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Ionic liquid/surfactant-hydrothermal synthesis of dendritic PbS@CuS core-shell photocatalysts with improved photocatalytic performance

机译:具有改进的光催化性能的离子液/表面活性剂 - 水土壳光催化剂的树突式PBS - Cus核 - 壳光催化剂

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Dendritic PbS@CuS core-shell photocatalysts were synthesized with a two-step method: a dendritic PbS core was formed with an ionic liquid/surfactant-assisted hydrothermal method; a CuS shell was grown with an ionexchange method. Highly active production of H-2 with these dendritic PbS@CuS photocatalysts is reported for the first time. The surface chemistry, morphology, and properties of the crystal lattice of these core-shell nanomaterials were investigated. The effects of the content of the copper (II) nitrate precursor in the nanomaterials on the charge separation, optical properties, and activity for the production of H-2 were investigated. The interfacial charge-transfer behaviors of the composite nanomaterials were studied with Cu L-3-edge near-edge X-ray-absorption fine-structure (NEXAFS) spectra in situ. A mechanism is proposed based on the results of NEXAFS spectra monitored in situ before and after exposure to solar light. The photoelectron was transferred from CuS to PbS. The proportions of the CuS shells in these dendritic PbS@CuS photocatalysts were optimized to achieve a maximum activity 1736 mu mol h(-1) g(-1) of hydrogen production.
机译:树枝状的PbS @的CuS芯 - 壳光催化剂用两步法合成:树枝状的PbS芯用的离子液体形成/表面活性剂辅助的水热法;一个的CuS壳用一种离子交换方法生长。与这些树枝状的PbS @的CuS的光催化剂活性高的生产H-2报道首次。表面化学性质,形态和这些核 - 壳纳米材料的晶格的性能进行了研究。在电荷分离,光学特性,以及活性用于生产H-2的纳米材料的铜(II)硝酸盐前体的含量的影响。该复合纳米材料的界面的电荷转移行为进行了研究了铜L-3-边缘近边X射线吸收精细结构(NEXAFS)光谱原位。基于NEXAFS光谱的结果,提出了一种机制中就地监测之前和暴露于阳光后。光电子从硫化铜转移到PBS中。在这些树枝状的PbS @的CuS的光催化剂的硫化铜壳的比例进行优化以实现最大活性氢生产的1736亩摩尔H(-1),克(-1)。

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