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Formation of g-C3N4 Nanotubes towards Superior Photocatalysis Performance

机译:形成G-C3N4纳米管朝向优越的光催化性能

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Poor charge separation efficiency seriously limits the application of graphitic carbon nitride (g-C3N4) for water splitting. Herein, g-C3N4 nanotubes were created to enhance charge carrier separation for superior H-2 evolution via a thermal polymerizing reaction using melamine crystals prepared through a transitional metal derived re-crystalline process. Melamine crystals were grown with help of transitional metal ions (Fe3+, Co2+, Ni2+, and Mn2+). As prepared crystals have regular shape with an average size of similar to 20 mu m. The growth of (002) facet was limited and another facets corresponding to (011), (210) and (311) promised. The tubular shape is firstly ascribed to the traces amount of transition metal ions in the crystal promise formation of tubular structure. Another key is that regular crystals with low surface energy slow down polycondensation reaction. The tubular g-C3N4 revealed superior photocatalysis performance. Sample Fe3+ R-650 CN prepared using Fe3+ ions modified crystals exhibited enhanced absorbance at 500 nm and decreased band gap. Tubular morphology accelerated electron transfer along the axial direction. The sample revealed the highest photocatalytic hydrogen evolution rate of 7538 mu mol h(-1) g(-1), which is nearly 13.5 times high compared with g-C3N4 nanosheets prepared using similar conditions without transitional metal ions.
机译:差的电荷分离效率严重限制了石墨碳氮化物(G-C3N4)对水分裂的应用。在此,产生G-C3N4纳米管以通过通过过渡金属衍生的重结晶方法制备的三聚氰胺晶体通过热聚合反应增强用于优异的H-2进化的电荷载体分离。在过渡金属离子(Fe 3 +,CO 2 +,Ni2 +和Mn2 +)的帮助下生长三聚氰胺晶体。由于制备的晶体具有规则形状,平均尺寸与20μm相似。 (002)刻面的生长是有限的,并且对应于(011),(210)和(311)的另一个方面承诺。第一管状形状首先归因于晶体非承诺形成管状结构的过渡金属离子的痕量量。另一个关键是具有低表面能慢缩小缩聚反应的规则晶体。管状G-C3N4显示出优异的光催化性能。使用Fe3 +离子改性晶体制备的样品Fe3 + R-650 CN在500nm处表现出增强的吸光度并降低带隙。管状形态沿轴向加速电子传递。该样品显示出7538μmolH(-1)g(-1)的最高光催化氢进化速率,与使用在没有过渡金属离子的类似条件制备的G-C3N4纳米片相比,与G-C3N4纳米片相比近13.5倍。

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