现代化工2024,Vol.44Issue(7) :156-160,168.DOI:10.16606/j.cnki.issn0253-4320.2024.07.028

碱水热法制备Ti3C2-Ag3PO4光催化剂及其光催化性能研究

Preparation of Ti3C2-Ag3PO4 photocatalyst via alkali hydrothermal method and evaluation of its photocatalytic performance

徐竞帆 周绿山 沈琪 熊信洁 刘丹 李颖 张玉 唐佳文
现代化工2024,Vol.44Issue(7) :156-160,168.DOI:10.16606/j.cnki.issn0253-4320.2024.07.028

碱水热法制备Ti3C2-Ag3PO4光催化剂及其光催化性能研究

Preparation of Ti3C2-Ag3PO4 photocatalyst via alkali hydrothermal method and evaluation of its photocatalytic performance

徐竞帆 1周绿山 1沈琪 1熊信洁 1刘丹 1李颖 1张玉 1唐佳文1
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作者信息

  • 1. 四川文理学院化学化工学院,四川 达州 635000
  • 折叠

摘要

通过碱水热反应合成了Ti3C2,并以其为载体制备了不同负载量的Ti3C2-Ag3PO4 光催化剂.利用FT-IR、XRD、SEM、XPS等对光催化剂进行表征.结果表明,在 240℃水热条件下,碱刻蚀法制备的Ti3C2 为刻蚀程度较低的片层结构,同时材料中有微量的TiO2 存在,同时Ag3PO4 以立方相的形式负载到Ti3C2 载体表面.随着Ag3PO4 负载量的增加,Ti3C2-Ag3PO4的光催化活性逐渐增大,在催化剂质量为0.01 g、反应时间为 60 min时,Ti3C2-Ag3PO4-85%对亚甲基蓝的降解率达到 95%.Ti3C2 与Ag3PO4 异质结的存在使其具有较强的电荷分离能力和优异的光催化性能.

Abstract

Ti3C2 is synthesized through alkaline hydrothermal reaction,and used as support to prepare Ti3C2-Ag3PO4 photocatalysts with different loading amount.The photocatalysts are characterized by means of FT-IR,XRD,SEM and XPS.It is indicated that Ti3C2 prepared through alkali etching method at 240℃ hydrothermal condition presents a layer structure with low etching degree.In addition,there are trace TiO2 in Ti3C2 material,and Ag3PO4 has been supported on the surface of Ti3C2 support.The photocatalytic activity of Ti3C2-Ag3PO4 increases with the higher Ag3PO4 loading amount.The degradation rate of methylene blue by Ti3C2-Ag3PO4-85%can reach 95%when the usage of the catalyst is 0.01 g and the reaction performs 60 min.The presence of heterojunction between Ti3C2 and Ag3PO4 makes the catalyst have strong charge separation ability and excellent photocatalytic performance.

关键词

碱水热法/Ti3C2-Ag3PO4/光催化

Key words

alkaline hydrothermal method/Ti3C2-Ag3PO4/photocatalysis

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基金项目

四川省科技厅项目(2022YFG0277)

绿色催化四川省高校重点实验室项目(LZJ2202)

四川省大学生创新创业训练项目(S202310644044)

出版年

2024
现代化工
中国化工信息中心

现代化工

CSTPCDCSCD北大核心
影响因子:0.553
ISSN:0253-4320
参考文献量23
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