A graphene-based long-period fiber grating (LPFG) surface plasmon resonance (SPR) sensor is proposed. A monolayer of graphene is coated onto the Ag film surface of the LPFG SPR sensor, which increases the intensity of the evanescent field on the surface of the fiber and thereby enhances the interaction between the SPR wave and molecules. Such features significantly improve the sensitivity of the sensor. The experimental results demonstrate that the sensitivity of the graphene-based LPFG SPR sensor can reach 0.344 nm%−1 for methane, which is improved 2.96 and 1.31 times with respect to the traditional LPFG sensor and Ag-coated LPFG SPR sensor, respectively. Meanwhile, the graphene-based LPFG SPR sensor exhibits excellent response characteristics and repeatability. Such a SPR sensing scheme offers a promising platform to achieve high sensitivity for gas-sensing applications.

The anisotropic plasmons properties of black phosphorus allow for realizing direction-dependent plasmonics devices. Here, we theoretically investigated the hybridization between graphene surface plasmons (GSP) and anisotropic black phosphorus localized surface plasmons (BPLSP) in the strong coupling regime. By dynamically adjusting the Fermi level of graphene, we show that the strong coherent GSP-BPLSP coupling can be achieved in both armchair and zigzag directions, which is attributed to the anisotropic black phosphorus with different in-plane effective electron masses along the two crystal axes. The strong coupling is quantitatively described by calculating the dispersion of the hybrid modes using a coupled oscillator model. Mode splitting energy of 26.5 meV and 19 meV are determined for the GSP-BPLSP hybridization along armchair and zigzag direction, respectively. We also find that the coupling strength can be strongly affected by the distance between graphene sheet and black phosphorus nanoribbons. Our work may provide the building blocks to construct future highly compact anisotropic plasmonics devices based on two-dimensional materials at infrared and terahertz frequencies.

Graphene plasmons with tightly confined fields and actively tunable resonant frequencies enable the selective detection of molecular vibrational fingerprints with ultrahigh sensitivity, significantly promoting the development of surface‐enhanced infrared absorption spectroscopies (SEIRAS). However, current experimentally obtained enhancements are much smaller than the theoretical prediction due to the extremely low graphene plasmonic mode energy. In this paper, the strategies to improve the mode energy are theoretically and experimentally investigated in a one‐port graphene plasmonic system. By optimizing the Fabry–Pérot cavity length and employing multi‐layer graphene to drive the system into the near critical coupling regime, the localized graphene plasmonic absorptions can be improved from 3% to more than 92%. This induces a 37 times improvement of graphene plasmonic mode energy from 0.4 × 10−13 to 1.5 × 10−12 J per period for the strong plasmon–molecule interactions, enabling the highly sensitive detection of 8 nm thick molecular film. The SEIRAS experimental results demonstrate that a maximum enhancement factor of 162 can be achieved, which is one order larger than that of the reported localized graphene plasmonic sensors. The results showcase the practical usability of localized graphene plasmons for the next‐generation high sensitive nanoscale infrared spectroscopy.

Ag nanoparticles (NPs) modified graphene nanoribbons (GNRs) are proposed to function as the high‐performance shared substrates for surface‐enhanced Raman and infrared absorption spectroscopy (SERS and SEIRAS). This is realized by modulating the localized plasmonic resonances of Ag NPs in visible region and GNRs in mid‐infrared region simultaneously, so as to selectively employ each resonance to acquire SERS and SEIRAS on a single substrate. As a proof of concept, shared substrates are prepared by fabricating GNRs on a Fabry–Pérot like cavity, followed by depositing a thin Ag film with annealing treatment to achieve Ag NPs. Complementary Raman and infrared active vibrational modes of rhodamine 6G molecules can be extracted from the SERS and SEIRAS spectra. By optimizing the dimension of Ag NPs, SERS enhancement factors at the order of 105 can be achieved, which are comparable with or even larger than that of the reported shared substrates. Meanwhile, various polyethylene oxide vibrational modes can be recognized with maximum SEIRAS amplification up to 170 times, which is one order larger than that of the reported graphene plasmonic infrared sensors. Such plasmonic nanosensor with excellent SERS and SEIRAS performance exhibits promising potential for biosensing applications on an integrated lab‐on‐a‐chip strategy.

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