On-Surface Synthesis of -Carbon Nanostructures.

Nanomaterials (Basel)

Interdisciplinary Materials Research Center, College of Materials Science and Engineering, Tongji University, Shanghai 201804, China.

Published: December 2021

The on-surface synthesis of carbon nanostructures has attracted tremendous attention owing to their unique properties and numerous applications in various fields. With the extensive development of scanning tunneling microscope (STM) and noncontact atomic force microscope (nc-AFM), the on-surface fabricated nanostructures so far can be characterized on atomic and even single-bond level. Therefore, various novel low-dimensional carbon nanostructures, challenging to traditional solution chemistry, have been widely studied on surfaces, such as polycyclic aromatic hydrocarbons, graphene nanoribbons, nanoporous graphene, and graphyne/graphdiyne-like nanostructures. In particular, nanostructures containing -hybridized carbons are of great advantage for their structural linearity and small steric demands as well as intriguing electronic and mechanical properties. Herein, the recent developments of low-dimensional -carbon nanostructures fabricated on surfaces will be summarized and discussed.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746520PMC
http://dx.doi.org/10.3390/nano12010137DOI Listing

Publication Analysis

Top Keywords

on-surface synthesis
8
-carbon nanostructures
8
carbon nanostructures
8
nanostructures
7
synthesis -carbon
4
nanostructures on-surface
4
synthesis carbon
4
nanostructures attracted
4
attracted tremendous
4
tremendous attention
4

Similar Publications

Synthesis and Characterization of a Non-planar Cyclophenylene on Au(111).

Chemistry

January 2025

Centro de Investigacion en Nanomateriales y Nanotecnologia, -, 33940, El Entrego, SPAIN.

We report the surface-assisted synthesis of a non-planar cyclophenylene derivative containing four meta- and two para- connected phenylene moieties on Au(111), via hierarchical Ullmann coupling of a 1,10-dibrominated angular [3]phenylene and subsequent C-C bond cleavage at the four-membered rings. Scanning tunneling microscopy and spectroscopy (STM/STS) were used for the characterization of its chemical structure and electronic properties. Density functional theory (DFT) calculations support the experimental observations.

View Article and Find Full Text PDF

Gas foam injection offers a viable solution to challenges faced in oil reservoirs, yet ensuring optimal foamability and stability remains a pivotal hurdle in practical field operations. This study presents a novel synthesis procedure to create silica (SiO) Janus nanoparticles (JNPs) and examines their potential to enhance gas foam stability for enhanced oil recovery (EOR) applications. Two variations of SiO JNPs were synthesized via a masking procedure, employing oleic acid and ascorbic acid within a Pickering emulsion, marking a pioneering approach.

View Article and Find Full Text PDF

We investigated the reactivity of a -dichlorovinyl-carbazole precursor in the on-surface synthesis approach. Our findings reveal that, on the Au(111) surface, the thermally-induced dehalogenation reaction led to the formation of cumulene dimers. Contrastingly, the more reactive Cu(111) surface promoted the formation of a polyheterocyclic compound exhibiting extended aromaticity.

View Article and Find Full Text PDF

Acenes are an important class of polycyclic aromatic hydrocarbons that have gained considerable attention from chemists, physicists, and material scientists, due to their exceptional potential for organic electronics. They serve as an ideal platform for studying the physical and chemical properties of sp carbon frameworks in the one-dimensional limit and also provide a fertile playground to explore magnetism in graphenic nanostructures due to their zigzag edge topology. While higher acenes up to tridecacene have been successfully generated by means of on-surface synthesis, it is imperative to extend their synthesis toward even longer homologues to comprehensively understand the evolution of their electronic ground state.

View Article and Find Full Text PDF

Atomically precise synthesis of graphene nanostructures on semiconductors and insulators has been a formidable challenge. In particular, the metallic substrates needed to catalyze cyclodehydrogenative planarization reactions limit subsequent applications that exploit the electronic and/or magnetic structure of graphene derivatives. Here, we introduce a protocol in which an on-surface reaction is initiated and carried out regardless of the substrate type.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!