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Ru/TiO2-P催化剂的制备及其电催化析氢性能

作者:时间:2022-10-19点击数:

Ru/TiO2-P催化剂的制备及其电催化析氢性能


全文下载: 202205005.pdf


文章编号: 1672-6987202205-0036-07 DOI 10.16351/j.1672-6987.2022.05.005


周士正, 秦清* 刘希恩* 唐林生(青岛科技大学 化工学院;生态化工国家重点实验室培育基地,山东 青岛 266042


摘要: 采用一步低温水热法和后续磷化处理制备了Ru/TiO2-P催化剂。利用X-射线衍射(XRD)、透射电子显微镜(TEM)和X-射线光电子能谱(XPS)等手段对催化剂进行了表征。研究了该催化剂在05 mol·L-1 H2SO4溶液中的电催化析氢性能,达到10 mA·cm-2的电流密度时过电势仅为55 mV且经过2 000圈的循环伏安测试后催化活性没有衰减,表明其良好的电催化析氢活性和稳定性。这种优异的性能主要归因于两个方面:(1)磷化过程调控晶粒尺寸,形成更多的粒子间晶界,暴露更多的活性位点;(2)增磷反应后磷以PO3-4形式存在,其氧原子可作为H*吸附位点,增强了催化剂对H*中间体的吸附能力,从而提升催化剂活性。


关键词: 电催化; 析氢; 二氧化钛; 磷化; 三氯化钌


中图分类号: O 614文献标志码: A

引用格式:周士正, 秦清, 刘希恩, . Ru/TiO2-P催化剂的制备及其电催化析氢性能[J. 青岛科技大学学报(自然科学版), 2022, 43(5): 36-42.


ZHOU Shizheng, QIN Qing, LIU Xien, et al. Preparation and hydrogen evolution performance of Ru/TiO2-PJ. Journal of Qingdao University of Science and TechnologyNatural Science Edition), 2022 435): 36-42.


Preparation and Hydrogen Evolution Performance of Ru/TiO2-P


ZHOU Shizheng, QIN Qing, LIU Xien, TANG Linsheng

(College of Chemical Engineering State Key Laboratory Base of Eco-Chemical Engineering,

Qingdao University of Science and Technology, Qingdao 266042, China)


Abstract: Ru/TiO2-P as a highly active HER electrocatalyst was synthesized by one-step hydrothermal method under low temperature combining with subsequently phosphorization treatment. The catalyst was characterized by methods of X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The electrocatalytic hydrogen evolution reaction (HER) performance of Ru/TiO2-P was investigated in 0.5 mol·L-1 H2SO4 electrolyte, which exhibits high activity with a low overpotential of 55 mV at a current density of 10 mA·cm-2 as well as excellent stability. Two possible reasons are contributed to the high performance of Ru/TiO2-P catalyst: First, the size of the nanoparticles was tuned by the phosphorization, coupled with the formation of more inter-particle grain boundaries, which can expose more active sites; Second, there are PO3-4 existed in the catalyst after phosphorization and the oxygen in the PO3-4 groups can be served as the active sites for H* adsorption, which can enhance the capability to the adsorption of H*, and thus, improving the catalytic activity.


Key words: electrocatalysts; hydrogen evolution reaction; titanium dioxide; phosphorization; ruthenium trichloride


收稿日期: 2021-09-02

基金项目: 山东省自然科学基金项目(ZR2018BB008).

作者简介: 周士正(1991—),,博士研究生.*通信联系人.







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