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Multistage Polymerization Design for g-C3N4 Nanosheets with Enhanced Photocatalytic Activityby Modifying the Polymerization Process of Melamine

机译:具有增强的光催化活性的g-C3N4纳米片的多阶段聚合设计通过改变三聚氰胺的聚合过程

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摘要

Graphene-like g-C3N4 nanosheets (NSs) have been successfully synthesized with a modified polymerization process of melamine by cocondensation with volatile salts. Volatile ammonium salts such as urea–NH4Cl/(NH4)2SO4/(NH4)3PO4 were added with melamine to modulate the thermodynamic process during polymerization and optimize the structure formation in situ. The surface area, surface structure, and surface charge state of the obtained g-C3N4 NSs could be controlled by simply adjusting the mass ratio of the melamine/volatile ammonium salt. As a consequence, the g-C3N4 NSs exhibited much higher activity than bulk g-C3N4 for the photocatalytic degradation of target pollutants (rhodamine B, methylene blue, and methyl orange), and it also exhibited greater hydrogen evolution under visible light irradiation with an optimal melamine/volatile ammonium salt ratio. The as-prepared g-C3N4 NSs with melamine–urea–NH4Cl showed the highest visible light photocatalytic H2 production activity of 1853.8 μmol·h–1·g–1, which is 9.4 times higher than that of bulk g-C3N4 from melamine. The present study reveals that the synergistic effect of the enhanced surface area, surface structure, and surface charge state is the key for the enhancementof photocatalytic degradation and hydrogen evolution, which couldbe controlled by the proposed strategy. The result is a good explanationfor the hypothesis that adding properly selected monomers can trulyregulate the polymerization process of melamine, which is beneficialfor obtaining g-C3N4 NSs without molecular self-assembly.Considering the inexpensive feedstocks used, a simple synthetic controllingmethod provides an opportunity for the rational design and synthesis,making it decidedly appealing for large-scale production of highlyphotocatalytic, visible-sensitizable, metal-free g-C3N4 photocatalysts.
机译:石墨烯样g-C3N4纳米片(NSs)已成功地通过三聚氰胺的改性聚合工艺与挥发性盐共缩合而合成。挥发性铵盐(例如尿素-NH4Cl /(NH4)2SO4 /(NH4)3PO4)与三聚氰胺一起加入,以调节聚合过程中的热力学过程并优化原位结构。可以通过简单地调节三聚氰胺/挥发性铵盐的质量比来控制所获得的g-C 3 N 4 NS的表面积,表面结构和表面电荷状态。结果,对于目标污染物(若丹明B,亚甲基蓝和甲基橙)的光催化降解,g-C3N4 NSs的活性比块状g-C3N4高得多,并且在可见光照射下,H-C3N4 NSs还表现出更大的氢释放。最佳三聚氰胺/挥发性铵盐比率。制备的三聚氰胺-脲-NH 4 Cl的g-C3N 4 NSs可见光催化H 2 的最高生产活性为1853.8 μmol·h –1 ·g –1 ,是批量gC 3 N 4 来自三聚氰胺。本研究表明,增强的表面积,表面结构和表面电荷状态的协同效应是增强的关键。的光催化降解和氢的释放由所提议的策略控制。结果是一个很好的解释假设添加适当选择的单体可以真正调节三聚氰胺的聚合过程,这是有益的获得没有分子自组装的g-C 3 N 4 NSs。考虑到所使用的廉价原料,简单的合成控制该方法为合理设计和综合提供了机会,绝对吸引了大规模生产光催化,可见光敏感,不含金属的g-C 3 N 4 光催化剂。

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