98%
921
2 minutes
20
Graphene nanoribbons (GNRs) with atomically precise widths and edge topologies have well-defined band gaps that depend on ribbon dimensions, making them ideal for room-temperature switching applications like field-effect transistors (FETs). For effective device integration, it is crucial to optimize growth conditions to maximize GNR length and, consequently, device yield. Equally important is establishing device integration and monitoring strategies that maintain GNR quality during the transition from growth to device fabrication. Here, we investigate the growth and alignment of 9-atom-wide armchair graphene nanoribbons (9-AGNRs) on a vicinal gold substrate, Au(788), with varying molecular precursor doses (PD) and, therefore, different resulting GNR coverages. Our investigation reveals that GNR growth location on Au(788) substrate is coverage-dependent. Scanning tunneling microscopy shows a strong correlation between GNR length evolution and both PD and GNR growth location. Employing Raman spectroscopy, samples with eight different PDs were analyzed. GNR alignment improves with length, achieving near-perfect alignment with an average length of ∼40 nm for GNRs growing solely at the Au(788) step edges. To fully exploit GNR properties in device architectures, GNRs need to be transferred from their metallic growth substrate to semiconducting or insulating substrates. Upon transfer, samples with higher PD present systematically better alignment preservation and less surface disorder, attributed to reduced GNR mobility during the transfer process. Importantly, PD also affects the substrate transfer success rate, with higher success rates observed for samples with higher GNR coverages (77%) compared to lower GNR coverages (53%). Our findings characterize the important relationship between precursor dose, GNR length, alignment quality, and surface disorder during GNR growth and upon substrate transfer, offering crucial insights for the further development of GNR-based nanoelectronic devices.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11812448 | PMC |
http://dx.doi.org/10.1039/d5na00017c | DOI Listing |
Clin Gastroenterol Hepatol
September 2025
The Global NASH/MASH Council, Washington, DC, United States; Gastroenterology Section, Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia; Liver, Digestive, and Lifestyle Health Research Section, and Organ Transplant Center of Excellence, King Faisal Sp
Background And Aim: Although the clinical burden of MASH is well known, its economic burden is less well described. We estimated MASH's economic burden in several regions of the world including the US, Germany, Spain, France, Italy, and United Kingdom (UK), Japan, Saudi Arabia, and Brazil over the next two decades.
Methods: A one-year cycle Markov model projected MASH progression from 2021 to 2040, incorporating 2020 prevalent cases and annual incident cases (2021-2040).
Nanoscale Adv
August 2025
Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST Campus UAB, Bellaterra 08193 Barcelona Spain
Bottom-up on-surface synthesis has demonstrated an impressive capability to realize desired carbon nanomaterials with atomic precision, also referred to as carbon nanoarchitectures. By using chemically tailored organic building blocks, it is possible to obtain virtually any carbon nanoarchitecture, with equally tunable electronic and magnetic properties. Among all known carbon nanoarchitectures, graphene nanoribbons (GNRs) have become the most extensively studied for nanoelectronics, due to their conductive π-conjugated structure and semiconducting nature.
View Article and Find Full Text PDFNanotechnology
September 2025
Beckman Institute for Advanced Science and Technology, Urbana, IL 61801, United States of America.
Bottom-up synthesis of graphene nanoribbons (GNRs) from aryl halide precursors is often performed thermally or in-solution, without detailing the local molecular assembly or the precursor's response to electromechanics perturbation. This synthetic approach forms nanoribbons with well-defined widths and atomically precise edges, which are necessary for ensuring bandgap uniformity. However, neither on-surface nor solution-based GNR synthesis techniques adequately address the problem of positional control, which is crucial to the fabrication of GNR transistors.
View Article and Find Full Text PDFACS Appl Nano Mater
August 2025
nanotech@surfaces laboratory, Empa - Swiss Federal Laboratories for Materials Science and Technology, 8600 Dübendorf, Switzerland.
On-surface synthesis enables the fabrication of atomically precise graphene nanoribbons (GNRs) with properties defined by their shape and edge topology. While this bottom-up approach provides unmatched control over electronic and structural characteristics, integrating GNRs into functional electronic devices requires their transfer from noble metal growth surfaces to technologically relevant substrates. However, such transfers often induce structural modifications, potentially degrading or eliminating GNRs' desired functionality - a process that remains poorly understood.
View Article and Find Full Text PDFNat Chem
September 2025
nanotech@surfaces Laboratory, Empa - Swiss Federal Laboratories for Materials Science and Technology, Dübendorf, Switzerland.
Graphene nanoribbons (GNRs) with zigzag edges are promising materials for spintronic devices due to tunable bandgaps and spin-polarized edge states. Porphyrins offer complementary benefits such as desirable optoelectronic properties. Here we combine these features in a hybrid system by means of the on-surface synthesis of zigzag-edge GNRs embedded with porphyrins laterally fused along the ribbon backbone.
View Article and Find Full Text PDF