无机材料学报 ›› 2023, Vol. 38 ›› Issue (5): 503-510.DOI: 10.15541/jim20220413

所属专题: 【能源环境】光催化(202310)

• 研究论文 • 上一篇    下一篇

TiHAP@g-C3N4异质结的制备及光催化降解甲基橙

伍林(), 胡明蕾, 王丽萍(), 黄少萌, 周湘远   

  1. 中国矿业大学 环境与测绘学院, 徐州 221116
  • 收稿日期:2022-07-15 修回日期:2022-11-11 出版日期:2022-11-16 网络出版日期:2022-11-16
  • 通讯作者: 王丽萍, 教授. E-mail: wlpcumt@126.com
  • 作者简介:伍 林(1999-), 男, 硕士研究生. E-mail: TS21160095A31LD@cumt.edu.cn
  • 基金资助:
    国家自然科学基金(51974314)

Preparation of TiHAP@g-C3N4 Heterojunction and Photocatalytic Degradation of Methyl Orange

WU Lin(), HU Minglei, WANG Liping(), HUANG Shaomeng, ZHOU Xiangyuan   

  1. School of Environment and Spatial Informatics, China University of Mining and Technology, Xuzhou 221116, China
  • Received:2022-07-15 Revised:2022-11-11 Published:2022-11-16 Online:2022-11-16
  • Contact: WANG Lingping, professor. E-mail: wlpcumt@126.com
  • About author:WU Lin (1999-), male, Master candidate. E-mail: TS21160095A31LD@cumt.edu.cn
  • Supported by:
    National Natural Science Foundation of China(51974314)

摘要:

通过水热法合成了钛羟基磷灰石(TiHAP)与g-C3N4复合光催化剂(TiHAP@g-C3N4), 并对其结构和光学特性进行表征, 通过甲基橙(MO)降解实验评价其光催化活性。结果表明:样品中短棒状TiHAP生长在g-C3N4表面, 均保持原有晶型和化学结构; 制备的TiHAP@g-C3N4纯度高, 比表面积达107.92 m2/g, 较TiHAP、g-C3N4分别增大约135%、44%; 在TiHAP@g-C3N4添加量为1.0 g/L、pH 7条件下, 120 min内MO降解率达96.35%; 3次循环实验降解率保持在80.02%以上, TiHAP@g-C3N4光催化性能良好且结构稳定。空穴(h+)在MO降解过程中作用最大, ·O2-与·OH的作用递减。TiHAP@g-C3N4异质结的构建, 增强了对光的吸收, 提高了光生电子-h+的分离效率, 保留了氧化还原性更强的TiHAP价带h+和g-C3N4导带电子, 从而提升了光催化性能。

关键词: 紫外光催化, TiHAP@g-C3N4, 甲基橙, 异质结, 光生电子-空穴

Abstract:

A composite photocatalyst (TiHAP@g-C3N4) consisting of Ti doped hydroxyapatite and g-C3N4 was synthesized through hydrothermal route. Its structure and optical property were characterized by various means and photocatalytic activity was evaluated through methyl orange (MO) degradation experiments. Results show that short rod-shaped TiHAP in the sample grows on the surface of g-C3N4. Both TiHAP and g-C3N4 maintain their original crystal shape and chemical structure. As-prepared TiHAP@g-C3N4 is of high purity with specific surface area of 107.92 m2/g, which is increased about 135% and 44% as compared with sole TiHAP and sole g-C3N4, respectively. The highest MO degradation rate of 96.35% is achieved within 120 min by TiHAP@g-C3N4 at the concentration of 1.0 g/L and pH 7. More than 80.02% of MO was removed in every of three cyclic tests, demonstrating good and stable photocatalytic performance of TiHAP@g-C3N4. Holes (h+) play the largest role in the MO degradation process, followed by ·O2- and ·OH. The constructed TiHAP@g-C3N4 heterojunction enhances light absorption, improves separation efficiency of photoelectrons-h+, and preserves more redox-prone TiHAP valence band h+ and g-C3N4 conduction band electrons. Therefore, as-synthesized TiHAP@g-C3N4 can be a promising catalyst in photocatalytic degradation.

Key words: ultraviolet photocatalysis, TiHAP@g-C3N4, methyl orange, heterojunction, photoelectron-hole

中图分类号: