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在两个溶剂界面处进行单体序列设计可实现高光活性氮化碳的合成。

Monomer sequence design at two solvent interface enables the synthesis of highly photoactive carbon nitride.

作者信息

Dolai Susmita, Karjule Neeta, Azoulay Adi, Barrio Jesús

机构信息

Department of Chemistry, Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev Beer-Sheva 8410501 Israel

出版信息

RSC Adv. 2019 Aug 20;9(45):26091-26096. doi: 10.1039/c9ra05264j. eCollection 2019 Aug 19.

Abstract

Structural modifications in carbon nitrides and related carbon-based materials have been achieved in recent years by organizing their monomers into versatile supramolecular structures that serve as reactants for the high temperature solid-state reaction. To date, the organization is usually carried out in one solvent where the building blocks must be dispersed. Here, we show the utilization of a molecule with both hydrogen bond donor and acceptor sites for constructing hydrogen bonded frameworks in interfacial systems. The chemical and electronic properties of the carbon nitride materials after calcination are strongly altered showing enhanced photocatalytic performance in different model reactions. This work shows a new large-scale pathway for the synthesis of highly photoactive carbon nitride with tailored properties and morphology by employing novel supramolecular assemblies prepared in the interface between two solvents, and furthermore opens new opportunities in the rational design of different carbon-nitrogen based materials utilizing supramolecular structures.

摘要

近年来,通过将碳氮化物及相关碳基材料的单体组织成多功能超分子结构,作为高温固态反应的反应物,实现了其结构改性。迄今为止,这种组织通常在一种溶剂中进行,其中构建单元必须分散。在此,我们展示了利用具有氢键供体和受体位点的分子在界面体系中构建氢键框架。煅烧后碳氮化物材料的化学和电子性质发生了强烈变化,在不同的模型反应中表现出增强的光催化性能。这项工作展示了一条新的大规模合成途径,通过采用在两种溶剂界面制备的新型超分子组装体来合成具有定制性质和形态的高光活性碳氮化物,此外还为利用超分子结构合理设计不同的碳氮基材料开辟了新机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2580/9070395/ff2e5562840f/c9ra05264j-s1.jpg

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