Solution‐Processable Photonic Inks of Mie‐Resonant Hollow Carbon–Silica Nanospheres

Hollow carbon–silica nanospheres that exhibit angle‐independent structural color with high saturation and minimal absorption are made. Through scattering calculations, it is shown that the structural color arises from Mie resonances that are tuned precisely by varying the thickness of the shells. Since the color does not depend on the spatial arrangement of the particles, the coloration is angle independent and vibrant in powders and liquid suspensions. These properties make hollow carbon–silica nanospheres ideal for applications, and their potential in making flexible, angle‐independent films and 3D printed films is explored.     

基于飞秒激光制备的光子晶体光纤Fabry-Perot温度传感器

提出并设计了一种基于飞秒激光在光子晶体光纤(photonic crystal fiber,PCF)中制备光纤法布里-珀罗(Fabry-Perot,F-P)传感器的方法。采用飞秒脉冲激光作为加工光源,结合放大倍率100×的物镜以及三维加工平台在PCF侧面采用逐线刻写方式进行加工。通过对飞秒激光光斑在光纤上的聚焦位置以及刻写功率进行优化,在PCF上刻写了深度均为80 μm、间隔为800 μm的两条划线,实现了周期为0.98 nm的全光纤F-P结构制备；实验中,对传感器在40~120 ℃温度范围内的光谱特性进行了测试与分析,每隔10 ℃进行一次数据采集,随着温度逐渐增加波长向长波方向漂移,通过对该采样点数据进行线性拟合,得到该测试点的波长温度灵敏度为9.73 pm/℃,拟合线性度为0.997。     

Constraint effect caused by graphene on in situ grown Gr@WO3 -nanobrick hybrid material

This work reported the abnormal constraint effect of graphene on the structural and optical properties of in situ grown Gr@WO₃ nanobrick (NB) hybrid nanomaterials. Stable hybrid Gr@WO₃ nanomaterials were synthesized through a one-step hydrothermal method, in which different graphene contents (0.1, 0.3 and 0.5 wt%) were directly introduced into the precursor solution of tungsten oxide. The existence of graphene in the nucleation phase of tungsten oxide NB decreased the crystallite size from 49.5 nm to 45.3 nm, increased the microstrain from 1.10% to 1.44% and the optical bandgap of the hybrid samples from 2.68 eV to 2.78 eV, and reduced the radiative recombination efficiency of tungsten oxide NB. The hybridization between graphene and tungsten oxide NBs was confirmed by X-ray diffraction and Raman scattering analysis. The optical properties of materials were studied based on the absorbance and diffuse reflectance spectra. In this work, we also proposed a reliable method to estimate the optical bandgap of the sample from the diffuse reflectance spectrum. These findings would introduce an alternative method of fabrication and enhance the understanding of in situ hybrid materials.     

Halogenation effect promoted low bandgap polymers based on asymmetric isoindigo unit with low energy loss

To optimize the energy levels of the structural framework of isoindigo polymers, a series of asymmetric isoindigo based low bandgap polymers with chlorine, fluorine and thiazole substituents was constructed and their optical, electrochemical and photovoltaic properties were comparatively evaluated for the impact of different substitutions. In comparison with the polymer based on 2,2'‐bithiophene and isoindigo unit (PTi) with non‐substituted bithiophene as the donor moiety, the highest occupied molecular orbital energy level for the newly synthesized polymers is significantly decreased, and in turn an improvement of the open‐circuit voltage (V_OC) is noted in the corresponding photovoltaic devices. More importantly, combined with a low bandgap of 1.32 eV, the energy losses (E_loss) could be reduced to 0.61 eV for polymer based on chlorinated 2,2'‐bithiophene and isoindigo unit (PCl). In addition, the halogen moieties are observed to be superior in device fabrication and give better values than the thiazole substituent. Both fluorinated and chlorinated polymer donors exhibited improved performance compared with the original polymer PTi. Consequently, this work not only presents the influence of different electron withdrawing substituents on the physicochemical and photovoltaic performance, but also backs the concept of how to reduce the energy loss via the heteroatom effect. © 2020 Society of Chemical Industry     

基于拓扑单向波导的电磁诱导透明效应研究

为了研究电磁诱导透明效应在拓扑单向波导中的表现，设计了一种基于磁性光子晶体的耦合谐振腔波导。通过对谐振腔位置的调控实现了具有单向性质的电磁诱导透明效应，并利用有限时域差分仿真证明了电磁诱导透明效应在单向拓扑波导中的相关特性。该研究可为拓扑波导中实现光延迟、光开关等提供参考。     

Understanding the Self-Assembly of Cellulose Nanocrystals—Toward Chiral Photonic Materials

Over millions of years, animals and plants have evolved complex molecules and structures that endow them with vibrant colors. Among the sources of natural coloration, structural color is prominent in insects, bird feathers, snake skin, plants, and other organisms, where the color arises from the interaction of light with nanoscale features rather than absorption from a pigment. Cellulose nanocrystals (CNCs) are a biorenewable resource that spontaneously organize into chiral nematic liquid crystals having a hierarchical structure that resembles the Bouligand structure of arthropod shells. The periodic, chiral nematic organization of CNC films leads them to diffract light, making them appear iridescent. Over the past two decades, there have been many advances to develop the photonic properties of CNCs for applications ranging from cosmetics to sensors. Here, the origin of color in CNCs, the control of photonic properties of CNC films, the development of new composite materials of CNCs that can yield flexible photonic structures, and the future challenges in this field are discussed. In particular, recent efforts to make flexible photonic materials using CNCs are highlighted.     

Structural,electrical, optical and dielectric properties of yttrium substituted cadmium ferrites prepared by Co-Precipitation method

The yttrium substituted cadmium ferrites having composition Cd_1-xY_xFe₂O₄ (X = 0.00, 0.125, 0.250, 0.375, 0.500) were synthesized by the co-precipitation method and sintered at 1100 °C for 6 h. Structural, morphological, electrical, optical and dielectric characteristics were explored by XRD, SEM, EDS, FTIR, I–V two probes, UV–Vis and LCR techniques.XRD results confirmed the cubic structure of spinel ferrites. A decrease in lattice constants of the prepared samples was observed with the substitution of Y ions and was attributed to the difference in ionic radii of Y³⁺ (0.95 Å) and Cd²⁺ (0.97 Å) ions. Cationic distributions, ionic radii of both tetrahedral and octahedral sites, tolerance factor, oxygen positional parameters, bond lengths, interatomic distances, positional parameters and bond length angles were calculated from XRD data. The morphology of the prepared ferrites was studied using SEM and results ratified the XRD results. EDS confirmed the presence of all inserted elements in Cd_1-xY_xFe₂O₄ composition. DC resistivity and drift mobility of soft-ferrites were found to be increased from 1.047 × 10⁸–4.822 × 10¹⁰ Ω-cm and 5.87 × 10⁻¹² – 1.045 × 10⁻¹⁴ cm²V⁻¹s⁻¹, respectively, at 523 K with yttrium content confirming the behavior of semiconductor materials. The optical band gap energy calculated from the UV–Vis pattern of the Cd_1-xY_xFe₂O₄ system was decreased from 3.6011 to 2.8153 eV. DC resistivity and optical band gaps exposed inverse relation. FTIR results revealed lower and upper-frequency absorption bands in the ranges of 419.31–417.01 cm⁻¹ and 540.95–565.70 cm⁻¹, respectively. Dielectric constant and dielectric losses were in decreasing order, while ac conductivity revealed rising behavior with increasing frequency. Results showed the potential of yttrium doped Cd nanoferrites for applications in high-frequency microwave absorbing devices.     

Engineering 2D Multifunctional Ultrathin Bismuthene for Multiple Photonic Nanomedicine

2D monoelemental nanomaterials (Xenes) have shown tremendous potential for versatile biomedical applications. Bismuth, as a heavy element in pnictogens, has acquired massive research interest due to its unique optical performance, high biocompatibility, stability, and relatively low cost. However, the utilization of 2D bismuthene in nanomedicine has not been achieved because of the difficulty in engineering bismuthene with crucial structural/compositional characteristics for satisfying strict biomedical requirements. Herein, to address this Gordian knot, a facile strategy to intercalate and delaminate Bi bulk for generating mass few-layered 2D bismuthene with high yield by employing a water molecule mediated freezing–thawing process and sodium borohydride-triggered reduction treatment is proposed. The resulting 2D bismuthene displays good optical performance in the near-infrared (NIR) biowindow and can be excited via red light for reactive oxygen species generation, enabling applications in multiple photonic cancer nanomedicine settings, including photothermal hyperthermia and photodynamic therapy. Utilizing the intrinsic desirable optical absorbance and strong X-ray attenuation of bismuthene, dual photonic therapy can be conducted under the supervision of photoacoustic/computed tomography guided multimodal imaging. This research not only offers a potential mass-production ready, cost-effective, and eco-efficient methodology for engineering 2D Xenes, but also exploits an innovative 2D bismuthene based photonic cancer nanomedicine.