摘要
采用一步低温水热法和后续磷化处理制备了Ru/TiO_(2)-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)H_(2)SO_(4)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PO_(4)^(3-)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。
Ru/TiO_(2)-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/TiO_(2)-P was investigated in 0.5 mol·L^(-1)H_(2)SO_(4)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/TiO_(2)-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 PO_(4)^(3-)existed in the catalyst after phosphorization and the oxygen in the PO_(4)^(3-)groups can be served as the active sites for Hadsorption, which can enhance the capability to the adsorption of H, and thus, improving the catalytic activity.
作者
周士正
秦清
刘希恩
唐林生
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)
出处
《青岛科技大学学报(自然科学版)》
CAS
2022年第5期36-42,共7页
Journal of Qingdao University of Science and Technology:Natural Science Edition
基金
山东省自然科学基金项目(ZR2018BB008)。
关键词
电催化
析氢
二氧化钛
磷化
三氯化钌
electrocatalysts
hydrogen evolution reaction
titanium dioxide
phosphorization
ruthenium trichloride