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首页> 外文期刊>Journal of materials science >Structural, optical, photocurrent and mechanism-induced photocatalytic properties of surface-modified ZnS thin films by chemical bath deposition
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Structural, optical, photocurrent and mechanism-induced photocatalytic properties of surface-modified ZnS thin films by chemical bath deposition

机译:化学浴沉积表面改性的ZnS薄膜的结构,光学,光电流和机理诱导的光催化性能

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摘要

ZnS thin films were prepared by chemical bath codeposition using ZnSO_4-ZnCl_2 or Zn(CH_3COO)_2-ZnCl_2 as zinc ion sources. The presence of SO_4~(2-) favors the heterogeneous growth of ZnS thin film. The coexistence of two zinc salts impedes the formation of homogeneous precipitation and improves the growth rate of ZnS film. XRD and HRTEM results show that all the samples exhibit the cubic structure. EDS analysis shows that Zn/S atom ratios from the codeposition are closer to 1:1 than those deposited from a single zinc salt, and ZnS thin films of S3 and S7 are very uniform without stirring. FTIR reveals that -NH_2 group as a surface modifier is adsorbed on the surface of ZnS nanoparticles. Raman spectra further reveal that S3, S4 and S7 form the ZnS films, and ZnO phase is present in short or middle range of the S6 nanocrystal, indicating that different amounts of zinc salts affect the structure of ZnS films significantly after three 2.5 h deposition cycles. The grain sizes determined by FESEM are inversely proportional to RMS determined by AFM. The band gap values of ZnS thin films agree well with the results of HRTEM. The photocurrent responses of different samples are similar, indicating that different amounts of zinc salts have little effect on the photocurrent of ZnS films. The photocatalytic performance of S6 and S8 is much better than that of S1-S5. S6 decomposes 65 % of methyl orange within 3 h, and its K value is 4.78 × 10~(-1) h~(-1). The photocatalytic performance is induced by the growth mechanism, which determines the grain size of ZnS thin film. The tendency of grain sizes of ZnS films agrees well with that of photocatalytic performance, especially under the clusters by clusters deposition.
机译:采用ZnSO_4-ZnCl_2或Zn(CH_3COO)_2-ZnCl_2作为锌离子源通过化学浴共沉积制备ZnS薄膜。 SO_4〜(2-)的存在有利于ZnS薄膜的异质生长。两种锌盐的共存阻碍了均匀沉淀的形成并提高了ZnS膜的生长速率。 XRD和HRTEM结果表明,所有样品均呈现立方结构。 EDS分析表明,与从单一锌盐沉积的锌/ S原子比相比,共沉积的Zn / S原子比更接近1:1,并且S3和S7的ZnS薄膜非常均匀,无需搅拌。 FTIR表明,作为表面改性剂的-NH_2基团被吸附在ZnS纳米颗粒的表面上。拉曼光谱进一步揭示了S3,S4和S7形成ZnS膜,并且ZnO相存在于S6纳米晶体的中短范围内,表明在三个2.5 h的沉积循环后,不同量的锌盐会显着影响ZnS膜的结构。 。 FESEM确定的晶粒尺寸与AFM确定的RMS成反比。 ZnS薄膜的带隙值与HRTEM结果吻合良好。不同样品的光电流响应是相似的,表明不同量的锌盐对ZnS薄膜的光电流影响很小。 S6和S8的光催化性能比S1-S5好得多。 S6在3 h内分解了65%的甲基橙,其K值为4.78×10〜(-1)h〜(-1)。光催化性能是由生长机理引起的,生长机理决定了ZnS薄膜的晶粒尺寸。 ZnS薄膜的晶粒尺寸趋势与光催化性能相吻合,特别是在团簇沉积的团簇下。

著录项

  • 来源
    《Journal of materials science》 |2017年第1期|28-42|共15页
  • 作者单位

    Jiangxi Key Laboratory of Surface Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China;

    High Level Engineering Research Center of Biopharmaceutical Molecules and Diagnostic Apparatuses, Jiangxi Provincial Colleges and Universities, Jiangxi Science and Technology Normal University, Nanchang 330013, China,Jiangxi Key Laboratory of Surface Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China;

    High Level Engineering Research Center of Biopharmaceutical Molecules and Diagnostic Apparatuses, Jiangxi Provincial Colleges and Universities, Jiangxi Science and Technology Normal University, Nanchang 330013, China,Jiangxi Key Laboratory of Surface Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China;

    Jiangxi Key Laboratory of Surface Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China;

    High Level Engineering Research Center of Biopharmaceutical Molecules and Diagnostic Apparatuses, Jiangxi Provincial Colleges and Universities, Jiangxi Science and Technology Normal University, Nanchang 330013, China,Jiangxi Key Laboratory of Surface Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China;

  • 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);
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  • 正文语种 eng
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