Sun Qing, Zhao Yingjie, Qin Feng, Zhang Jian, Wang Bin, Ye Huijian, Sheng Jiawei
College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China.
Wenzhou Institute of Science and Technology, Zhejiang University of Technology, Wenzhou 325011, People's Republic of China.
Nanotechnology. 2021 Mar 26;32(13):135602. doi: 10.1088/1361-6528/abd126.
The BiVO/HNTs hybrid photocatalysts were synthesized by liquid phase precipitation using natural halloysite nanotubes (HNTs) as supporter and Bi(NO)·5HO as resource of Bi. XRD, scanning electron microscopy (SEM), transmission electron microscopy, HRTEM, x-ray photo electron spectroscopy and UV-Vis DRS were used to characterize the samples prepared at different calcination temperatures, and the effects of crystallization, Brunauer-Emmett-Teller specific surface area and morphological structure on the photoactivity were investigated. Results reveal that increasing calcination temperature can accelerate the transition of BiVO from tetragonal to monoclinic and also decrease the surface area of BiVO/HNTs. The SEM results showed that BiVO was successfully coated on HNTs surface with ellipsoid or near rod like morphology, and the obtained BiVO/HNTs had regular nanotube morphology. HRTEM results showed that, the regular fringe spacing of the lattice planes are about 0.474 and 0.364 nm, which is consistent with the (110) and (200) plane of the monoclinic and tetragonal BiVO, confirming the exiting of mixed crystal structure in BiVO/HNTs. BiVO with tetragonal phase (80.02%) and monoclinic phase (19.98%) mixed crystal is loaded on the surface of HNTs with calcinations at 400 °C for 2 h. The structure and Si (Al)-O bond of HNTs can be obviously changed over the calcination temperature of 400 °C. The effect of calcination temperature on photocatalytic reactivity of samples was investigated by degradation of dyes (MB, MO and RhB) under simulated solar light. And the sample calcined at 400 °C with the better mixed crystalline structure and larger specific surface area exhibits significant activity with the removal rate of MB and RhB up to 100% within 4 h. The degradation of MB follows the first order kinetic model. BiVO/HNTs photocatalysts with the band gap of 2.34 eV has higher photocatalytic reaction rate and better sedimentation performance than Degussa P25. The photocatalytic degradation efficiency of BiVO/HNTs for MB was no significant reduction after four times recycles.
采用液相沉淀法,以天然埃洛石纳米管(HNTs)为载体、Bi(NO)₃·5H₂O为铋源,合成了BiVO₄/HNTs复合光催化剂。利用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜、高分辨透射电子显微镜(HRTEM)、X射线光电子能谱和紫外可见漫反射光谱(UV-Vis DRS)对不同煅烧温度下制备的样品进行了表征,并研究了结晶、比表面积和形态结构对光活性的影响。结果表明,提高煅烧温度可加速BiVO₄从四方相转变为单斜相,同时降低BiVO₄/HNTs的比表面积。SEM结果表明,BiVO₄成功地包覆在HNTs表面,呈椭球形或近棒状形态,所得BiVO₄/HNTs具有规则的纳米管形态。HRTEM结果表明,晶格平面的规则条纹间距约为0.474和0.364 nm,与单斜相和四方相BiVO₄的(110)和(200)平面一致,证实了BiVO₄/HNTs中存在混合晶体结构。在400℃煅烧2 h后,具有四方相(80.02%)和单斜相(19.98%)混合晶体的BiVO₄负载在HNTs表面。在400℃以上的煅烧温度下,HNTs的结构和Si(Al)-O键会发生明显变化。通过在模拟太阳光下降解染料(亚甲基蓝(MB)、甲基橙(MO)和罗丹明B(RhB))研究了煅烧温度对样品光催化活性的影响。在400℃煅烧的样品具有较好的混合晶体结构和较大的比表面积,在4 h内对MB和RhB的去除率高达100%,表现出显著的活性。MB的降解遵循一级动力学模型。带隙为2.34 eV的BiVO₄/HNTs光催化剂比德固赛P25具有更高的光催化反应速率和更好的沉降性能。BiVO₄/HNTs对MB的光催化降解效率在四次循环后没有明显降低。