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CdS–MoS2 heterostructures on Mo substrates via in situ sulfurization for efficient photoelectrochemical hydrogen generation

机译:Mo衬底上原位硫化的CdS–MoS 2 异质结构有效产生光电化学氢

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A CdS–MoS2 photoelectrode with a double-layer core–shell structure was prepared using a simple electrodeposition–in situ sulfurization method on a Mo substrate. The photocatalytic activity of as-prepared electrodes was evaluated using a photoelectrochemical H2-generation experiment. The photocurrent and photon–electron conversion efficiency of the CdS–MoS2 photoelectrode were nearly double those of a CdS photoanode prepared on FTO glass. The high activity of the CdS–MoS2 photoelectrode was due to the higher separation efficiency of carriers caused by the formed CdS–MoS2 Janus heterojunction structure, which made directional transmission and electron–hole separation possible. Our experiments show that, in addition to being a good co-catalyst in powder material for photocatalytic hydrogen production, MoS2 can also be used as an electron acceptor layer to enhance electron–hole separation.
机译:采用简单的电沉积-原位硫化法在Mo上制备了具有双层核-壳结构的CdS-MoS 2 光电极基质。使用光电化学H 2 生成实验评估制备电极的光催化活性。 CdS-MoS 2 光电极的光电流和光电子转换效率几乎是在FTO玻璃上制备的CdS光电阳极的两倍。 CdS–MoS 2 光电极的高活性是由于形成的CdS–MoS 2 Janus异质结结构,使得定向传输和电子-空穴分离成为可能。我们的实验表明,MoS 2 除了是粉末状材料中用于光催化制氢的良好助催化剂外,还可以用作电子受体层来增强电子–孔分离。

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