无机材料学报 ›› 2019, Vol. 34 ›› Issue (11): 1200-1204.DOI: 10.15541/jim20190009 CSTR: 32189.14.10.15541/jim20190009

• 研究快报 • 上一篇    下一篇

铂修饰二氧化钛纳米片的制备及其光电催化析氢反应研究

苏琨1,2,3,张亚茹3,陆飞3,张君1(),王熙3()   

  1. 1. 内蒙古大学 化学化工学院, 呼和浩特010021
    2. 包头医学院 药学院, 包头 014040
    3. 北京交通大学 理学院,北京100044
  • 收稿日期:2019-01-04 出版日期:2019-11-20 网络出版日期:2019-05-13

Platinum Decorated Titanium Dioxide Nanosheets for Efficient Photoelectrocatalytic Hydrogeu Evolution Reaction

SU Kun1,2,3,ZHANG Ya-Ru3,LU Fei3,ZHANG Jun1(),WANG Xi3()   

  1. 1. School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China
    2. School of Pharmacy, Baotou Medical College, Baotou 014040, China
    3. School of Science, Beijing Jiaotong University, Beijing 100044, China
  • Received:2019-01-04 Published:2019-11-20 Online:2019-05-13
  • Supported by:
    National Natural Science Foundation of China(21665019);National Natural Science Foundation of China(21165011);Natural Science Foundation of the Inner Mongolia Autonomous Region(2015MS0215);The Fundamental Research Funds for the Central Universities(2018JBZ107);The Fundamental Research Funds for the Central Universities(2018RC022);The Fundamental Research Funds for the Central Universities(2017JBM068);The Fundamental Research Funds for the Central Universities(S18I00010);The Fundamental Research Funds for the Central Universities(S17I00010);The Fundamental Research Funds for the Central Universities(S16C00010);The “1000 Youth Talents plan” Project;The “Excellent One Hundred” Project of Beijing Jiaotong University

摘要:

利用静电吸附作用在二氧化钛纳米片上负载铂原子制备了两种不同形态的铂催化剂。SEM、XRD、TEM测试结果表明, 改变铂负载量可以调控铂的形貌结构。在低Pt负载(0.2wt%)下, 铂原子主要是半径约2 nm的纳米簇, 当Pt负载量增加到1wt%时, 铂原子在二氧化钛纳米片上堆积成纳米颗粒。调控Pt负载量和纳米结构, 可以显著提高二氧化钛纳米片催化析氢反应的活性。在AM1.5太阳光照射下, 两种催化剂的塔菲尔斜率都小于100 mV/dec, 分别为56和90 mV/dec。与TiO2-Pt1%催化剂相比, TiO2-Pt0.2%具有更理想的金属-半导体界面, 有利于光生电子迁移至铂纳米簇表面, 因而具有更高的催化活性。本实验为研究更加高效的铂催化剂和其他光电催化剂提供了新的途径。

关键词: 析氢反应, 铂纳米簇, 二氧化钛, 光电催化

Abstract:

Two kinds of platinum catalysts with different morphologies were prepared by loading platinum atoms on titanium dioxide nanosheets via electrostatic adsorption. Scanning electron microscope (SEM), X-ray powder diffraction (XRD) and transmission electron microscope (TEM) characterization show that the morphology and structure of platinum could be controlled by changing the platinum loading. With low Pt loading (0.2wt%), the platinum atoms were mainly nanoclusters with a radius of about 2 nm. When the Pt loading increased to 1wt%, the platinum atoms stack into nanoparticles on the titanium dioxide nanosheets. The catalytic hydrogen evolution activity of titanium dioxide nanosheets can be improved obviously by regulating the platinum loading and nanostructure. Under AM1.5 solar light, the Tafel slope of both catalysts were less than 100 mV/dec, i.e. 56 and 90 mV/dec, respectively. Compared with TiO2-Pt1% catalyst, TiO2-Pt0.2% has a more ideal metal-semiconductor interface, which is favorable for photogenic electrons to migrate to the surface of platinum nanoclusters, and thus perform a higher catalytic activity. This experiment provides a new way for preparing platinum catalysts with high efficiency.

Key words: hydrogen evolution reaction (HER), platinum clusters, titanium dioxide, photoelectrocatalysis

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