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Metal-free C60/CNTs/g-C3N4 ternary heterostructures: synthesis and enhanced visible-light-driven photocatalytic performance

机译:无金属的C60 / CNT / g-C3N4三元异质结构:合成和增强的可见光驱动的光催化性能

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A metal-free C60/CNTs/g-C3N4 nanoheterostructure with excellent visible-light photocatalysis for rhodamine B (Rh B) degradation has been reported. Via a convenient low-temperature solution-phase method, g-C3N4 nanosheets can serve as substrate for dispersion of C60/CNTs. The loading of C60/CNTs onto g-C3N4 nanosheets surfaces significantly enhanced visible-light-driven photocatalytic activity of g-C3N4 catalyst, for oxidation of organic pollutant (Rh B, 100%). Excellent photocatalytic properties of C60/CNTs/g-C3N4 can be predominantly attributed to the intimate interfacial contact among constructing compounds, increased specific surface area and enhanced light adsorption efficiency resulted from C60/CNTs carbon materials. Particularly, the synergistic heterostructure interaction remarkably hinders the electron–hole pairs recombination, giving rise to significantly enhanced photocatalytic performance of C60/CNTs/g-C3N4 in comparison with other counterparts.
机译:具有出色可见光催化罗丹明B(Rh B)降解性能的无金属C 60 / CNTs / gC 3 N 4 纳米异质结构被报道。通过一种方便的低温固溶相方法,g-C 3 N 4 纳米片可以作为分散C 60 / CNTs的基质。 C 60 / CNT在gC 3 N 4 纳米片表面上的负载显着增强了可见光驱动的gC 3的光催化活性 N 4 催化剂,用于氧化有机污染物(Rh B,100%)。 C 60 / CNTs / gC 3 N 4 的优异光催化性能主要归因于构建化合物之间的紧密界面接触,比表面积增加C 60 / CNTs碳材料产生的面积和提高的光吸收效率。特别是,协同异质结构相互作用显着阻碍了电子-空穴对的重组,从而显着增强了C 60 / CNTs / gC 3 N 4 < / sub>与其他同类产品相比。

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