Pump-controlled RGB single-mode polymer lasers based on a hybrid 2D–3D μ-cavity for temperature sensing

Nanophotonics ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Kun Ge ◽  
Dan Guo ◽  
Ben Niu ◽  
Zhiyang Xu ◽  
Jun Ruan ◽  
...  

Abstract Single mode lasers, particularly red-green-blue (RGB) colors, have attracted wide attention due to their potential applications in the photonic field. Here, we realize the RGB single mode lasing in a hybrid two-dimension and three-dimension (2D–3D) hybrid microcavity (μ-cavity) with a low threshold. The hybrid 2D–3D μ-cavity consists of a polymer fiber and a microsphere. Typical RGB polymer film consisting gain materials are cladded on a fiber. To achieve single mode lasing, the polymer fiber therein serves as an excellent gain cavity to provide multiple lasing modes while the microsphere acts as a loss channel to suppress most of the lasing modes. Mode switching can be realized by adjusting the pump position. It can be attributed to the change of coupled efficiency between gain μ-cavity and loss μ-cavity. Our work will provide a platform for the rational design of nanophotonic devices and on-chip communication.

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Van Duong Ta ◽  
Rui Chen ◽  
Handong Sun

AbstractMicrolasers with controllable polarization of output emission are vital for on-chip optical communications, optical sensors and optical switches. In this work, we report a high quality (Q) factor, low-threshold polymer microfiber laser and the possibility of achieving laser emission with a desired polarization. The microfiber is fabricated by direct drawing from a dye-doped polymer solution and it can generate whispering gallery mode (WGM) lasing under optical pulse excitation. When the microfiber is pumped from the side with pumping direction perpendicular to the microfiber’s axis, the polarization direction of the output laser is found to be the same as that of the pump laser. Lasing emission with either transverse electric (TE) or transverse magnetic (TM) modes can be obtained and these two polarization states can be switched over by tuning the pumping laser. Furthermore, emission with both TE and TM modes can also be observed by changing the orientation of the microfiber relatively to pumping direction. Our finding provides an effective approach for achieving microlasers that have high Q lasing modes with anticipated polarization.


Nanoscale ◽  
2022 ◽  
Author(s):  
Feifei Qin ◽  
Gangyi Zhu ◽  
Junbo Yang ◽  
Lai Wei ◽  
Qiannan Cui ◽  
...  

Effective lasing mode control and unidirectional coupling of semiconductor microlasers are vital to boost their applications in optical interconnects, on-chip communication and bio-sensors. In this paper, symmetric and asymmetric GaN...


2021 ◽  
Author(s):  
Yunkai Wu ◽  
Xian Chen ◽  
Limin Jin ◽  
Xiangzhe Ai ◽  
Shumin Xiao ◽  
...  

Abstract Multi-wavelength lasing, with dynamic switching functionality, high spectral purity and contrast, plays an essential role in photonic devices. Lanthanide(Ln3+)-doped upconversion nanocrystals(UCNCs) featured with plentiful energy levels act as ideal candidates for the gain medium. However, it remains a daunting challenge to develop a tunable Ln3+-based single-mode laser across a wide wavelength range due to the absence of an appropriate mode-selection mechanism. Here, we have demonstrated the first active control of unidirectional single-mode lasing with switchable wavelength spanning beyond a record range (~ 300 nm). This is accomplished through the integration of two size-mismatched coupled microdisks cavity and inversely designed dual-mode UCNCs incorporated with selective sensitizer-pair and activator ions. By asymmetric pumping, a reversible and crosstalk-free ultraviolet-to-red single-mode operation were formed respectively from such UCNCs-based system through changing the pumping wavelengths from 980 nm to 808 nm. The results enlighten the rational design of luminescent materials and microcavity. With remarkable doping flexibility, our approach would pave an avenue to a class of UCNCs-based photonic devices for on-chip optical filter, switch, sensor and other devices.


2020 ◽  
Author(s):  
Yunzhong Wang ◽  
Saixing Tang ◽  
Yating Wen ◽  
Shuyuan Zheng ◽  
Bing Yang ◽  
...  

<div>Persistent room-temperature phosphorescence (p-RTP) from pure organics is attractive </div><div>due to its fundamental importance and potential applications in molecular imaging, </div><div>sensing, encryption, anticounterfeiting, etc.1-4 Recently, efforts have been also made in </div><div>obtaining color-tunable p-RTP in aromatic phosphors5 and nonconjugated polymers6,7. </div><div>The origin of color-tunable p-RTP and the rational design of such luminogens, </div><div>particularly those with explicit structure and molecular packing, remain challenging. </div><div>Noteworthily, nonconventional luminophores without significant conjugations generally </div><div>possess excitation-dependent photoluminescence (PL) because of the coexistence of </div><div>diverse clustered chromophores6,8, which strongly implicates the possibility to achieve </div><div>color-tunable p-RTP from their molecular crystals assisted by effective intermolecular </div><div>interactions. Here, inspirited by the highly stable double-helix structure and multiple </div><div>hydrogen bonds in DNA, we reported a series of nonconventional luminophores based on </div><div>hydantoin (HA), which demonstrate excitation-dependent PL and color-tunable p-RTP </div><div>from sky-blue to yellowish-green, accompanying unprecedentedly high PL and p-RTP </div><div>efficiencies of up to 87.5% and 21.8%, respectively. Meanwhile, the p-RTP emissions are </div><div>resistant to vigorous mechanical grinding, with lifetimes of up to 1.74 s. Such robust, </div><div>color-tunable and highly efficient p-RTP render the luminophores promising for varying </div><div>applications. These findings provide mechanism insights into the origin of color-tunable </div><div>p-RTP, and surely advance the exploitation of efficient nonconventional luminophores.</div>


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michał Dudek ◽  
Rafał Kowerdziej ◽  
Alessandro Pianelli ◽  
Janusz Parka

AbstractGraphene-based hyperbolic metamaterials provide a unique scaffold for designing nanophotonic devices with active functionalities. In this work, we have theoretically demonstrated that the characteristics of a polarization-dependent tunable hyperbolic microcavity in the mid-infrared frequencies could be realized by modulating the thickness of the dielectric layers, and thus breaking periodicity in a graphene-based hyperbolic metamaterial stack. Transmission of the tunable microcavity shows a Fabry–Perot resonant mode with a Q-factor > 20, and a sixfold local enhancement of electric field intensity. It was found that by varying the gating voltage of graphene from 2 to 8 V, the device could be self-regulated with respect to both the intensity (up to 30%) and spectrum (up to 2.1 µm). In addition, the switching of the device was considered over a wide range of incident angles for both the transverse electric and transverse magnetic modes. Finally, numerical analysis indicated that a topological transition between elliptic and type II hyperbolic dispersion could be actively switched. The proposed scheme represents a remarkably versatile platform for the mid-infrared wave manipulation and may find applications in many multi-functional architectures, including ultra-sensitive filters, low-threshold lasers, and photonic chips.


Electronics ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 346 ◽  
Author(s):  
Lili Shen ◽  
Ning Wu ◽  
Gaizhen Yan

By using through-silicon-vias (TSV), three dimension integration technology can stack large memory on the top of cores as a last-level on-chip cache (LLC) to reduce off-chip memory access and enhance system performance. However, the integration of more on-chip caches increases chip power density, which might lead to temperature-related issues in power consumption, reliability, cooling cost, and performance. An effective thermal management scheme is required to ensure the performance and reliability of the system. In this study, a fuzzy-based thermal management scheme (FBTM) is proposed that simultaneously considers cores and stacked caches. The proposed method combines a dynamic cache reconfiguration scheme with a fuzzy-based control policy in a temperature-aware manner. The dynamic cache reconfiguration scheme determines the size of the cache for the processor core according to the application that reaches a substantial amount of power consumption savings. The fuzzy-based control policy is used to change the frequency level of the processor core based on dynamic cache reconfiguration, a process which can further improve the system performance. Experiments show that, compared with other thermal management schemes, the proposed FBTM can achieve, on average, 3 degrees of reduction in temperature and a 41% reduction of leakage energy.


2017 ◽  
Vol 114 (44) ◽  
pp. 11609-11614 ◽  
Author(s):  
Alexandra M. Tayar ◽  
Eyal Karzbrun ◽  
Vincent Noireaux ◽  
Roy H. Bar-Ziv

Understanding how biochemical networks lead to large-scale nonequilibrium self-organization and pattern formation in life is a major challenge, with important implications for the design of programmable synthetic systems. Here, we assembled cell-free genetic oscillators in a spatially distributed system of on-chip DNA compartments as artificial cells, and measured reaction–diffusion dynamics at the single-cell level up to the multicell scale. Using a cell-free gene network we programmed molecular interactions that control the frequency of oscillations, population variability, and dynamical stability. We observed frequency entrainment, synchronized oscillatory reactions and pattern formation in space, as manifestation of collective behavior. The transition to synchrony occurs as the local coupling between compartments strengthens. Spatiotemporal oscillations are induced either by a concentration gradient of a diffusible signal, or by spontaneous symmetry breaking close to a transition from oscillatory to nonoscillatory dynamics. This work offers design principles for programmable biochemical reactions with potential applications to autonomous sensing, distributed computing, and biomedical diagnostics.


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