The integration of optomechanics and optoelectronics in a single device opens new possibilities for developing information technologies and exploring fundamental phenomena. Gallium arsenide (GaAs) is a well-known material that can bridge the gap betw
een the functionalities of optomechanical devices and optical gain media. Here, we experimentally demonstrate a high-frequency GaAs optomechanical resonator with a ring-type bullseye geometry that is unprecedented in this platform. We measured mechanical modes up to 3.4 GHz with quality factors of 4000 (at 77 K) and optomechanical coupling rates up to 39 kHz at telecom wavelengths. Moreover, we investigated the material symmetry break due to elastic anisotropy and its impact on the mechanical mode spectrum. Finally, we assessed the temperature dependence of the mechanical losses and demonstrated the efficiency and anisotropy resilience of the bullseye anchor loss suppression, indicating that lower temperature operation may allow mechanical quality factors over $10^4$. Such characteristics are valuable for active optomechanics, coherent microwave-to-optics conversion via piezo-mechanics and other implementations of high-frequency oscillators in III-V materials.
The simultaneous ordering of different degrees of freedom in complex materials undergoing spontaneous symmetry-breaking transitions often involves intricate couplings that have remained elusive in phenomena as wide ranging as stripe formation, unconv
entional superconductivity or colossal magnetoresistance. Ultrafast optical, x-ray and electron pulses can elucidate the microscopic interplay between these orders by probing the electronic and lattice dynamics separately, but a simultaneous direct observation of multiple orders on the femtosecond scale has been challenging. Here we show that ultrabroadband terahertz pulses can simultaneously trace the ultrafast evolution of coexisting lattice and electronic orders. For the example of a charge-density-wave (CDW) in 1T-TiSe2, we demonstrate that two components of the CDW order parameter - excitonic correlations and a periodic lattice distortion (PLD) - respond very differently to 12-fs optical excitation. Even when the excitonic order of the CDW is quenched, the PLD can persist in a coherently excited state. This observation proves that excitonic correlations are not the sole driving force of the CDW transition in 1T-TiSe2, and exemplifies the sort of profound insight that disentangling strongly coupled components of order parameters in the time domain may provide for the understanding of a broad class of phase transitions.
The phase diagram of the one-dimensional extended Hubbard model at half-filling is investigated by a weak coupling renormalization group method applicable beyond the usual continuum limit for the electron spectrum and coupling constants. We analyze t
he influence of irrelevant momentum dependent interactions on asymptotic properties of the correlation functions and the nature of dominant phases for the lattice model under study.
