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Metal-free dual-phase full organic carbon nanotubes/g-C3N4 heteroarchitectures for photocatalytic hydrogen production

机译:无金属双相全有机碳纳米管/ G-C3N4用于光催化氢气生产的异质建筑

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摘要

Hydrogen generation from water using solar energy has grown into a promising approach for sustainable energy production. Over the last years, graphitic carbon nitrides (g-C3N4, CN), polymers based on the heptazine-group, have been widely applied as photocatalysts for H-2 evolution. The poor charge separation efficiency of CN is considered the major drawback. Here, we investigated the effect of coupling CN with different types of carbon nanotubes on the charge transfer properties and the photocatalytic H-2 evolution. We used carbon nanotubes (CNTs) of different wall number (single (SWCNTs), double (DWCNTs) and multi-walled (MWCNTs) CNTs) for the development of full-organic CN based composite photocatalysts. Photoactivity was drastically affected by the content but more importantly by the nature of the CNTs. The SWCNTs functionalized CN composites were the most active presenting approximately 2-5 times higher H-2 evolution than the corresponding DWCNTs and MWCNTs functionalized CN under both solar and pure visible light irradiation. Photoactivity was primarily controlled by the improved electronic properties linked with the abundance and stability of photogenerated charges as evidenced by electron paramagnetic resonance spectroscopy. Transient absorption spectroscopy verified the transfer of reactive electrons from CN to CNTs. CNTs functioned as electron acceptors improving charge separation. The data suggest that charge transfer is inversely proportional to the wall number of the CNTs and that photoactivity is directly controlled by the size at the nanoscale of the CNTs used. In the CNTs/CN nanocomposites, photogenerated electrons are transferred more efficiently from CN when SWCNTs are used, providing more available electrons for H-2 production.
机译:使用太阳能的水从水产生的氢气已经发展成为可持续能源生产的有希望的方法。在过去的几年中,基于七肽基团的石墨碳氮化物(G-C3N4,CN),聚合物被广泛应用于H-2进化的光催化剂。 CN的差的电荷分离效率被认为是主要的缺点。在这里,我们研究了在电荷转移性和光催化H-2进化上对不同类型的碳纳米管偶联CN的效果。我们使用不同壁数(单(SWCNT),双(DWCNT)和多壁(MWCNT)CNTs的碳纳米管(CNT)用于开发全有机CN基复合光催化剂。含量的含量大幅度影响,但更重要的是由CNT的性质更重要。 SWCNTS官能化CN复合材料是最活跃的,其上H-2越高的H-2演化比相应的DWCNT和MWCNTS在太阳能和纯可见光光照下的相应DWCNT和MWCNTS官能化CN中最高。 PhotoCtity主要由具有通过电子顺磁共振谱的丰富和光发性电荷的丰度和稳定性连接的改进的电子特性来控制。瞬态吸收光谱验证了活性电子从CN到CNT的转移。 CNT用作电子受体改善电荷分离。数据表明,电荷转移与CNT的壁数成反比,并且通过所使用的CNT中纳米级的尺寸直接控制拍摄。在CNT / CN纳米复合材料中,当使用SWCNTS时,从CN中比CN更有效地转移光生电子,为H-2产生提供更多可用电子。

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