Nitrogen-Functionalized Graphene Nanoflakes (GNFs:N): Tunable Photoluminescence and Electronic Structures
J. W. Chiou, Sekhar C. Ray, S. I. Peng, C. H. Chuang, B. Y. Wang, H., M. Tsai, C. W. Pao, H.-J. Lin, Y. C. Shao, Y. F. Wang, S. C. Chen, W. F., Pong, Y. C. Yeh, C. W. Chen, L.-C. Chen, K.-H. Chen, M.-H. Tsai, A. Kumar, A., Ganguly, P. Papakonstantinou, H. Yamane, N. Kosugi

TL;DR
This paper explores how nitrogen functionalization in graphene nanoflakes enhances and tunes their photoluminescence and electronic structures, enabling potential applications in optoelectronics.
Contribution
It demonstrates the ability to tailor photoluminescence in GNFs by controlling nitrogen and oxygen content, revealing the underlying electronic and bonding changes.
Findings
Enhanced photoluminescence due to increased {b1} states density
Blue shift of emission linked to nitrogen and oxygen doping
Electronic structure modifications confirmed by X-ray spectroscopy
Abstract
This study investigates the strong photoluminescence (PL) and X-ray excited optical luminescence observed in nitrogen-functionalized 2D graphene nanoflakes (GNFs:N), which arise from the significantly enhanced density of states in the region of {\pi} states and the gap between {\pi} and {\pi}* states. The increase in the number of the sp2 clusters in the form of pyridine-like N-C, graphite-N-like, and the C=O bonding and the resonant energy transfer from the N and O atoms to the sp2 clusters were found to be responsible for the blue shift and the enhancement of the main PL emission feature. The enhanced PL is strongly related to the induced changes of the electronic structures and bonding properties, which were revealed by the X-ray absorption near-edge structure, X-ray emission spectroscopy, and resonance inelastic X-ray scattering. The study demonstrates that PL emission can be…
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