Flexible semiconductor nanomembranes bend into microscale scroll architectures for wide-angle infrared photodetection.

We demonstrate a dynamic axial mode tuning method by means of near-field probe in a rolled-up optical microcavity. The spatially selective nature of the tuning has been explored through both the lateral and transversal probing processes. A series of perturbation calculations based on the axial confinement model are performed to prove and improve the understanding of experimental results.

Quantum sciences are revolutionizing computing and communication technologies, in which single-photon emitters are the key components for creating strong quantum entanglement. Color centers in diamonds in coupled-cavity systems are considered great candidates for the efficient generation of quantum carriers over other solid-state emitters. Owing to the multi-mode nature of high quality factor (Q) diamond cavities, however, it is a grand challenge to the achievement of single photon emission with high rate and indistinguishability. To this end, a single-mode high-Q diamond cavity is highly desired. Here, we report a diamond mesostructured nanomembrane microcavity of a discrete rotational symmetry that selectively produces the desired single-mode emission in a broad spectrum. The strategic rolling up of a flexible diamond nanomembrane with aligned holes effectively defines the designed symmetry while maintaining the high-Q resonance through the whispering-gallery mode supported in the central hollow microcavity. The demonstrated diamond mesostructured microcavity features a distinct and enhanced single-mode emission, a step toward efficient quantum sources with designed positions or bands for quantum information technology.

The dark current characteristics and temperature dependence for quantum dot infrared photodetectors have been investigated by comparing the dark current activation energies between two samples with identical structure of the dots-in-well in nanoscale but different microscale n-i-n environments. A sequential coupling transport mechanism for the dark current between the nanoscale and the microscale processes is proposed. The dark current is determined by the additive mode of two activation energies: Ea,micro from the built-in potential in the microscale and Ea,nano related to the thermally assisted tunneling in nanoscale. The activation energies Ea,micro and Ea,nano decrease exponentially and linearly with increasing applied electric field, respectively.