Localized Surface Plasmon Resonance Research Articles

GOLD PLASMONIC ARRAY STRUCTURES FOR SENSING APPLICATIONS

This article is devoted to the theoretical study of the plasmonic properties of periodically arranged arrays of gold nanoparticles. The Comsol Multiphysics software, which is based on the finite element method, was used to build 3D numerical models for the simulation and conduct research. In this work the electric field distribution and optical characteristics of the spherical gold nanoparticles array were studied. Individual localized surface plasmon resonance modes are influenced when metallic nanoparticles are in the close proximity and as a result the electric near- fields can couple, resulting in a new hybrid mode. We mainly focused here on the investigation of two crucial questions, particularly, influences of the gap between the nanoparticles and the refractive index of the surrounding medium on the resulting optical response of the gold nanoparticles arrays. The array of periodically arragement gold nanoparticles is characterized by an enhanced local electric field between the nanoparticles, which is inversely proportional to the gap between the particles. The field strength and optical properties (reflection, transmission, and absorption) can be conveniently manipulated by changing the gap between particles. In additional, their potential applications as sensetive plasmonic sensors element have been considered. The studied structure has a significant potential for practical applications due to its wide range of the operating wavelengths and ease of the high-throughput fabrication. In the course of the study, it was established that the change in the distance between the surface of nanoparticles by 1 nm leads to a significant shift in the spectral transmission and reflection curves on the spectral range. In addition, these studies showed that an increase in the distance between the surfaces of nanoparticles leads to the decrease in the near-field interaction between gold nanoparticles in the array. Therefore, the obtained results can be successfully used in the manufacture of highly sensitive plasmon sensors with the possibility of controlling the sensitivity and the working spectral range.

Integration of Co Single Atoms and Ni Clusters on Defect-Rich ZrO2 for Strong Photothermal Coupling Boosts Photocatalytic CO2 Reduction.

We report a solvothermal method for the synthesis of an oxygen vacancy-enriched ZrO2 photocatalyst with Co single atoms and Ni clusters immobilized on the surface. This catalyst presents superior performance for the reduction of CO2 in H2O vapor, with a CO yield reaching 663.84 μmol g-1 h-1 and a selectivity of 99.52%. The total solar-to-chemical energy conversion efficiency is up to 0.372‰, which is among the highest reported values. The success, on one hand, depends on the Co single atoms and Ni clusters for both extended spectrum absorption and serving as dual-active centers for CO2 reduction and H2O dissociation, respectively; on the other hand, this is attributed to the enhanced photoelectric and thermal effect induced by concentrated solar irradiation. We demonstrate that an intermediate impurity state is formed by the hybridization of the d-orbital of single-atom Co with the molecular orbital of H2O, enabling visible-light-driven excitation over the catalyst. In addition, Ni clusters play a crucial role in altering the adsorption configuration of CO2, with the localized surface plasmon resonance effect enhancing the activation and dissociation of CO2 induced by visible-near-infrared light. This study provides valuable insights into the synergistic effect of the dual cocatalyst toward both efficient photothermal coupling and surface redox reactions for solar CO2 reduction.

Localized surface-plasmon resonance effect as a new driver of Z-scheme electron transfer in cerium dioxide–graphitic carbon nitride heterojunctions

The intersecting interface between the two semiconductors of cerium dioxide (CeO2)–graphitic carbon nitride (g-C3N4) heterojunctions, which have demonstrated excellent photocatalytic activity, inhibits the rapid compounding of the photogenerated electron–hole pairs of g-C3N4. CeO2–g-C3N4 heterojunctions with Z-scheme and type-II electron-transfer routes were prepared via calcination in argon and air atmospheres, respectively. The built-in electric field theory cannot be used to explain the presence of a type-II electron-transfer route in CeO2–g-C3N4 heterojunctions. According the femtosecond transient absorption spectra, the localized surface-plasmon resonance (LSPR) effect of CeO2 drove the Z-scheme electron transfer in CeO2–g-C3N4 heterojunctions. The CeO2–g-C3N4 heterojunction exhibited a type-II electron-transfer route when the particle size of CeO2 increased, which attenuated the LSPR effect. The CeO2–g-C3N4 heterojunction with the Z-scheme electron-transfer route exhibited 4.4 times higher degradation efficiency for bamboo pulping wastewater than g-C3N4, and this result was attributed to the reduced complexation of photogenerated electron–hole pairs and extended photogenerated electron lifetime. Overall, this research provides a new idea for constructing Z-scheme electron-transfer heterojunctions.

Polarization-Addressable Optical Movement of Plasmonic Nanoparticles and Hotspot Spin Vortices

Spin–orbit coupling in nanoscale optical fields leads to the emergence of a nontrivial spin angular momentum component, transverse to the orbital momentum. In this study, we initially investigate how this spin–orbit coupling effect influences the dynamics in gold monomers. We observe that localized surface plasmon resonance induces self-generated transverse spin, affecting the trajectory of the nanoparticles as a function of the incident polarization. Furthermore, we investigate the spin–orbit coupling in gold dimers. The resonant spin momentum distribution is characterized by the unique formation of vortex and anti-vortex spin angular momentum pairs on opposite surfaces of the nanoparticles, also affecting the particle motion. These findings hold promise for various fields, particularly for the precision control in the development of plasmonic thrusters and the development of metasurfaces and other helicity-controlled system aspects. They offer a method for the development of novel systems and applications in the realm of spin optics.

Synthesis of Structure-Adjustable R-Au/Pt-CdS Nanohybrids with Strong Plasmon Coupling and Improved Photothermal Conversion Performance

Noble metal nanomaterials with a localized surface plasmon resonance effect exhibit outstanding advantages in areas such as photothermal therapy and photocatalysis. As a unique plasmonic metal nanostructure, gold nanobipyramids have been attracting much interest due to their strong specific local electric field intensity, large optical cross sections, and high refractive index sensitivity. In this study, we propose a novel three-component hetero-nanostructure composed of rough gold nanobipyramids (R-Au NBPs), Pt, and CdS. Initially, purified gold nanobipyramids are regrown to form R-Au NBPs that have a certain degree of roughness. These R-Au NBP substrates with a rough surface provide more hotspots and strengthen the intensity of localized electric fields. Subsequently, Pt and CdS nanoparticles are selectively deposited onto the surface of R-Au NBPs. Pt nanoparticles can provide more active sites. Each component of this hetero-nanostructure directly contacts others, creating multiple electron transfer channels. This novel design allows for tunable localized plasmon resonance wavelengths ranging from the visible to near-infrared regions. These factors contribute to the final superior photothermal conversion performance of the R-Au/Pt-CdS nanohybrids. Under the irradiation of near-infrared light (1064 nm), the photothermal conversion efficiency of R-Au/Pt-CdS reached 38.88%, which is 4.49, 1.5, and 1.22 times higher than that of Au NBPs, R-Au NBPs, and R-Au NBPs/Pt, respectively.

High-efficient water splitting over an in-situ growth novel electrocatalyst of metal-organic framework-based nanostructures

Metal-organic frameworks (MOFs) as emerging material have drawn much attention to apply to the field of water splitting. In this paper, layered NiFe-MIL-53 and nanoflower-like CoFe-MOF-74 were sequentially grown on nickel foam through two-step in-situ growth to construct a MOF-74/MIL-53 heterojunction. On this basis, we used the localized surface plasmon resonance (LSPR) effect of gold nanoparticles (Au NPs) to significantly improve the oxygen evolution reaction performance of MOF-74/MIL-53 heterojunction. Under illumation, the obtained Au-MOF-74/MIL-53 exhibits a lower overpotential of 218 mV, which is far superior to commercial catalyst. The reaction kinetics are significantly enhanced due to the lower charge transfer resistance and the higher electric double layer capacitance. We confirmed the existence of charge transfer between Au NPs and MOFs, and at the same time, the deposition of Au NPs significantly reduced the charge transfer resistance of MOF-74/MIL-53. On the basis of our work, we provide a novel MOF-based electrocatalytic nanocomposite structure for efficient water splitting.

Constructing interface chemical coupling S-scheme heterojunction MoO3-x@PPy for enhancing photocatalytic oxidative desulfurization performance: Adjusting LSPR effect via oxygen vacancy engineering

Construction of photocatalyst that combines excellent electron transfer and photoresponse capabilities to enhance photocatalytic performance remains a challenging task. In this work, interfacial Mo-N bonds and vacancy engineering collaborative modified MoO3-x@polypyrrole (MP) S-scheme heterojunction is rational designed for efficient photocatalytic oxidative desulfurization. The addition of polypyrrole introduces rich defects which inducing the localized surface plasmon resonance (LSPR) effect and enhancing light absorption. Furthermore, the combination facilitates the formation of Mo-N bonds. The modifications amplify the built-in electric field and conduct the efficacious separation of photogenerated carriers. With the synergism of LSPR effect and interfacial chemical Mo-N bonds, the optimal MP photocatalyst displays attractive desulfurization rate of 100% for dibenzothiophene (DBT) in 60 min under illumination, touching the objective of ultra-deep desulfurization. The study extends a novel understanding of the impact of LSPR effect and heterojunction interface charge transfer on the photocatalytic desulfurization ability.

Optofluidic SERS based on Ag nanocubes with high sensitivity for detecting a prevalent water pollutant

To enhance the integration and practical applicability of the Raman detection system, silver nanocubes (Ag NCs) were synthesized using a polyol method. A liquid–liquid interface approach was employed to transfer a monolayer of Ag NCs “film” onto a SiO2 substrate, resulting in the fabrication of a highly sensitive and uniform surface-enhanced Raman scattering (SERS) substrate denoted as “Ag NCs@SiO2.” The electromagnetic field distribution of various dimers on the Ag NCs@SiO2 was analyzed using finite difference time domain (FDTD) software. The results reveal that the electromagnetic enhancement effect is most pronounced in cube-cube dimers, indicating that Ag NCs exhibit superior localized surface plasmon resonance (LSPR) response due to their well-defined geometric regularity and sharp geometric angles. For Rhodamine 6G (R6G) probe molecules, the Ag NCs@SiO2 shows ultrahigh sensitivity, with a limit of detection (LOD) of 10−12 mol/L, and the enhancement factor (EF) can reach 1.4 × 1010. The relative standard deviation (RSD) at the main characteristic peaks is below 10%, demonstrating good consistency in substrate performance. In addition, the Ag NCs@SiO2 modified with hexanethiol exhibits high sensitivity, uniformity, and repeatability in detecting for pyrene, with the LOD of 10−8 mol/L and a minimum RSD of 6.09% at the main characteristic peak, and effective recognition capabilities for pyrene and anthracene in mixed solutions. Finally, chemisorption and physisorption strategies were prepared in optofluidic channels and experimentally compared, enabling real-time detection of the pyrene solution. This method can achieve a rapid detection and precise differentiation of polycyclic aromatic hydrocarbons in a water pollutant.

Localized surface plasmon resonance and atomic force microscopy study of model lipid membranes and their interactions with amyloid and melatonin

Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the accumulation of amyloid plaques in the brain. The toxicity of amyloid to neuronal cell surfaces arises from interactions between small intermediate aggregates, namely amyloid oligomers, and the cell membrane. The nature of these interactions changes with age and disease progression. In our previous work, we demonstrated that both membrane composition and nanoscale structure play crucial roles in amyloid toxicity, and that membrane models mimicking healthy neuron were less affected by amyloid than model membranes mimicking AD neuronal membranes. This understanding introduces the possibility of modifying membrane properties with membrane-active molecules, such as melatonin, to protect them from amyloid-induced damage. In this study, we employed atomic force microscopy and localized surface plasmon resonance to investigate the protective effects of melatonin. We utilized synthetic lipid membranes that mimic the neuronal cellular membrane at various stages of AD and explored their interactions with amyloid-β (1–42) in the presence of melatonin. Our findings reveal that the early diseased membrane model is particularly vulnerable to amyloid binding and subsequent damage. However, melatonin exerts its most potent protective effect on this early-stage membrane. These results suggest that melatonin could act at the membrane level to alleviate amyloid toxicity, offering the most protection during the initial stages of AD.

Novel Strategy towards Efficiency Enhancement of Flexible Optoelectronic Devices with Engineered M13 Bacteriophage

Plasmonic nanostructures, which exhibit notable localized surface plasmon resonance (LSPR) properties, are a promising approach for improving the efficiency of fiber‐shaped dye‐sensitized solar cells (FDSSCs) and flexible organic light‐emitting diodes (FOLEDs). Herein, novel plasmonic nanostructure is successfully synthesized via the self‐densification of gold nanoparticles (Au NPs) onto a genetically engineered M13 bacteriophage template. The synthesized Au NP‐M13 bio‐nanostructure show extraordinary gap‐plasmon effects and significantly enhanced LSPR properties compared to randomly dispersed Au NPs for both solid‐state FDSSCs (SS‐FDSSCs) and FOLEDs. Briefly, a power conversion efficiency (PCE) increment of 40.7% is recorded for the Au metallic NPs‐anchored M13 bacteriophage (Au NPs‐M13) enhanced SS‐FDSSCs; whereas an external quantum efficiency (EQE) increment of 47.2% is achieved for the Au NPs‐M13 enhanced FOLEDs.

Correlation between Plasmonic and Thermal Properties of Metallic Nanoparticles

Here, we investigate the correlation between the heat generated by gold nanoparticles, in particular nanospheres and nanobipyramids, and their plasmonic response manifested by the presence of Localized Surface Plasmon Resonances (LSPRs). Using a tunable laser and a thermal camera, we measure the temperature increase induced by colloidal nanoparticles in an aqueous solution as a function of the excitation wavelength in the optical regime. We demonstrate that the photothermal performances of the nanoparticles are strongly related not only to their plasmonic properties but also to the size and shape of the nanoparticles. The contribution of the longitudinal and transversal modes in gold nanobipyramids is also analyzed in terms of heat generation. These results will guide us to design appropriate nanoparticles to act as efficient heat nanosources.

High-Efficiency Ag-Modified ZnO/g-C3N4 Photocatalyst with 1D-0D-2D Morphology for Methylene Blue Degradation

Photocatalysts with different molar ratios of Ag-modified ZnO to g-C3N4 were prepared through an electrostatic self-assembly method and characterized through techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. The resulting Ag-ZnO/g-C3N4 photocatalysts exhibited a unique 1D-0D-2D morphology and Z-type heterojunction. Moreover, g-C3N4 nanosheets with large layer spacing were prepared using acid treatment and thermal stripping methods. The Z-type heterostructure and localized surface plasmon resonance effect of Ag nanowires enabled high-speed electron transfer between the materials, while retaining large amounts of active substances, and broadened the light response range. Because of these features, the response current of the materials improved, and their impedance and photoluminescence reduced. Among the synthesized photocatalysts, 0.05Ag-ZnO/g-C3N4 (molar ratio of g-C3N4/ZnO: 0.05) exhibited the highest photocatalytic performance under UV–visible light. It degraded 98% of methylene blue in just 30 min, outperforming both g-C3N4 (21% degradation in 30 min) and Ag-ZnO (84% degradation in 30 min). In addition, 0.05Ag-ZnO/g-C3N4 demonstrated high cycling stability.

Miniature computational spectrometer with a plasmonic nanoparticles-in-cavity microfilter array

Optical spectrometers are essential tools for analysing light‒matter interactions, but conventional spectrometers can be complicated and bulky. Recently, efforts have been made to develop miniaturized spectrometers. However, it is challenging to overcome the trade-off between miniaturizing size and retaining performance. Here, we present a complementary metal oxide semiconductor image sensor-based miniature computational spectrometer using a plasmonic nanoparticles-in-cavity microfilter array. Size-controlled silver nanoparticles are directly printed into cavity-length-varying Fabry‒Pérot microcavities, which leverage strong coupling between the localized surface plasmon resonance of the silver nanoparticles and the Fabry‒Pérot microcavity to regulate the transmission spectra and realize large-scale arrayed spectrum-disparate microfilters. Supported by a machine learning-based training process, the miniature computational spectrometer uses artificial intelligence and was demonstrated to measure visible-light spectra at subnanometre resolution. The high scalability of the technological approaches shown here may facilitate the development of high-performance miniature optical spectrometers for extensive applications.

Angle-Resolved Polarimetry with Quasi-Bound States in the Continuum Plasmonic Metamaterials via 3D Aerosol Nanoprinting.

Three-dimensional (3D) plasmonic metamaterials, featuring well-arranged subwavelength nanostructures, facilitate effective coupling between electrical dipoles and incident electromagnetic waves. This coupling allows for unique optical responses including localized surface plasmon resonance (LSPR) and quasi-bound states in the continuum (q-BIC). While 3D plasmonic metamaterials with LSPR and q-BIC have been independently explored for sensors, achieving simultaneous optical responses in the near-infrared region remains challenging. Here, we present 3D plasmonic metamaterials that integrate LSPR and q-BIC within a single π-shaped plasmonic structure, fabricated using a 3D aerosol nanoprinting technique. This printing technique controls the local electrostatic field to precisely position charged metallic nanoaerosols, enabling parallel printing of π-shaped plasmonic structures under ambient conditions. The printed π-shaped plasmonic structures exhibit two distinct optical modes: x-polarization-sensitive LSPR and transverse magnetic mode-sensitive q-BIC within the near-infrared region. Exploiting these dual optical responses, we demonstrate simultaneous polarization detection and incident angle analysis by integrating the π-shaped plasmonic structures into commercial Fourier-transform infrared spectroscopy, termed "numerical aperture-detective polarimetry". This approach holds promise for evaluating alignment in optical and imaging systems with light distribution analysis. Furthermore, the 3D aerosol nanoprinting technique provides an avenue for fabricating 3D plasmonic metamaterials with intricate geometries and optical properties, expanding their potential applications in nano-optics.

Numerical investigation of SERS effects of silver dimers based on homo and hybrid nanoparticles

In this study, we examine Surface-enhanced Raman Scattering effects of silver nanoparticle dimers made of sphere-sphere, sphere-cube, and sphere-cylinder topologies by utilizing the Finite-Difference-Time-domain method. We aim to elucidate the complex effects of morphology, size, and interstitial distance on the absorbance and electric field enhancement associated with localized surface plasmon resonance. Our findings show that the sphere-cube hybrid dimer gives a better possibility for enhanced field strength at the hot spot and also offers an improved absorption coefficient with a reduced full-with at half maximum.

Numerical demonstration of an efficient up-conversion enhancement strategy by plasmon excitations in a gap-mode nanocavity

Lanthanide-doped up-conversion nanoparticles (UCNPs) can be widely used as near-infrared absorbing photoactive materials in bioimaging and photovoltaic devices. However, the low absorption cross section and low luminescence quantum rate of UCNPs significantly limit its use. Therefore, a hexagonal gold pillar nano-array structure consisting of UCNPs, gold pillar arrays, gold film and silica layer is proposed. By optimizing the structural parameters, the surface plasmon resonance wavelengths are simultaneously matched with the 808 nm excitation wavelength and 450 nm emission wavelength of the UCNPs. The gap-mode nanocavity confines the incident excitation radiation to nanophotonic hotspots with greatly high field strengths, thus theoretically proposed an efficient strategy to enhance the up-conversion luminescence. The plasmonic structure investigated in this study combines the advantages of ease of processing, high absorption, low loss and good controllability of its localized surface plasmon resonance. It provides a new solution for up-conversion enhancement design of gap-mode nanocavities.

A multicolor aptasensor based on target-induced anti-etching gold nanorod for visible detection of aflatoxin B1

Foods contaminated with aflatoxin B1 (AFB1) pose a serious threat to humans, so rapid and sensitive detection of AFB1 plays an important role in public health. In this work, we developed a multicolor aptasensor based on target-mediated anti-etching of gold nanorods (AuNRs) for on-site visible detection of AFB1. The target was used as a competitor that competed with a cDNA probe labeled by horse radish peroxidase (cDNA-HRP) to bind with the aptamer coated in a microplate. The sensing mechanism was based on regulating the etching process of AuNRs upon the addition of different concentrations of AFB1. In the absence of AFB1, the AuNRs solution undergoes a distinct change from red to pink due to the etching effect of TMB2+ generated by a specific redox reaction catalyzed by the cDNA-HRP. However, in the presence of AFB1, the specific binding between AFB1 and aptamer made cDNA-HRP free out of the microplate, inhibiting the etching of AuNRs. Consequently, a redshift of longitudinal localized surface plasmon resonance (LSPR) and color alterations can be observed along with increasing the concentration of AFB1. The LSPR for visual estimation limits were 0.46 ng/mL. A good linear relationship between the wavelength shift and the concentration of AFB1 was achieved from violet to light green in the range of 1–1000 ng/mL. The established aptasensor displayed excellent detection performance, which was suitable for on-site analysis of AFB1 in actual food samples, and provided a new idea of immediate visualization detection for food hazardous factors.

Analysis of Ag-DP25/PET plasmonic nano-composites as a visible-light photocatalyst for wastewater treatment: Experimental/theoretical studies, and the DFT-MB degradation mechanism

The development of polymeric-composites Agx%DP25-PET (x = 0,1,2,3) may significantly boost the potential application of Agx%DP25 (x = 0,1,2,3) photocatalytic powders. Producing large-scale nano-composites with hybrid-surfaces, that are also flexible materials and easy to employ in a variety of environments. A set of photocatalytic nan-composites embedded with the polymeric binder poly (acrylonitrile-co-butadiene)-dicarboxy terminated (C7H9N) were performed and evaluated for wastewater treatment applications. The results reveal that the flexible polymeric composites (Agx%DP25-PET, x = 0,1,2,3) have photocatalytic activity in aqua media to degrade methylene blue (MB) under visible-light. The addition of C7H9N to immobilize photocatalytic powders on the PET surface reduces photo-generated electron-hole recombination. The materials were characterized by HR-TEM, SEM/EDX, XRD, FT-IR, UV–Vis DRS and PL. The Agx%DP25-PET (x = 0,1,2,3) photocatalytic reactions exhibited productive discoloration/degradation rates, in both aerobic (AE) and anaerobic (AN) environments. The superior photodegradation of Ag2%DP25-PET was attributed to a combination of two effects: LSPR (localized surface plasmon resonance) and Ag–TiO2/environment affinities. The findings of molecular dynamics (MD) simulation and Fukui Function (FF) based on density functional theory (DFT) provide significant insight into the photocatalytic requirements for MB discoloration/degradation. The experimental/theoretical analysis aimed to offer an in-depth understanding of medium/surface interactions on decorated TiO2 materials, as well as how these interactions affect overall degradation behavior.

Localized surface plasmon resonance (LSPR) excitation on single silver nanoring with nanoscale surface roughness

With the expansion of the application of high-sensitivity Surface-enhanced Raman scattering (SERS) technique, micro SERS-active substrates with rich optical properties and high-level functions are desired. In this study, silver nanorings with nanoscale surface roughness were fabricated as a new type of enclosed quasi-2D micro-SERS-active substrate. Highly-crystalline spherical and hemispherical silver nanoprotrusions were densely and uniformly distributed over the entire surface of the nanorings. The SERS signals were significantly enhanced on the roughened silver nanorings which were mainly derived from the maximal localized surface plasmon resonance (LSPR) points at the junctions between adjacent coupled nanoprotrusions on the roughened nanorings. The mapping image shows a uniform and intense LSPR enhancement over the nanorings, owing to the uniform and dense distribution of silver nanoprotrusions and the resulting uniform distribution of maximal LSPR points on the roughened nanorings. The dark-field spectra further indicated that the single roughened silver nanoring had significant LSPR enhancement, a wide LSPR frequency-range response, and adaptability for SERS enhancement. Notably, both the measured and simulated results demonstrate that the maximal LSPR enhancement at the junctions between the nanoprotrusions, which are distributed on the inner surface of the silver nanoring, is higher than that on the outer surface because of the plasmon-focusing effect of the enclosed silver nanoring, which leads to the lateral asymmetrical distribution of LSPR intensity, indicating more LSPR and SERS features. These results indicate that single roughened silver nanorings exhibit excellent performance as a new type of enclosed quasi-2D silver nanoring micro-SERS-active substrate, microzone LSPR catalysis, and micro/nanodevices.

Ag-modified enhance the performances of ZnO@CFs based omnidirectional photoelectrochemical ultraviolet detectors.

There are several prospective applications for omnidirectional ultraviolet (UV) detectors and underwater detection detectors in optical systems and optical fields. In this work, ZnO nanorods arrays were grown on carbon fibers (CFs). An appropriate amount of Ag nanoparticles (NPs) was deposited on the surface of ZnO nanorods by photochemical deposition. This improved the performance of photoelectrochemical (PEC) based UV detectors. Under 365 nm and 10 mW cm-2 UV irradiation, the photocurrent density of the 30s-Ag/ZnO@CFs based PEC UV detector can reach 1.28 mA cm-2, which is about 7 times that of the ZnO@CFs based PEC UV detector, and the rising time is shortened from 0.17 s to 0.10 s. The reason is that increased absorption of ultraviolet light induced by the localized surface plasmon resonance. In addition, the detector exhibits a good flexibility and remains flexible after hundreds of bends and twists. Moreover, the detector is responsive in the range of rotation angle from 0 to 360°. It provides an insight to improve the photoelectric performance and underwater omnidirectional detection ability of the PEC UV detector.