Jin Zhiliang, Yan Xian, Hao Xuqiang
School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan 750021, PR China; Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan 750021, PR China; Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.
School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan 750021, PR China; Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan 750021, PR China; Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.
J Colloid Interface Sci. 2020 Jun 1;569:34-49. doi: 10.1016/j.jcis.2020.02.052. Epub 2020 Feb 15.
Enriching the active sites of catalysts and artificially regulating the directional migration of photogenerated carriers are effective means to improve the catalytic activity of photocatalysts. In this work, polyvinylpyrrolidone (PVP) is used as the morphological modifier to prepare MoS with three-dimensional (3D) nanoflower structure. Compared with two-dimensional (2D) MoS nanosheets, three-dimensional nanoflower structure weakens the van der Waals force between nanosheets and inhibits the stacking between layers, thus exposing the high-density active sites of MoS nanoflower. The CoWO nanoparticles are successfully anchored to MoS by in-situ growth, forming the MoS/CoWO p-n heterojunction photocatalyst. The high photosensitivity of MoS increases the utilization of MoS/CoWO p-n heterojunction to visible light. The unique 3D nanoflower structure of MoS results in that CoWO nanoparticles are dispersed well on the surface of MoS, which prevents CoWO agglomeration. Based on the high efficiency of charge separation, abundant active sites and excellent property of visible light response, the hydrogen evolution rate of MoS/CoWO-40 reached 9414.4 μmol g h.
丰富催化剂的活性位点并人工调控光生载流子的定向迁移是提高光催化剂催化活性的有效手段。在这项工作中,聚乙烯吡咯烷酮(PVP)用作形貌改性剂来制备具有三维(3D)纳米花结构的MoS。与二维(2D)MoS纳米片相比,三维纳米花结构减弱了纳米片之间的范德华力并抑制了层间堆叠,从而暴露出MoS纳米花的高密度活性位点。通过原位生长将CoWO纳米颗粒成功锚定在MoS上,形成MoS/CoWO p-n异质结光催化剂。MoS的高光敏性提高了MoS/CoWO p-n异质结对可见光的利用率。MoS独特的3D纳米花结构使得CoWO纳米颗粒很好地分散在MoS表面,从而防止了CoWO的团聚。基于高效的电荷分离、丰富的活性位点和优异的可见光响应性能,MoS/CoWO-40的析氢速率达到了9414.4 μmol g h。