse {Sub} 2薄膜的电沉积。进行电化学研究,结合SEM-FEG观察,拉曼光谱和XPS表面分析。结果表明,钼经历了电化学胶结反应。它的潜力随着浸入时间而增加。浸泡后立即,表面上出现小核,然后在600秒后生长以形成准连续层。层的化学成分随着浸入时间而发展。没有铟被纳入。形成蚕豆相,其组合物从SE / Cu> 0.3变为Se / Cu原子比〜0.7。最终层包含两个阶段,Umangite Cu {sub3se {sub} 2和cues。

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