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In Situ Construction of Ag/TiO2/g-C3N4 Heterojunction Nanocomposite Based on Hierarchical Co-Assembly with Sustainable Hydrogen Evolution

机译:基于分级共组装和可持续氢释放的Ag / TiO2 / g-C3N4异质结纳米复合材料的原位构建

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摘要

The construction of heterojunctions provides a promising strategy to improve photocatalytic hydrogen evolution. However, how to fabricate a nanoscale TiO /g-C N heterostructure and hinder the aggregation of bulk g-C N using simple methods remains a challenge. In this work, we use a simple in situ construction method to design a heterojunction model based on molecular self-assembly, which uses a small molecule matrix for self-integration, including coordination donors (AgNO ), inorganic titanium source (Ti(SO ) ) and g-C N precursor (melamine). The self-assembled porous g-C N nanotube can hamper carrier aggregation and it provides numerous catalytic active sites, mainly via the coordination of Ag ions. Meanwhile, the TiO NPs are easily mineralized on the nanotube template in dispersive distribution to form a heterostructure via an N–Ti bond of protonation, which contributes to shortening the interfacial carrier transport, resulting in enhanced electron-hole pairs separation. Originating from all of the above synergistic effects, the obtained Ag/TiO /g-C N heterogenous photocatalysts exhibit an enhanced H evolution rate with excellent sustainability 20.6-fold-over pure g-C N . Our report provides a feasible and simple strategy to fabricate a nanoscale heterojunction incorporating g-C N , and has great potential in environmental protection and water splitting.
机译:异质结的构建提供了改善光催化氢释放的有前途的策略。然而,如何使用简单的方法来制造纳米级的TiO / g-C N异质结构并阻碍整体g-C N的聚集仍然是一个挑战。在这项工作中,我们使用一种简单的原位构建方法来设计基于分子自组装的异质结模型,该模型使用小分子基质进行自整合,包括配位供体(AgNO),无机钛源(Ti(SO)) )和gC N前体(三聚氰胺)。自组装的多孔g-C N纳米管可以阻碍载流子聚集,并且主要通过Ag离子的配位提供许多催化活性位。同时,TiO NPs易于在纳米管模板上矿化成分散分布,通过质子化的N-Ti键形成异质结构,这有助于缩短界面载流子传输,从而增强了电子-空穴对的分离。由于上述所有协同作用,所得的Ag / TiO / g-C N异质光催化剂显示出更高的H释放速率,其可持续性是纯g-C N的20.6倍。我们的报告提供了一种可行且简单的策略来制备包含g-C N的纳米级异质结,并且在环境保护和水分解方面具有巨大潜力。

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