Tunable and highly sensitive temperature sensor based on graphene photonic crystal fiber

Optical fiber temperature sensors have been widely employed in enormous areas ranging from electric power industry, medical treatment, ocean dynamics to aerospace. Recently, graphene optical fiber temperature sensors attract tremendous attention for their merits of simple structure and direct power detecting ability. However, these sensors based on transfer techniques still have limitations in the relatively low sensitivity or distortion of the transmission characteristics, due to the unsuitable Fermi level of graphene and the destruction of fiber structure, respectively. Here, we propose a tunable and highly sensitive temperature sensor based on graphene photonic crystal fiber (Gr-PCF) with the non-destructive integration of graphene into the holes of PCF. This hybrid structure promises the intact fiber structure and transmission mode, which efficiently enhances the temperature detection ability of graphene. From our simulation, we find that the temperature sensitivity can be electrically tuned over four orders of magnitude and achieve up to ～ 3.34×10^-3 dB/(cm·℃) when the graphene Fermi level is ～ 35 meV higher than half the incident photon energy. Additionally, this sensitivity can be further improved by ～ 10 times through optimizing the PCF structure (such as the fiber hole diameter) to enhance the light-matter interaction. Our results provide a new way for the design of the highly sensitive temperature sensors and broaden applications in all-fiber optoelectronic devices.     

量子点单光子源的光纤耦合

半导体量子点在低温下产生谱线细锐的激子发光可制备单光子源.光纤耦合可避免低温共聚焦装置扫描定位和振动影响,是实现单光子源即插即用和组件化的关键技术.在耦合工艺上,基于微区定位标记发展出拉锥光纤与光子晶体腔或波导侧向耦合、大数值孔径锥形端面光纤与量子点样片垂直耦合等技术;然而,上述工艺需要多维度精密调节以避免柔软光纤的畸形弯曲实现对准和高效耦合.陶瓷插针或石英V槽封装的光纤无弯曲且具有大平滑端面,只要与单量子点样片对准贴合就可保证垂直收光, V槽封装的排式光纤还可通过盲对粘合避免扫描对准,耦合简单.本文在前期排式光纤粘合少对数分布Bragg反射镜(distributed Bragg reflector, DBR)微柱样片实现单光子输出基础上,经理论模拟采用多对数DBR腔提升样片垂直出光和光纤收光效率,使光纤输出单光子计数率大大提升.     

新型单模大模场红外硫系玻璃光子晶体光纤设计研究

大模场光子晶体光纤在高功率激光传输、光纤放大器、光纤激光器中的广泛应用, 使其受到研究者的广泛关注.硫系玻璃在红外波段(1–20μm)具有优良透过性能, 且具有折射率高(2.0–3.5)、声子能量低(小于350 cm^-1)、 组分可调等特性, 成为制备红外光纤的理想材料. 本文设计一种基于Ge₂₀Sb₁₅Se₆₅硫系玻璃基质的新型单模传输、低损耗、超大模场面积光子晶体光纤结构, 经理论验证其在λ =10.6 μm处基模限制损耗远低于0.1 dB/m, 高阶限制模损耗大于2 dB/m, 模场面积约为13333 μm². 关键词： 硫系玻璃 大模场面积 红外光子晶体光纤 结构设计     

全光纤量子通信系统中的高速偏振控制方案

偏振控制在光通信中是至关重要的技术, 关系着通信系统的稳定性和误码率. 本文提出一种基于双向Sagnac环工作方式的全光纤高速偏振控制方案, 通过调节环中一个光纤电光相位调制器的相位差而精确控制光场偏振方向, 并且实现了单个端口输出各种偏振态, 无需后续耦合操作. 相位控制精度为10^-3 rad, 最大消光比可达30 dB, 工作速率可达2 GHz. 由于本方案的精度、调制速度和稳定性都很高, 并采用了器件简单、成本低廉的全光纤光路, 易于集成, 在量子保密通信等光通信领域中有很好的应用前景. 关键词： 光纤偏振控制器 Sagnac环 量子通信     

一种新型高双折射光子晶体光纤特性研究

设计了一种高双折射高非线性光子晶体光纤, 采用全矢量有限元法研究了这种光纤的基模模场、双折射、非线性、有效模面积及色散特性. 数值研究发现, 减小孔间距Λ的大小, 在波长1550 nm 处, 该光纤可获得10^-2 数量级的双折射B, 比普通的椭圆保偏光纤高约两个数量级; 同时, 该光纤可获得42 W^-1·km^-1 的高非线性系数γ. 另外,分别在可见光和近红外波段出现了两个零色散波长, 在波长800–2000 nm 之间具有良好的色散平坦特性. 这种设计为获得高双折射高非线性超平坦色散光子晶体光纤提供了一种新的方法, 该光纤在偏振控制、非线性光学和色散控制方面具有广泛的应用前景. 关键词： 光子晶体光纤 高双折射 高非线性 有限元法     

Precursor Based on Polyborylborazine for BN Fiber: Preparation and Rheology Properties

A polyborylborazine precursor for hexagonal boron nitride (h-BN) was obtained by reaction of boron trichloride with methylamine and its structure was characterized by ¹¹BNMR, ¹³CNMR, ¹HNMR, and FTIR. The results show that the molecular precursor consists of borazine rings connected via a cross-linked network. The results of shear rheological tests indicated that the polymer is capable of being melt spun at moderate temperature, which implies that the structure of the molecular chains of the precursor polymer is branched. The precursor polymer was spun into a continuous polymer fiber in the melt state and then subsequently heat-treated under NH₃ up to 1000°C for conversion into BN fibers. Its surface morphology was observed by scanning electron microscopy (SEM); the fiber was free of defects and cavities.     

Self-Assembled Microfibers of Simple Amphiphilic Molecules Through a Facile Precipitation Route

One-dimensional (1D) fiber structures of simple amphiphilic molecules were prepared through a facile precipitation route. The self-assembly process was studied by ultraviolet-visible absorption and Fourier transform infrared) spectroscopy, which indicated that hydrogen bonding interactions played a role in the1D growth along the axis of the fiber. The water content, self-assembling temperature, and concentration of 1,5-bis-(1-(pyridin-2-yl)ethylidene)thiocarbonohydrazide molecules in the solution had obvious effects on the size and morphology of the self-assembled products. The formation of1D superstructures is not only of a hot subject in the process of nanoscience but also opens a new venue for conveniently controlling self-assembled structures of similar organic molecules.     

Influence of the surface morphology on the melting of polymer crystals. I. Loops of random length and adjacent reentry

A polymer crystal with a noncrystalline surface layer formed by chain loops of different lengths is considered. It is assumed that the length of each loop can be changed by longitudinal diffusion of the molecule through the crystal lattice. From the condition that the free energy of the system is minimum, the loop length distribution and the average loop length as function of temperature are calculated. In contrast to the results for loops of equal length, for the present model, a substantial thickness of the noncrystalline surface layer and a broad melting range is obtained also for the case of adjacent reentry. In order to get this result one has to take into account that even an “ideal fold” consists of at least four rigidly arranged CH2 groups in energetically unfavored conformation.     

Electron paramagnetic resonance investigation of molecular bond rupture due to ozone in deformed rubber

Electron paramagnetic resonance (EPR) provides a sensitive tool by which microscopic bond rupture can be monitored simultaneously with observations of macroscopic deformation and failure. Past techniques for studying fracture in semicrystalline polymers have been extended to investigate degradation of unfilled ruber in the presence of ozone. It was found that the rate of free radical production was linearly proportional to stretch ratio and ozone concentration and that stress relaxation and creep were not directly proportional to this production rate. The latter behavior was attributed to the particular dependence of crack density and growth on stress. It was concluded that at low strains, comparatively few surface cracks form; however, at higher strains, many more crack centers become active. Although many more surface cracks are present, they do not progress into the material as rapidly. Therefore, although more bonds were broken at higher strains and stresses, the stress relaxation rate and creep rates were not significantly increased.     

Growth of interfacial debonding in notched two-dimensional unidirectional composite under stress and displacement controls

A simplified calculation method for study of the growth of interfacial debonding between elastic fiber and elastic matrix ahead of the notch-tip in composites under displacement and stress controlled conditions was presented based on the shear lag approach in which the influences of residual stress and frictional shear stress at the debonded interface were incorporated. The calculation method was applied to a model two-dimensional composite. An outline is given of the difference and similarity in the growing behavior of the debonding between the displacement and stress controls, and of the influences of the residual stresses, frictional shear stress, the nature of the final cut component (fiber or matrix) and sample length on the debonding behavior.