Li Yuhan, Sun Yanjuan, Dong Fan, Ho Wing-Kei
Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, College of Environmental and Biological Engineering, Chongqing Technology and Business University, China; Department of Science and Environmental Studies, The Centre for Education in Environmental Sustainability, The Hong Kong Institute of Education, Hong Kong.
Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, College of Environmental and Biological Engineering, Chongqing Technology and Business University, China.
J Colloid Interface Sci. 2014 Dec 15;436:29-36. doi: 10.1016/j.jcis.2014.09.004. Epub 2014 Sep 16.
Bulk graphitic carbon nitride (CN) suffers from small surface area and high recombination of charge carriers, which result in low photocatalytic activity. To enhance the activity of g-C3N4, the surface area should be enlarged and charge carrier separation should be promoted. In this work, a combined strategy was employed to dramatically enhance the activity of bulk g-C3N4 by simultaneously introducing mesoporous structure and hybridizing with graphene/graphene oxide. The mesoporous g-C3N4/graphene (MCN-G) and mesoporous g-C3N4/graphene oxide (MCN-GO) nanocomposites with enhanced photocatalytic activity (NO removal ratio of 64.9% and 60.7%) were fabricated via a facile sonochemical method. The visible light-harvesting ability of MCN-G and MCN-GO hybrids was enhanced and the conduction band was negatively shifted when 1.0 wt% graphene/graphene oxide was incorporated into the matrix of MCN. As electronic conductive channels, the G/GO sheets could efficiently facilitate the separation of chare carriers. MCN-G and MCN-GO exhibited drastically enhanced visible light photocatalytic activity toward NO removal. The NO removal ratio increased from 16.8% for CN to 64.9% for MCN-G and 60.7% for MCN-GO. This enhanced photocatalytic activity could be attributed to the increased surface area and pore volume, improved visible light utilization, enhanced reduction power of electrons, and promoted separation of charge carriers. This work demonstrates that a combined strategy is extremely effective for the development of active photocatalysts in environmental and energetic applications.
块状石墨相氮化碳(CN)存在比表面积小和电荷载流子复合率高的问题,这导致其光催化活性较低。为了提高g-C3N4的活性,需要增大其表面积并促进电荷载流子的分离。在这项工作中,采用了一种组合策略,通过同时引入介孔结构并与石墨烯/氧化石墨烯杂交,显著提高块状g-C3N4的活性。通过简便的超声化学方法制备了具有增强光催化活性(NO去除率分别为64.9%和60.7%)的介孔g-C3N4/石墨烯(MCN-G)和介孔g-C3N4/氧化石墨烯(MCN-GO)纳米复合材料。当1.0 wt%的石墨烯/氧化石墨烯掺入MCN基体中时,MCN-G和MCN-GO杂化物的可见光捕获能力增强,导带负移。作为电子传导通道,G/GO片层能够有效地促进电荷载流子的分离。MCN-G和MCN-GO对NO去除表现出显著增强的可见光光催化活性。NO去除率从CN的16.8%提高到MCN-G的64.9%和MCN-GO的60.7%。这种增强的光催化活性可归因于表面积和孔体积的增加、可见光利用率的提高、电子还原能力的增强以及电荷载流子分离的促进。这项工作表明,组合策略对于开发用于环境和能源应用的活性光催化剂极其有效。