To solve the phase matching and analyte filling problems in the microstructured optical fiber (MOF)-based surface plasmon resonance (SPR) sensors, we present the D-shaped hollow core MOF-based SPR sensor. The air hole in the fiber core can lower the refractive index of a Gaussian-like core mode to match with that of a plasmon mode. The analyte is deposited directly onto the D-shaped flat surface instead of filling the fiber holes. We numerically investigate the effect of the air hole in the core on the SPR sensing performance, and identify the sensor sensitivity on wavelength, amplitude and phase. This work allows us to determine the feasibility of using the D-shaped hollow-core MOFs to develop a high-sensitivity, real-time and distributed SPR sensor.
We propose a temperature sensor design based on surface plasmon resonances (SPRs) supported by filling the holes of a six-hole photonic crystal fiber (PCF) with a silver nanowire. A liquid mixture (ethanol and chloroform) with a large thermo-optic coefficient is filled into the PCF holes as sensing medium. The filled silver nanowires can support resonance peaks and the peak will shift when temperature variations induce changes in the refractive indices of the mixture. By measuring the peak shift, the temperature change can be detected. The resonance peak is extremely sensitive to temperature because the refractive index of the filled mixture is close to that of the PCF material. Our numerical results indicate that a temperature sensitivity as high as 4 nm/K can be achieved and that the most sensitive range of the sensor can be tuned by changing the volume ratios of ethanol and chloroform. Moreover, the maximal sensitivity is relatively stable with random filled nanowires, which will be very convenient for the sensor fabrication.
Graphitic carbon nitride (g-C 3 N 4 ) has been widely studied as a fascinating visible-light-response two-dimensional semiconductor photocatalyst. Nevertheless, the quantum yield of g-C 3 N 4 is unsatisfactory due to the insufficient surface reactive sites and slow charge migration efficiency caused by grievous agglomeration and large grain size. Herein this obstacle is overcome through a facile eco-friendly strategy based on effects from a bubble template and nonmetal heteroatom doping of g-C 3 N 4 . This treatment not only restricts the agglomeration but also creates more surface active sites for reaction and more porous channels for charge carrier transfer. Well-amended g-C 3 N 4 nanosheets with porous network and sulfur-doping were prepared with larger specific surface areas and faster electron−hole migration and separation capacity. The modified g-C 3 N 4 nanosheets possessed a H 2 evolution rate 5.3 and 3.8 times enhanced compare with bulk g-C 3 N 4 (BCN) and S-doped g-C 3 N 4 (CNS).
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