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凹凸棒石/g-C3N4复合材料的制备及其电催化析氧性能研究
引用本文:张盛,蒋亿,纪媛媛,杜莹,盛振环,殷竟洲,李乔琦,张莉莉.凹凸棒石/g-C3N4复合材料的制备及其电催化析氧性能研究[J].无机材料学报,2019,34(8):803-810.
作者姓名:张盛  蒋亿  纪媛媛  杜莹  盛振环  殷竟洲  李乔琦  张莉莉
作者单位:淮阴师范学院 化学化工学院, 江苏省低维材料化学重点实验室, 江苏省环境工程实验室, 淮安 223300
基金项目:国家自然科学基金(51472101);江苏省六大人才高峰(JY-31);江苏省自然科学基金(BK20161305);江苏省高校大学生创新计划(201710323004Z)
摘    要:以凹凸棒石(ATP)为载体, 通过原位沉积, 结合冷冻干燥、程序焙烧工艺在其表面负载不同质量分数的类石墨相氮化碳(g-C3N4)薄层材料, 制备系列ATP/g-C3N4复合材料用于电催化析氧反应, 产物标识为ATP/g-C3N4-w (质量分数w = mATP: (mATP + mg-C3N4)=0.33、0.40、0.50、0.67), 并研究在0.1 mol/L KOH的电解液中的电催化析氧性能。结果表明: g-C3N4薄层通过Si-O-C键牢固负载于凹凸棒石表面, 从而有效调变g-C3N4表面的电子层结构, 提供更多的催化活性位点。电催化析氧测试的结果表明: ATP/g-C3N4-0.50具有最优的析氧催化性能, 在10 mA/cm 2电流密度下其析氧过电位为410 mV, 塔菲尔斜率为118 mV/dec, 并表现出优异的析氧稳定性。

关 键 词:凹凸棒石  石墨相氮化碳  电催化  析氧反应  
收稿时间:2018-08-15
修稿时间:2018-10-09

Attapulgite/g-C3N4 Composites: Synthesis and Electrocatalytic Oxygen Evolution Property
ZHANG Sheng,JIANG Yi,JI Yuan-Yuan,DU Ying,SHENG Zhen-Huan,YIN Jing-Zhou,LI Qiao-Qi,ZHANG Li-Li.Attapulgite/g-C3N4 Composites: Synthesis and Electrocatalytic Oxygen Evolution Property[J].Journal of Inorganic Materials,2019,34(8):803-810.
Authors:ZHANG Sheng  JIANG Yi  JI Yuan-Yuan  DU Ying  SHENG Zhen-Huan  YIN Jing-Zhou  LI Qiao-Qi  ZHANG Li-Li
Affiliation:Jiangsu Environmental Engineering Laboratory, Jiangsu Key Laboratory for Low-dimension Materials, School of Chemistry and Chemical Enginering, Huaiyin Normal University, Huaian 223300, China
Abstract:A novel kind of electrocatalytic oxygen evolution catalyst was fabricated by introducing g-C3N4 ultrathin films onto the surface of attapulgite (ATP) via a simple in-situ depositing technique, combined with freeze-drying and programmed roasting process. The obtained product was identified as ATP/g-C3N4. In order to achieve the best catalyst, a series of ATP/g-C3N4 composites with different mass fraction of ATP were obtained and marked as ATP/g-C3N4-w, where w represents the mass fraction of ATP (w =mATP: (mATP + mg-C3N4)= 0.33, 0.40, 0.50, 0.67). Results show that g-C3N4 thin layers are uniformly loaded onto the ATP surface via the chemical bond (Si-O-C), which is beneficial to tailor the surface electronic structure of g-C3N4 and provide more active sites. Their electrocatalytic oxygen evolution properties in 0.1 mol/L KOH were investigated. It is found that ATP/g-C3N4-0.50 presents the best oxygen evolution catalytic performance and has excellent oxygen evolution stability. Its oxygen evolution over potential is 410 mV and the Tafel slope is 118 mV/dec at a current density of 10 mA/cm 2. The results suggest that ATP/ g-C3N4-0.50 can be used as a potential oxygen evolution catalyst.
Keywords:attapulgite  g-C3N4  electrocatalysis  oxygen evolution veaction  
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