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Jeong Ha Hwang

Publications and source records attributed to Jeong Ha Hwang.

2 recordsLinked to original sources

Ultra-high vacuum Raman platform for in situ characterization of graphene nanoribbons

Atomically precise graphene nanoribbons (GNRs) exhibit tunable electronic and magnetic properties governed by edge topology and finite-size effects, which make them versatile platforms for next-generation electronic and spintronic applications. However, the unpaired pi-electrons responsible for their magnetic properties simultaneously make them highly susceptible to chemical degradation under ambient conditions. This intrinsic reactivity poses a central experimental challenge: accessing vibrational and electronic signatures of air-sensitive GNRs during synthesis and under controlled environments without breaking vacuum. Once the material has been exposed to air, standard characterization techniques would probe oxidized or chemically modified species rather than the pristine form. Here, we overcome this limitation by developing a home-built ultra-high vacuum (UHV) Raman platform designed to preserve sample integrity by preventing air exposure and to enable in situ investigation of material properties. The portable Raman vacuum suitcase (RVS) integrates temperature control and precise gas dosing, allowing direct monitoring of growth kinetics, lattice dynamics, and reactive-edge responses under well-defined thermal and chemical environments. Using this platform, we monitor the on-surface synthesis of 7- and 9-atom-wide armchair GNRs (7- and 9-AGNRs), quantify the evolution of 7-AGNR Raman modes over a wide temperature range (162-748 K), and resolve chemical changes upon controlled O2 exposure that are consistent with oxidation at the reactive zigzag sites. These results establish UHV Raman spectroscopy with the RVS as a route to accessing the intrinsic vibrational signatures of low-dimensional quantum materials under controlled environments.

cond-mat.mtrl-sci↗

Optimized Synthesis and Device Integration of Long 17-Atom-Wide Armchair Graphene Nanoribbons

Seventeen-carbon-atom-wide armchair graphene nanoribbons (17-AGNRs) are promising candidates for high-performance electronic devices due to their narrow electronic bandgap. Atomic precision in edge structure and width control is achieved through a bottom-up on-surface synthesis (OSS) approach from tailored molecular precursors in ultra-high vacuum (UHV). This synthetic protocol must be optimized to meet the structural requirements for device integration, with ribbon length being the most critical parameter. Here, we report optimized OSS conditions that produce 17-AGNRs with an average length of approximately 17 nm. This length enhancement is achieved through a gradual temperature ramping during an extended annealing period, combined with a template-like effect driven by monomer assembly at high surface coverage. The resulting 17-AGNRs are comprehensively characterized in UHV using scanning probe techniques and Raman spectroscopy. Raman measurements following substrate transfer enabled the characterization of the length distribution of GNRs on the device substrate and confirmed their stability under ambient conditions and harsh chemical environments, including acid vapors and etchants. The increased length and ambient stability of the 17-AGNRs lead to their reliable integration into device architectures. As a proof of concept, we integrate 17-AGNRs into field-effect transistors (FET) with graphene electrodes and confirm that electronic transport occurs through the GNRs. This work demonstrates the feasibility of integrating narrow-bandgap GNRs into functional devices and contributes to advancing the development of carbon-based nanoelectronics.

cond-mat.mes-hall↗