A biosensor formed by a combination of silicon (Si) micropore and graphene nanohole technology is expected to act as a promising device structure to interrogate single molecule biopolymers, such as deoxyribonucleic acid (DNA). This paper reports a novel technique of using a focused ion beam (FIB) as a tool for direct fabrication of both conical-shaped micropore in SiN/Si and a nanohole in graphene to act as a fluidic channel and sensing membrane, respectively. The thinning of thick Si substrate down to 50 µm has been performed prior to a multi-step milling of the conical-shaped micropore with final pore size of 3 µm. A transfer of graphene onto the fabricated conical-shaped micropore with little or no defect was successfully achieved using a newly developed all-dry transfer method. A circular shape graphene nanohole with diameter of about 30 nm was successfully obtained at beam exposure time of 0.1 s. This study opens a breakthrough in fabricating an integrated graphene nanohole and conical-shaped Si micropore structure for biosensor applications.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146166 | PMC |
http://dx.doi.org/10.3390/s20061572 | DOI Listing |
Nanomaterials (Basel)
September 2024
Department of Science and Engineering of Matter, Environment and Urban Planning, Marche Polytechnic University, Via Brecce Bianche, 60131 Ancona, Italy.
Nanotechnology
September 2024
Department of Electrical Engineering, The Pennsylvania State University, University Park, PA 16802, United States of America.
Engineering superlattices (SLs)-which are spatially periodic potential landscapes for electrons-is an emerging approach for the realization of exotic properties, including superconductivity and correlated insulators, in two-dimensional materials. While moiré SL engineering has been a popular approach, nanopatterning is an attractive alternative offering control over the pattern and wavelength of the SL. However, the disorder arising in the system due to imperfect nanopatterning is seldom studied.
View Article and Find Full Text PDFChem Commun (Camb)
September 2024
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng Street, Wuhan 430078, P. R. China.
FeNiSe@holey-graphene (FNS@HG) has been prepared by growth and simultaneous perforation a carbothermal reaction. The generation of nanoholes on the graphene sheets significantly reduced the diffusion distance of electrolyte ions, enhancing the rate capability of FNS@HG as an anode material for sodium-ion batteries.
View Article and Find Full Text PDFSmall
April 2024
Institut Interdisciplinaire d'Innovation Technologique (3IT), Université de Sherbrooke, 3000 Boulevard de l'Université, Sherbrooke, QC, J1K 0A5, Canada.
The heterointegration of graphene with semiconductor materials and the development of graphene-based hybrid functional devices are heavily bound to the control of surface energy. Although remote epitaxy offers one of the most appealing techniques for implementing 3D/2D heterostructures, it is only suitable for polar materials and is hugely dependent on the graphene interface quality. Here, the growth of defect-free single-crystalline germanium (Ge) layers on a graphene-coated Ge substrate is demonstrated by introducing a new approach named anchor point nucleation (APN).
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2023
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng Street, Wuhan 430078, P. R. China.
A sodium-ion battery, with a wide operating range, is much cheaper and safer than a lithium battery. Graphene is regarded as a promising carbon material in the preparation of anode materials. However, the large two-dimensional (2D) graphene sheets restrain the cross-plane diffusion of electrolyte ions, limiting the further improvement of rate performance.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!