Controlling light emission by engineering atomic geometries in silicon photonics.

By engineering atomic geometries composed of nearly 1000 atomic segments embedded in micro-resonators, we observe Bragg resonances induced by the atomic lattice at the telecommunication wavelength. The geometrical arrangement of erbium atoms into a lattice inside a silicon nitride (SiN) microring resonator reduces the scattering loss at a wavelength commensurate with the lattice. We confirm dependency of light emission to the atomic positions and lattice spacing and also observe Fano interference between resonant modes in the system.

Optomechanical frequency comb memory.

Typical nano-mechanical oscillator arrays exhibit a mechanical frequency distribution arising from the imprecision in the nanofabrication process, thus hindering their collective dynamics. We tailor the inhomogeneously broadened spectrum of a nano-oscillator ensemble to unravel the collective dynamics of mechanical oscillators in an optomechanical array. We show that by engineering tunable optomechanical interactions, the instantaneous phase matching between the oscillators reveals collective dynamics in the form of a photon-phonon echo excitation without the need for active frequency tuning. Using numerical simulations, we demonstrate that by controlling such collective dynamics, broadband and scalable coherent light storage can be realized. An optomechanical memory of this kind enables information storage over a wide band of wavelengths, including the telecommunications band and, importantly, can be integrated into the silicon photonic networks.

Fabrication and use of silicon hollow-needle arrays to achieve tissue nanotransfection in mouse tissue in vivo.

Tissue nanotransfection (TNT) is an electromotive gene transfer technology that was developed to achieve tissue reprogramming in vivo. This protocol describes how to fabricate the required hardware, commonly referred to as a TNT chip, and use it for in vivo TNT. Silicon hollow-needle arrays for TNT applications are fabricated in a standardized and reproducible way. In <1 s, these silicon hollow-needle arrays can be used to deliver plasmids to a predetermined specific depth in murine skin in response to pulsed nanoporation. Tissue nanotransfection eliminates the need to use viral vectors, minimizing the risk of genomic integration or cell transformation. The TNT chip fabrication process typically takes 5-6 d, and in vivo TNT takes 30 min. This protocol does not require specific expertise beyond a clean room equipped for basic nanofabrication processes.