Nanoscale-femtosecond dielectric response of Mott insulators captured by two-color near-field ultrafast electron microscopy

被引:37
作者
Fu, Xuewen [1 ,2 ]
Barantani, Francesco [3 ,4 ]
Gargiulo, Simone [3 ]
Madan, Ivan [3 ]
Berruto, Gabriele [3 ]
LaGrange, Thomas [3 ]
Jin, Lei [5 ]
Wu, Junqiao [5 ]
Vanacore, Giovanni Maria [6 ]
Carbone, Fabrizio [3 ]
Zhu, Yimei [2 ]
机构
[1] Nankai Univ, Sch Phys, Ultrafast Electron Microscopy Lab, Tianjin 300071, Peoples R China
[2] Brookhaven Natl Lab, Condensed Matter Phys & Mat Sci Dept, Upton, NY 11973 USA
[3] Ecole Polytech Fed Lausanne, Lab Ultrafast Microscopy & Electron Scattering LU, Inst Phys, Stn 6, CH-1015 Lausanne, Switzerland
[4] Univ Geneva, Dept Quantum Matter Phys, 24 Quai Ernest Ansermet, CH-1211 Geneva 4, Switzerland
[5] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[6] Univ Milano Bicocca, Dept Mat Sci, Via Cozzi 55, I-20121 Milan, Italy
基金
瑞士国家科学基金会;
关键词
PHOTOINDUCED PHASE-TRANSITION; RESOLUTION; DYNAMICS; SPECTROSCOPY; SCATTERING; NANOWIRES; EMISSION; LIQUID;
D O I
10.1038/s41467-020-19636-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Characterizing and controlling the out-of-equilibrium state of nanostructured Mott insulators hold great promises for emerging quantum technologies while providing an exciting playground for investigating fundamental physics of strongly-correlated systems. Here, we use two-color near-field ultrafast electron microscopy to photo-induce the insulator-to-metal transition in a single VO2 nanowire and probe the ensuing electronic dynamics with combined nanometer-femtosecond resolution (10(-21)m.s). We take advantage of a femtosecond temporal gating of the electron pulse mediated by an infrared laser pulse, and exploit the sensitivity of inelastic electron-light scattering to changes in the material dielectric function. By spatially mapping the near-field dynamics of an individual nanowire of VO2, we observe that ultrafast photo-doping drives the system into a metallic state on a timescale of similar to 150fs without yet perturbing the crystalline lattice. Due to the high versatility and sensitivity of the electron probe, our method would allow capturing the electronic dynamics of a wide range of nanoscale materials with ultimate spatiotemporal resolution.
引用
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页数:11
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