arXiv subjects

Jigang Wang

Publications and source records attributed to Jigang Wang.

42 records · Page 3Linked to original sources

arXiv2014

One- and two-dimensional photo-imprinted diffraction gratings for manipulating terahertz waves

Emerging technology based on artificial materials containing metallic structures has raised the prospect for unprecedented control of terahertz waves through components like filters, absorbers and polarizers. The functionality of these devices is static by the very nature of their metallic or polaritonic composition, although some degree of tunability can be achieved by incorporating electrically biased semiconductors. Here, we demonstrate a photonic structure by projecting the optical image of a metal mask onto a thin GaAs substrate using a femtosecond pulsed laser source. We show that the resulting high-contrast pattern of photo- excited carriers can create diffractive elements operating in transmission. With the metal mask replaced by a digital micromirror device, our photo-imprinted photonic structures provide a route to terahertz components with reconfigurable functionality.

physics.optics↗

arXiv2014

Broadband terahertz generation from metamaterials

The terahertz spectral regime, ranging from about 0.1 to 15 THz, is one of the least explored yet most technologically transformative spectral regions. One current challenge is to develop efficient and compact terahertz emitters/detectors with a broadband and gapless spectrum that can be tailored for various pump photon energies. Here we demonstrate efficient single-cycle broadband THz generation, ranging from about 0.1 to 4 THz, from a thin layer of split-ring resonators with few tens of nanometers thickness by pumping at the telecommunications wavelength of 1.5 micrometer (200 THz). The terahertz emission arises from exciting the magnetic-dipole resonance of the split-ring resonators and quickly decreases under off-resonance pumping. This, together with pump polarization dependence and power scaling of the terahertz emission, identifies the role of optically induced nonlinear currents in split-ring resonators. We also reveal a giant sheet nonlinear susceptibility $\sim$10$^{-16}$ m$^2$V$^{-1}$ that far exceeds thin films and bulk non-centrosymmetric materials.

cond-mat.mes-hall↗

arXiv2014

Ultrafast observation of critical nematic fluctuations and giant magnetoelastic coupling in iron pnictides

Many of the iron pnictides have strongly anisotropic normal-state characteristics, important for the exotic magnetic and superconducting behavior these materials exhibit. Yet, the origin of the observed anisotropy is unclear. Electronically driven nematicity has been suggested, but distinguishing this as an independent degree of freedom from magnetic and structural orders is difficult, as these couple together to break the same tetragonal symmetry. Here we use time-resolved polarimetry to reveal critical nematic fluctuations in unstrained Ba(Fe_(1-x)Co_x)_2As_2. The femtosecond anisotropic response, which arises from the two-fold in-plane anisotropy of the complex refractive index, displays a characteristic two-step recovery absent in the isotropic response. The fast recovery appears only in the magnetically ordered state, whereas the slow one persists in the paramagnetic phase with a critical divergence approaching the structural transition temperature. The dynamics also reveal a gigantic magnetoelastic coupling that far exceeds electron-spin and electron-phonon couplings, opposite to conventional magnetic metals.

cond-mat.str-el↗

arXiv2013

Transient Charge and Energy Balance in Graphene Induced by Ultrafast Photoexcitation

Ultrafast optical pump-probe spectroscopy measurement on monolayer graphene observes significant optical nonlinearities. We show that strongly photoexcited graphene monolayers with 35 fs pulses quasi-instantaneously build up a broadband, inverted Dirac fermion population. Optical gain emerges and directly manifests itself via a negative conductivity at the near-infrared region for the first 200fs, where stimulated emission completely compensates absorption loss in the graphene layer. To quantitatively investigate this transient, extremely dense photoexcited Dirac-fermion state, we construct a two-chemical-potential model, in addition to a time-dependent transient carrier temperature above lattice temperature, to describe the population inverted electronic state metastable on the time scale of tens of femtoseconds generated by a strong exciting pulse. The calculated transient optical conductivity reveals a complete bleaching of absorption, which sets the saturation density during the pulse propagation. Particularly, the model calculation reproduces the negative optical conductivity at lower frequencies in the states close to saturation, corroborating the observed femtosecond stimulated emission and optical gain in the wide near-infrared window.

cond-mat.mes-hall↗

arXiv2013

Post-transient relaxation in graphene after an intense laser pulse

High intensity laser pulses were recently shown to induce a population inverted transient state in graphene [T. Li et al. Phys. Rev. Lett. 108, 167401 (2012)]. Using a combination of hydrodynamic arguments and a kinetic theory we determine the post-transient state relaxation of hot, dense, population inverted electrons towards equilibrium. The cooling rate and charge-imbalance relaxation rate are determined from the Boltzmann-equation including electron-phonon scattering. We show that the relaxation of the population inversion, driven by inter-band scattering processes, is much slower than the relaxation of the electron temperature, which is determined by intra-band scattering processes. This insight may be of relevance for the application of graphene as an optical gain medium.

cond-mat.mes-hall↗

arXiv2010

Ultrafast Spectroscopy of Mid-Infrared Internal Exciton Transitions of Separated Single-Walled Carbon Nanotubes

We report a femtosecond mid-infrared study of the broadband low-energy response of individually separated (6,5) and (7,5) single-walled carbon nanotubes. Strong photoinduced absorption is observed around 200 meV, whose transition energy, oscillator strength, resonant chirality enhancement and dynamics manifest the observation of quasi-1D intra-excitonic transitions. A model of the nanotube 1s-2p cross section agrees well with the signal amplitudes. Our study further reveals saturation of the photoinduced absorption with increasing phase-space filling of the correlated e-h pairs.

cond-mat.mes-hall↗