We report charge transport measurements in nanoscale vertical pillar structures incorporating ultrathin layers of the organic semiconductor poly(3-hexylthiophene) (P3HT). P3HT layers with thickness down to 5 nm are gently top-contacted using wedging transfer, yielding highly reproducible, robust nanoscale junctions carrying high current densities (up to 10 A/m). Current-voltage data modeling demonstrates excellent hole injection. This work opens up the pathway towards nanoscale, ultrashort-channel organic transistors for high-frequency and high-current-density operation.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259728 | PMC |
http://dx.doi.org/10.1038/srep41171 | DOI Listing |
Sci Rep
December 2024
Division of Sustainable Development, College of Science and Engineering, Hamad Bin Khalifa University, Qatar Foundation, Doha, Qatar.
As electric vehicles gain popularity, there has been a lot of interest in supporting their continued development with the aim of enhancing their dependability, environmental advantages, and charging efficiency. The scheduling of navigation and charging for electric vehicles is among the most well-known research topics. For optimal navigation and charging scheduling, the coupled network state between the transportation and power networks must be met; moreover, the scheduling outcomes might significantly impact these networks.
View Article and Find Full Text PDFChemosphere
December 2024
Gerald May Department of Civil, Construction, and Environmental Engineering, The University of New Mexico, Albuquerque, New Mexico, 87131, United States. Electronic address:
Enhanced biological phosphorus removal (EBPR) water resource recovery facilities (WRRFs) often fail to meet phosphorus discharge permit limits, indicating a need to improve EBPR to reduce environmental phosphorus discharges. EBPR designs are largely based on the Accumulibacter polyphosphate accumulating organism (PAO) metabolism, while understudied Tetrasphaera PAOs are equally important to EBPR in many facilities worldwide. Anaerobic organic carbon competition is believed to be a key driver of EBPR reliability.
View Article and Find Full Text PDFMar Environ Res
December 2024
Shenzhen Key Laboratory of Marine Microbiome Engineering Institute for Advanced Study, Shenzhen University, Shenzhen, China. Electronic address:
The ongoing decline in seawater pH, driven by the absorption of excess atmospheric CO, represents a major environmental issue. This reduction in pH can interact with metal pollution, resulting in complex effects on marine phytoplankton. In this study, we examined the combined impacts of seawater acidification and copper (Cu) exposure on the marine diatom Phaeodactylum tricornutum.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University, Harbin 150080, PR China. Electronic address:
Photocatalytically reducing CO into high-value-added chemical materials has surfaced as a viable strategy for harnessing solar energy and mitigating the greenhouse effect. But the inadequate separation of the photogenerated electron-hole pair remains a major obstacle to CO photoreduction. Constructing heterostructure photocatalysts with efficient interface charge transfer is a promising approach to solving the above problems.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
School of Instrument and Electronics, North University of China, Taiyuan 030051, China.
In order to broaden the working voltage (1.23 V) of aqueous supercapacitors, a high-performance asymmetric supercapacitor with a working voltage window reaching up to 2.1 V is assembled using a nanorod-shaped molybdenum trioxide (MoO) negative electrode and an activated carbon (AC) positive electrode, as well as a sodium sulfate-ethylene glycol ((NaSO-EG) electrolyte.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!