Eva S. Y. Aw
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Eva S. Y. Aw has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
- Adam J. Clancy
University College London
3 shared publications - Christopher A. Howard
Department of Physics & Astronomy, University College London, London, WC1E 6BT, UK
3 shared publications - Rebecca Roisin Christine Shutt
Department of Physics and Astronomy, University College London, London, UK
3 shared publications Arjun Ashoka
Cavendish Laboratory, University of Cambridge, Cambridge, UK
2 shared publications- Hilton Barbosa de Aguiar
Laboratoire Kastler Brossel, ENS-Université PSL, CNRS, Sorbonne Université, College de France, Paris, France
2 shared publications - Loren Picco
H. H. Wills Physics Laboratory, University of Bristol, Bristol, UK
2 shared publications
Latest Publications
- Open Access
- 12 March 2025
- Published by Springer Nature in Nature
- Vol. 639 (8054) , 348-353
Magnetically and optically active edges in phosphorene nanoribbons
Nanoribbons, nanometre-wide strips of a two-dimensional material, are a unique system in condensed matter. They combine the exotic electronic structures of low-dimensional materials with an enhanced number of exposed edges, where phenomena including ultralong spin coherence times1,2, quantum confinement3 and topologically protected states4,5 can emerge. An exciting prospect for this material concept is the potential for both a tunable semiconducting electronic structure and magnetism along the nanoribbon edge, a key property for spin-based electronics such as (low-energy) non-volatile transistors6. Here we report the magnetic and semiconducting properties of phosphorene nanoribbons (PNRs). We demonstrate that at room temperature, films of PNRs show macroscopic magnetic properties arising from their edge, with internal fields of roughly 240 to 850 mT. In solution, a giant magnetic anisotropy enables the alignment of PNRs at sub-1-T fields. By leveraging this alignment effect, we discover that on photoexcitation, energy is rapidly funnelled to a state that is localized to the magnetic edge and coupled to a symmetry-forbidden edge phonon mode. Our results establish PNRs as a fascinating system for studying the interplay between magnetism and semiconducting ground states at room temperature and provide a stepping-stone towards using low-dimensional nanomaterials in quantum electronics.
- 12 March 2025
- Published by Springer Nature in Nature
- Vol. 639 (8054) , 348-353
Open AccessMagnetically and optically active edges in phosphorene nanoribbons
Nanoribbons, nanometre-wide strips of a two-dimensional material, are a unique system in condensed matter. They combine the exotic electronic structures of low-dimensional materials with an enhanced number of exposed edges, where phenomena including ultralong spin coherence times1,2, quantum confinement3 and topologically protected states4,5 can emerge. An exciting prospect for this material concept is the potential for both a tunable semiconducting electronic structure and magnetism along the nanoribbon edge, a key property for spin-based electronics such as (low-energy) non-volatile transistors6. Here we report the magnetic and semiconducting properties of phosphorene nanoribbons (PNRs). We demonstrate that at room temperature, films of PNRs show macroscopic magnetic properties arising from their edge, with internal fields of roughly 240 to 850 mT. In solution, a giant magnetic anisotropy enables the alignment of PNRs at sub-1-T fields. By leveraging this alignment effect, we discover that on photoexcitation, energy is rapidly funnelled to a state that is localized to the magnetic edge and coupled to a symmetry-forbidden edge phonon mode. Our results establish PNRs as a fascinating system for studying the interplay between magnetism and semiconducting ground states at room temperature and provide a stepping-stone towards using low-dimensional nanomaterials in quantum electronics.
- Open Access
- 27 December 2023
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 16 (4) , 1742-1750
Investigating the mechanism of phosphorene nanoribbon synthesis by discharging black phosphorus intercalation compounds
Phosphorene nanoribbons can be synthesised in by intercalation of black phosphorus with Li followed by dissolution in amides. Our result suggest that the first step does not cut the sheets to ribbons, indicating they are cut by solvent interactions.
- 27 December 2023
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 16 (4) , 1742-1750
Open AccessInvestigating the mechanism of phosphorene nanoribbon synthesis by discharging black phosphorus intercalation compounds
Phosphorene nanoribbons can be synthesised in by intercalation of black phosphorus with Li followed by dissolution in amides. Our result suggest that the first step does not cut the sheets to ribbons, indicating they are cut by solvent interactions.
- Open Access
Room Temperature Optically and Magnetically Active Edges in Phosphorene Nanoribbons
Nanoribbons - nanometer wide strips of a two-dimensional material - are a unique system in condensed matter physics. They combine the exotic electronic structures of low-dimensional materials with an enhanced number of exposed edges, where phenomena including ultralong spin coherence times, quantum confinement and topologically protected states can emerge. An exciting prospect for this new material concept is the potential for both a tunable semiconducting electronic structure and magnetism along the nanoribbon edge. This combination of magnetism and semiconducting properties is the first step in unlocking spin-based electronics such as non-volatile transistors, a route to low-energy computing, and has thus far typically only been observed in doped semiconductor systems and/or at low temperatures. Here, we report the magnetic and semiconducting properties of phosphorene nanoribbons (PNRs). Static (SQUID) and dynamic (EPR) magnetization probes demonstrate that at room temperature, films of PNRs exhibit macroscopic magnetic properties, arising from their edge, with internal fields of ~ 250 to 800 mT. In solution, a giant magnetic anisotropy enables the alignment of PNRs at modest sub-1T fields. By leveraging this alignment effect, we discover that upon photoexcitation, energy is rapidly funneled to a dark-exciton state that is localized to the magnetic edge and coupled to a symmetry-forbidden edge phonon mode. Our results establish PNRs as a unique candidate system for studying the interplay of magnetism and semiconducting ground states at room temperature and provide a stepping-stone towards using low-dimensional nanomaterials in quantum electronics.
Open AccessRoom Temperature Optically and Magnetically Active Edges in Phosphorene Nanoribbons
Nanoribbons - nanometer wide strips of a two-dimensional material - are a unique system in condensed matter physics. They combine the exotic electronic structures of low-dimensional materials with an enhanced number of exposed edges, where phenomena including ultralong spin coherence times, quantum confinement and topologically protected states can emerge. An exciting prospect for this new material concept is the potential for both a tunable semiconducting electronic structure and magnetism along the nanoribbon edge. This combination of magnetism and semiconducting properties is the first step in unlocking spin-based electronics such as non-volatile transistors, a route to low-energy computing, and has thus far typically only been observed in doped semiconductor systems and/or at low temperatures. Here, we report the magnetic and semiconducting properties of phosphorene nanoribbons (PNRs). Static (SQUID) and dynamic (EPR) magnetization probes demonstrate that at room temperature, films of PNRs exhibit macroscopic magnetic properties, arising from their edge, with internal fields of ~ 250 to 800 mT. In solution, a giant magnetic anisotropy enables the alignment of PNRs at modest sub-1T fields. By leveraging this alignment effect, we discover that upon photoexcitation, energy is rapidly funneled to a dark-exciton state that is localized to the magnetic edge and coupled to a symmetry-forbidden edge phonon mode. Our results establish PNRs as a unique candidate system for studying the interplay of magnetism and semiconducting ground states at room temperature and provide a stepping-stone towards using low-dimensional nanomaterials in quantum electronics.