标题: 重庆大学化学化工学院杨韬 [打印本页] 作者: guanshengyuan 时间: 2018-5-28 17:13 标题: 重庆大学化学化工学院杨韬 杨韬，教授，博士生导师，1999-2003年在北京大学化学与分子工程学院学习获得学士学位，2008年获得无机化学博士学位。2008年至2011年先后在美国Rutgers University和英国University of Liverpool进行博士后研究。2011加入重庆大学化学化工学院。
联系方式
E-mail: taoyang@cqu.edu.cn.
研究方向
研究领域为无机固体化学，是基于多样化的合成手段制备带有特定功能的材料，综合利用各种结构表征方法研究晶体结构，揭示结构与性质关系，随后进行性能优化和指导新材料的设计合成。
代表性论文、专著和专利
(1) Bi2Ga4O9: An un-doped single-phase photocatalyst for overall water splitting under visible light, J. Catal. 2017, 345, 236-244.
(2) Octahedral-based redox molecular sieve M-PKU-1: isomorphous metal-substitution, catalytic oxidation of sec-alcohol and related catalytic mechanism, J. Catal. 2017, 352, 130-141.
(3) Chemical substitution induced and competitive formation of 6H- and 3C-perovskite structures in Ba3-xSrxZnSb2O9: the coexistence of two perovskites in 0.3 ≤ x ≤ 1.0, Inorg. Chem. 2017, 56, 14335-14344.
(4) β-RE1-xBixB3O6 (RE= Sm, Eu, Gd, Tb, Dy, Ho, Er, Y): Bi3+-substitution induced formation of meta-stable rare earth borates at ambient pressure, Inorg. Chem. 2016, 55, 9276-9283.
(5) Y1-xScxBaZn3GaO7 (0 ≤ x ≤ 1): Structure evolution by Sc-doping and the first example of photocatalytic water reduction in “114” oxides, Inorg. Chem. 2016, 55, 1527-1534.
(6) Ga4B2O9: An Efficient Borate Photocatalyst for Overall Water Splitting without Co-catalyst, Inorg. Chem. 2015, 54, 2945-2949.
(7) ZnGa2-xInxS4 (0 ≤ x ≤ 0.4) and Zn1-2y(CuGa)yGa1.7In0.3S4 (0.1 ≤ y ≤ 0.2): Optimize visible light photocatalytic H2 evolution by fine modulation of band structures,Inorg. Chem. 2015, 54, 2467-2473.
(8) Open-framework Gallium Borate with Boric and Metaboric Acid Molecules inside Structural Channels Showing Photocatalysis to Water Splitting, Inorg. Chem. 2014, 53, 2364-2366.
(9) Systematic Study of Cr3+ Substitution into Octahedra-based Microporous Aluminoborates, Inorg. Chem. 2014, 53, 5600-5608.
(10) Observation of the Sixth Polymorph of BiB3O6: In Situ High-Pressure Raman Spectroscopy and Synchrotron X ray Diffraction Studies on the β Polymorph, Inorg. Chem. 2013, 52, 7460-7466.