首页> 外文期刊>Superlattices and microstructures >Ammonia-evaporation-induced construction of three- dimensional NiO/g-C_3N_4 composite with enhanced adsorption and visible light-driven photocatalytic performance
【24h】

Ammonia-evaporation-induced construction of three- dimensional NiO/g-C_3N_4 composite with enhanced adsorption and visible light-driven photocatalytic performance

机译:氨蒸发诱导的三维NiO / g-C_3N_4复合材料的吸附和可见光驱动的光催化性能增强

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Novel visible light-driven heterostructured NiO/g-C3N4 photocatalyst has been designed and successfully prepared via ammonia-evaporation-induced method. The synthetic strategy consists of grafting the surface of g-C3N4 with Ni(NH3)(6)(2+) complex followed by its hydrolysis at lower pH to form nano-wrinkled thin film of alpha-Ni(OH)(2). The final NiO/g-C3N4 hybrid was obtained after calcination of the Ni(OH)(2)/g-C3N4 precursor at 350 degrees C. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, FTIR, N-2 adsorption/desorption, UV-vis diffuse reflectance and photoluminescence spectroscopy were used to characterize the resulting material. Our results revealed the formation of meso-/macroporous three-dimensional hierarchical honeycomb-like structure with high BET surface area (141 m(2) g(-1)). The photocatalytic performance of the composite under visible light (lambda 400 nm) irradiation was evaluated through degradation of Malachite Green (MG) from aqueous medium at room temperature (25 degrees C). For the sake of comparison, the physico-chemical and photocatalytic properties of the pristine g-C3N4 and nanostructured NiO were also examined. Results indicated that NiO/g-C3N4 is much more active than pristine g-C3N4 and NiO in the photodegradation of MG. The enhanced photocatalytic performance of the composite was mainly attributed to the combination of high adsorption capacity which facilitates the direct redox reactions of dye and the efficient inhibition of photo-generated electron-hole pair recombination. Superoxide radicals (center dot O-2) and photo-generated holes (h(+)) were found to be the main active species in the process. (C) 2018 Elsevier Ltd. All rights reserved.
机译:通过氨蒸发诱导法设计并成功制备了新型可见光驱动的异质结构NiO / g-C3N4光催化剂。合成策略包括用Ni(NH3)(6)(2+)络合物接枝g-C3N4的表面,然后在较低的pH下将其水解以形成纳米皱纹的α-Ni(OH)(2)薄膜。 Ni(OH)(2)/ g-C3N4前体在350摄氏度下煅烧后,获得最终的NiO / g-C3N4杂化物。扫描电子显微镜,透射电子显微镜,X射线衍射,FTIR,N-2吸附/解吸,紫外可见漫反射和光致发光光谱法表征所得材料。我们的结果显示具有高BET表面积(141 m(2)g(-1))的介孔/大孔三维分层蜂窝状结构的形成。通过在室温(25摄氏度)下从水介质中降解孔雀石绿(MG)来评估复合材料在可见光(λ> 400 nm)照射下的光催化性能。为了比较,还检查了原始g-C3N4和纳米结构的NiO的物理化学和光催化性能。结果表明,NiO / g-C3N4比原始g-C3N4和NiO在MG的光降解中更具活性。复合材料增强的光催化性能主要归因于高吸附能力(促进染料的直接氧化还原反应)和有效抑制光生电子-空穴对重组的组合。超氧化物自由基(中心点O-2)和光生空穴(h(+))被发现是该过程中的主要活性物质。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号