
Citation: Xibao Li, Jie Xiong, Ying Xu, Zhijun Feng, Juntong Huang. Defect-assisted surface modification enhances the visible light photocatalytic performance of g-C3N4@C-TiO2 direct Z-scheme heterojunctions[J]. Chinese Journal of Catalysis, 2019, 40(3): 424-433. doi: 10.1016/S1872-2067(18)63183-3

缺陷辅助表面修饰提高g-C3N4@C-TiO2直接Z型异质结的可见光光催化性能
本课题组曾通过简单的水辅助煅烧法成功制备了纳米多孔g-C3N4,结果发现,多孔g-C3N4光催化活性较体相的明显提高,但光催化效率仍不够理想,原因是光生电子空穴复合较严重.传统的制备C-TiO2的方法亦存在一些不足,如需要添加碳源或碳组分聚集体.我们采用原位掺杂的方法合成了含有一定氧空位和活性位的纳米碳改性的C-TiO2,后辅以简单的化学气相沉积法构建了g-C3N4表面修饰的g-C3N4@C-TiO2.结果表明,相比纯g-C3N4,TiO2及C-TiO2,g-C3N4@C-TiO2具有更高的光催化活性;但其原因及碳掺杂态的影响尚不清楚.基于此,本文采用X射线光电子能谱技术(XPS)、透射电子显微镜(TEM)、电化学阻抗谱(EIS)、光致发光谱(PL)、电子顺磁共振技术(EPR)及理论计算等手段研究了g-C3N4@C-TiO2光催化活性提高的原因和机理.
XPS结果表明,随着碳含量的增加,间隙掺杂产生的O-C键的峰值强度先增大后趋于稳定,而晶格取代掺杂产生的Ti-C键的峰值强度逐渐增大.Ti-O峰的减少进一步证明了更多的碳取代了氧晶格的位置.随着碳掺杂量的增加,C-TiO2的带隙逐渐减小,因而吸收边红移;同时,g-C3N4@C-TiO2的光催化降解效率先升高后降低.g-C3N4@C-TiO2对RhB(苯酚)光降解的最大表观速率常数为0.036(0.039)min-1,分别是纯TiO2,10C-TiO2,g-C3N4和g-C3N4@TiO2的150(139),6.4(6.8),2.3(3)和1.7(2.1)倍.g-C3N4通过π-共轭和氢键与C-TiO2表面紧密结合,在催化剂中引入了新的非局域杂质能级和表面态,可以更有效地分离和转移光生电子,因而光催化活性增加.由此可见,碳掺杂状态和g-C3N4原位沉积表面改性对g-C3N4@C-TiO2复合光催化剂性能的影响很大.
English
Defect-assisted surface modification enhances the visible light photocatalytic performance of g-C3N4@C-TiO2 direct Z-scheme heterojunctions
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Key words:
- Photocatalyst
- / Heterojunction
- / Direct Z-scheme
- / Doping
- / Modification
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