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In situ self-assembly of 3D hierarchical 2D/2D CdS/g-C3N4 hereojunction with excellent photocatalytic performance

机译:在这里的3D层次2D / 2D CDS / G-C3N4的原位自组装在此具有出色的光催化性能

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摘要

A novel hierarchical 2D/2D CdS/g-C3N4 hybridarchitecture was synthesized via a hydrothermal method and then characterized by XRD, FTIR, SEM, EDS, UV-vis DRS, PL, BET, and EIS. The results showed the combination of CdS and g-C3N4 changed the growth orientation of dendritic CdS nanocrystallines and promoted the high degree of exfoliation of g-C3N4, which provided the close nanosheet/nanosheet 2D/2D contact interface and large specific surface area, resulting in the effective separation of the photo-generated carrier pairs. The photocatalytic activity of CdS/g-C3N4 was 6.93 and 3.64 times higher than that of the pure g-C3N4 and CdS samples, respectively, in the degradation of RhB under visible light irradiation. The CdS/g-C3N4 showed no obvious loss of the photocatalytic activity and little change of structure after three repeated runs, which is vital in the application of photocatalyst. This could be contributed to the reinforced hierarchical 3D architecture constructed through the dendritic CdS nanosheet penetrating into g-C3N4 interlayers. The possible mechanism for formation and photocatatlytic activity of the CdS/g-C3N4 architecture was proposed.
机译:通过水热法合成了一种新的等级2D / 2D CDS / G-C3N4杂交建筑,然后通过XRD,FTIR,SEM,EDS,UV-VIS DRS,PL,BET和EIS表征。结果表明,Cd和G-C3N4的组合改变了树突式Cds纳米晶体的生长取向,并促进了G-C3N4的高剥离,提供了紧密纳米片/纳米片2D / 2D接触界面和大的比表面积,得到在有效分离照片产生的载体对。 Cds / G-C3N4的光催化活性分别比纯G-C3N4和CDS样品高出6.93和3.64倍,在可见光照射下RHB的降解中。 CDS / G-C3N4显示出明显的光催化活性损失,三次重复运行后的结构几乎没有变化,这对于光催化剂的应用至关重要。这可以有助于通过渗透到G-C3N4中间层的树突CDS纳米片构成的增强层次3D架构。提出了CDS / G-C3N4架构的形成和光涂覆的可能机制。

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