Ultrafast Nanoimaging of the Photoinduced Phase Transition Dynamics in VO2

被引:92
作者
Donges, Sven A. [1 ,2 ]
Khatib, Omar [1 ,2 ]
O'Callahan, Brian T. [1 ,2 ]
Atkin, Joanna M. [3 ]
Park, Jae Hyung [4 ]
Cobden, David [4 ]
Raschke, Markus B. [1 ,2 ]
机构
[1] Univ Colorado, Dept Chem, Dept Phys, Boulder, CO 80309 USA
[2] Univ Colorado, JILA, Boulder, CO 80309 USA
[3] Univ N Carolina, Dept Chem, Chapel Hill, NC 27514 USA
[4] Univ Washington, Dept Phys, Seattle, WA 98195 USA
关键词
Nano-imaging; ultrafast spectroscopy; vanadium dioxide; s-SNOM; phase transition; METAL-INSULATOR-TRANSITION; VANADIUM DIOXIDE; LIGHT-SCATTERING; SPECTROSCOPY; DOMAINS; TIP;
D O I
10.1021/acs.nanolett.5b05313
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many phase transitions in correlated matter exhibit spatial inhomogeneities with expected yet unexplored effects on the associated ultrafast dynamics. Here we demonstrate the combination of ultrafast nondegenerate pump-probe spectroscopy with far from equilibrium excitation, and scattering scanning near-field optical microscopy (s-SNOM) for ultrafast nanoimaging. In a femtosecond near-field near-IR (NIR) pump and mid-IR (MIR) probe study, we investigate the photoinduced insulator-to-metal (IMT) transition in nominally homogeneous VO2 microcrystals. With pump fluences as high as 5 mJ/cm(2), we can reach three distinct excitation regimes. We observe a spatial heterogeneity on similar to 50-100 nm length scales in the fluence-dependent IMT dynamics ranging from <100 fs to similar to 1 ps. These results suggest a high sensitivity of the IMT with respect to small local variations in strain, doping, or defects that are difficult to discern microscopically. We provide a perspective with the distinct requirements and considerations of ultrafast spatiotemporal nanoimaging of phase transitions in quantum materials.
引用
收藏
页码:3029 / 3035
页数:7
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