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Crystalline Graphdiyne Nanosheets Produced at a Gas/Liquid or Liquid/Liquid Interface.

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TLDR
The bottom-up synthesis of all-carbon, π-conjugated graphdiyne nanosheets is described, which feature regular hexagonal domains, a lower degree of oxygenation, and uniform thickness and lateral size.
Abstract
Synthetic two-dimensional polymers, or bottom-up nanosheets, are ultrathin polymeric frameworks with in-plane periodicity. They can be synthesized in a direct, bottom-up fashion using atomic, ionic, or molecular components. However, few are based on carbon–carbon bond formation, which means that there is a potential new field of investigation into these fundamentally important chemical bonds. Here, we describe the bottom-up synthesis of all-carbon, π-conjugated graphdiyne nanosheets. A liquid/liquid interfacial protocol involves layering a dichloromethane solution of hexaethynylbenzene on an aqueous layer containing a copper catalyst at room temperature. A multilayer graphdiyne (thickness, 24 nm; domain size, >25 μm) emerges through a successive alkyne–alkyne homocoupling reaction at the interface. A gas/liquid interfacial synthesis is more successful. Sprinkling a very small amount of hexaethynylbenzene in a mixture of dichloromethane and toluene onto the surface of the aqueous phase at room temperature ...

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Citations
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Journal ArticleDOI

Emerging Two-Dimensional Nanomaterials for Electrocatalysis

TL;DR: The fundamental relationships between electronic structure, adsorption energy, and apparent activity for a wide variety of 2D electrocatalysts are described with the goal of providing a better understanding of these emerging nanomaterials at the atomic level.
Journal ArticleDOI

Anchoring zero valence single atoms of nickel and iron on graphdiyne for hydrogen evolution

TL;DR: A strategy for fabrication of ACs comprising only isolated nickel/iron atoms anchored on graphdiyne is reported, which shows high hydrogen evolution electrocatalysis activities and motivates the authors to develop a general approach in the field of single-atom transition-metal catalysis.
Journal ArticleDOI

Progress in Research into 2D Graphdiyne-Based Materials

TL;DR: GDY has recently revealed the practicality of GDY as catalyst; in rechargeable batteries, solar cells, electronic devices, magnetism, detector, biomedicine, and therapy; and for gas separation as well as water purification.
Journal ArticleDOI

Selective Molecular Separation by Interfacially Crystallized Covalent Organic Framework Thin Films

TL;DR: This work has demonstrated a bottom-up interfacial crystallization strategy to fabricate these microcrystalline powders as large-scale thin films under ambient conditions, allowing simultaneous control over crystallization and morphology of the framework structure.
Journal ArticleDOI

Graphdiyne: synthesis, properties, and applications

TL;DR: This review aims at providing a comprehensive update on the synthesis of GDY and GDY-based materials, as well as their properties, including structural, electronic, mechanical, and spectral properties, and their applications in nanotechnology.
References
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Journal ArticleDOI

Generalized Gradient Approximation Made Simple

TL;DR: A simple derivation of a simple GGA is presented, in which all parameters (other than those in LSD) are fundamental constants, and only general features of the detailed construction underlying the Perdew-Wang 1991 (PW91) GGA are invoked.
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Roll-to-roll production of 30-inch graphene films for transparent electrodes

TL;DR: The roll-to-roll production and wet-chemical doping of predominantly monolayer 30-inch graphene films grown by chemical vapour deposition onto flexible copper substrates are reported, showing high quality and sheet resistances superior to commercial transparent electrodes such as indium tin oxides.
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Architecture of graphdiyne nanoscale films

TL;DR: A methodology to generate large area graphdiyne films with 3.61 cm(2) on the surface of copper via a cross-coupling reaction using hexaethynylbenzene is demonstrated and shows conductivity of 2.516 x 10(-4) S m(-1) indicating a semiconductor property.
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Covalent organic frameworks comprising cobalt porphyrins for catalytic CO2 reduction in water

TL;DR: Modular optimization of covalent organic frameworks (COFs) is reported, in which the building units are cobalt porphyrin catalysts linked by organic struts through imine bonds, to prepare a catalytic material for aqueous electrochemical reduction of CO2 to CO.
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