Localized Surface Plasmon Resonance Effect Research Articles

Efficient photocatalytic degradation of perfluorooctanoic acid by bismuth nanoparticle modified titanium dioxide

Perfluorooctanoic acid (PFOA) is potentially toxic and exceptionally stable attributed to its robust CF bond, which is hard to be removed by UV/TiO2 systems. In this research, bismuth nanoparticle (Bi NP) modified titanium oxides (Bi/TiO2) were synthesized by a simple photochemical deposition-calcination method and were applied as photocatalysts for the first time to degrade PFOA. The removal rate of 50 mg/L PFOA reached 99.3 % with 58.6 % defluorination rate after 30 min of irradiation via a mercury lamp. Bi/TiO2 exhibited superior performance in PFOA degradation compared to commercial photocatalysts (TiO2, Ga2O3, Bi2O3 and In2O3). In addition, Bi/TiO2 showed high degradation activity under actual sunlight, achieved 100 % removal rate and 59.3 % defluorination rate within 2 h. Bi NPs increase the light trapping ability of Bi/TiO2 and promote the separation of photogenerated electron-hole pairs via local surface plasmon resonance (LSPR) effect, which results in more photogenerated holes (h+) and hydroxyl radicals (OH). Combined with DFT calculations and intermediate detections, the degradation reaction is initiated from the oxidation of the PFOA carboxyl group via h+, followed by the loss of the CF2 unit step by step with the participation of OH. This work presents a novel approach for the practical implementation of TiO2-based photocatalysts to achieve highly efficient photocatalytic degradation of perfluorocarboxylic acids (PFCAs).

Double S-scheme Cu2−xSe/twinned-Cd0.5Zn0.5S homo-heterojunctions with surface plasmon effects for efficient photocatalytic H2 evolution

The enhancement of charge separation and utilization efficiency in both the bulk phase and interface of semiconductor photocatalysts, as well as the expansion of light absorption range, are crucial research topics in the field of photocatalysis. To address this issue, twinned Cd0.5Zn0.5S (T-CZS) homojunctions consisting of wurtzite Cd0.5Zn0.5S (WZ-CZS) and zinc blende Cd0.5Zn0.5S (ZB-CZS) were synthesized via a hydrothermal method to facilitate the bulk-phase charge separation. Meanwhile, Cu2−xSe with localized surface plasmon resonance effect (LSPR) generated by Cu vacancies was also obtained through a hydrothermal process. Due to their opposite electronegativity, a solvent evaporation strategy was employed to combine Cu2−xSe and T-CZS by intermolecular electrostatic. After optimization, the photocatalytic hydrogen (H2) evolution rate of 5 wt% Cu2−xSe/T-CZS reached an impressive value of 60 mmol∙h−1∙g−1, which was 4.6 and 66.6 times higher than that of pure Cu2−xSe and T-CZS, respectively. Furthermore, this composites demonstrated a remarkable rate of 0.46 mmol∙h−1∙g−1 under near-infrared (NIR) wavelength (>800 nm). The enhanced performance observed in Cu2−xSe/T-CZS can be attributed to its unique and efficient double S-scheme charge transfer mechanism which effectively suppresses rapid recombination of electron-hole pairs both within the bulk phase and at the surface interfaces; this conclusion is supported by Density Functional Theory (DFT) calculations as well as electron paramagnetic resonance spectroscopy analysis. Moreover, incorporation of Cu2−xSe enables effective utilization ultraviolet visible-near infrared (UV–Vis-NIR) light by the composites while facilitating injection “hot electrons” into T-CZS for promoting photocatalytic reactions. This study provides a potential strategy for achieving efficient solar energy conversion through synergistic integration of non-stoichiometric plasmonic materials with photocatalysts with twinned-twinned structures.

In Situ Heterojunction-based PEC Sensor Coupled with LSPR for Sensitive Detection of Aflatoxin B1

To enhance the performance of photoelectrochemical (PEC) sensors, heterojunction construction is a workable technique. However, the interface defects inside the structure are often ignored. In this work, an innovative photoelectrochemical (PEC) sensor based on a “turn-off” PEC model was constructed using the synergistic effects of in situ growing heterojunction and local surface plasmon resonance (LSPR) to detect Aflatoxin B1 (AFB1) instantly. In situ heterojunctions were constructed based on bismuth-based perovskite, and the internal electric field spontaneously established during the growth process can effectively compensate for the interfacial defects and promote the separation and transfer of e−/h+ pairs. Moreover, the gold nanoparticles (Au NPs) LSPR effect can improve PEC performance by enhancing the light trapping ability of the material. The PEC sensor’s detecting area for AFB1 analysis is 10.0 fg/ml-100 ng ml−1, and the detection limit is 4.34 fg ml−1. Good stability, reproducibility, and selectivity underscore the sensor’s suitability for meeting the requirements of food quality monitoring.

Efficiency Enhancement of Organic Light-Emitting Diodes with Multifunctional Magnetic Composite Nanoparticles of Fe3O4@Au@SiO2

Multifunctional nanomaterials have been widely utilized to optimize the performances of optoelectronic devices. In this work, magnetic composite nanoparticles (NPs) of Fe3O4@Au@SiO2 are used as dopants to improve the quantum efficiency of electroluminescence of the tris-(8-hydroxyquinoline) aluminum-based organic light emitting devices (OLEDs). As a result, the performances of doped OLED (Von = 2.8 V, L = 23400 cd/m2, EQE = 1.55) are obviously boosted as compared to the control device (Von = 2.9 V, L = 19780 cd/m2, EQE = 1.27). Especially, the current efficiency of fluorescent green OLEDs can be 22.5% enhanced by simply mixing the magnetic Fe3O4@Au@SiO2 (0.5 wt‰) NPs into poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), yielding the maximum value of 4.62 cd/A. The efficiency enhancement could be attributed to the collective effects of light-scattering, localized surface plasmon resonance (LSPR) and magnetic effect induced by magnetic composite NPs.

Combination of multiple routes to enhance DSSC performance: Flower-like structure of SnO2 as photoanode and modification with Ag nanoparticle

SnO2 is an attractive photoanode material for dye-sensitized solar cells (DSSCs), but it has many drawbacks and needs to be modified. In this study, flower-like SnO2 particles are firstly prepared by a simple one-step hydrothermal synthesis method respectively, and the effect of hydrothermal reaction time on the growth of the particles is explored. The morphological and structural characterisation reveals that the flower-like particles have a larger specific surface area can provide more adsorption sites for dye molecules and are more suitable for photoanode materials. Then the optimal flower-like SnO2 particles are selected to prepare the photoanode, which is also modified with different concentrations of Ag nanoparticles to successfully introduce the localized surface plasmon resonance (LSPR) effect, and the optimal modification concentration is explored. Conformal characterisation, dye adsorption and light absorption tests revealed that the modification of Ag nanoparticles not only optimises the photoanode conformal structure and improves the dye adsorption, but also works in conjunction with the LSPR effect to improve the light absorption and utilisation, thus increasing the cell efficiency. Many cell performances of DSSC are also greatly improved due to the above work, and the optimal cell performance of DSSC is achieved when the Ag nanoparticles doping concentration is 0.03 M. Compared with the pure flower-like SnO2-based photoanode DSSC, the short-circuit current density of the best Ag nanoparticle-modified DSSC is enhanced by 28.56% to 15.80 mA/cm2, and its efficiency is improved by 20.82%–5.92%.

Atomically dispersed Ag implanted zeolitic imidazolate Frameworks-8 for Visible-Light enhanced plasmonic opto-chemical sensor

A reliable and highly sensitive gas sensor is regarded as an indispensable approach for monitoring and ensuring human health and safety. Herein, a wet-chemical synthesis strategy is developed to fabricate a Agx/ZIF-8 heterostructure, in which Ag is encapsulated in porous zeolitic imidazolate frameworks-8 (ZIF-8). The size of Ag is highly tunable and precisely controllable in the range of single atom to 50 nm. Agx/ZIF-8 samples are found to be particularly useful in gas sensors for triethylamine (TEA) detection, and their sensing performance can be further enhanced via downsizing the Ag nanoparticle (NPs) into the atomical level, thus realizing the maximum utilization of Ag element as well as achieving the most outstanding sensing performance. As a result, the optimal sample Ag(SAs-1mL)/ZIF-8 with the atomic Ag, shows relatively lower operating temperature (290 °C), high response (142), superior detection limits (0.41 ppm), and ultra-fast response/recovery time (4/15 s), which are significantly better than the sample Ag(0.5nm-0.25mL)/ZIF-8 with Ag nanoclusters (ca. 0.5–1 nm in size) and other Agx/ZIF-8 samples with larger Ag nanoparticles (range from ca. 2 nm to 50 nm in diameter). Moreover, benefiting from the localized surface plasmon resonance (LSPR) effect, the response of Ag(SAs-1mL)/ZIF-8 sensor is greatly increased by as much as 440 % when it illuminated with the 405 nm LED, where the light wavelength resonates with the plasmon frequency of Ag. This work highlights the crucial role of size effect of noble metal, proves the LSPR effect of atomic level Ag, and offering an attractive strategy to improve sensitivity and stability of gas sensors based on single atoms.

Luminescence enhancement of Y2O3 thin films based on LSPR effect of Ag nanolayers

Based on the local surface plasmon resonance effect of Ag nanolayer, the luminescence enhancement in the visible light range of multilayer thin film has been investigated combined with metal/spacer molecule/photoluminescence material structure. The luminescence enhancement effect of multilayer thin films can be improved by adjusting the spin-coating number of Ag nanolayer and SiO2 spacer in the multilayer structure. At the same time, the mechanism of enhanced luminescence has been analyzed according to the change in fluorescence lifetime. The effect of the coupling between Ag nanolayer and luminescence layer on the radiative transition rate and fluorescence quantum yield have been discussed. The up-conversion luminescence intensity of the noble metal-modified multilayer thin film can be further improved by combining the multilayer structure with sensitized layer.

Scattered Co-anchored MoS2 synergistically boosting photothermal capture and storage of phase change materials

Pristine phase change materials (PCMs) suffer from inherent deficiencies of poor solar absorption and photothermal conversion. Herein, we proposed a strategy of co-incorporation of zero-dimensional (0D) metal nanoparticles and two-dimensional (2D) photothermal materials in PCMs for efficient capture and conversion of solar energy into thermal energy. Highly scattered Co-anchored MoS2 nanoflower cluster serving as photon and phonon triggers was prepared by in-situ hydrothermal growth of ZIF67 polyhedron on 2D MoS2 and subsequent high-temperature carbonization. After encapsulating thermal storage unit (paraffin wax), the obtained composite PCMs integrated high-performance photothermal conversion and thermal energy storage capability. Benefiting from the synergistic enhancement of 0D Co nanoparticles with localized surface plasmon resonance effect, carbon layer with the conjugation effect and 2D MoS2 with strong solar absorption, composite PCMs exhibited a high photothermal conversion efficiency of 95.19%. Additionally, the resulting composite PCMs also demonstrated long-term thermal storage stability and durable structural stability after 300 thermal cycles. The proposed collaborative co-incorporation strategy provides some innovative references for developing next-generation photothermal PCMs in solar energy utilization.

In Situ Construction of Interface with Photothermal and Mutual Catalytic Effect for Efficient Solar-Driven Reversible Hydrogen Storage of MgH2.

Hydrogen storage in MgH2 is an ideal solution for realizing the safe storage of hydrogen. High operating temperature, however, is required for hydrogen storage of MgH2 induced by high thermodynamic stability and kinetic barrier. Herein, flower-like microspheres uniformly constructed by N-doped TiO2 nanosheets coated with TiN nanoparticles are fabricated to integrate the light absorber and thermo-chemical catalysts at a nanometer scale for driving hydrogen storage of MgH2 using solar energy. N-doped TiO2 is in situ transformed into TiNxOy and Ti/TiH2 uniformly distributed inside of TiN matrix during cycling, in which TiN and Ti/TiHx pairs serve as light absorbers that exhibit strong localized surface plasmon resonance effect with full-spectrum light absorbance capability. On the other hand, it is theoretically and experimentally demonstrated that the intimate interface between TiH2 and MgH2 can not only thermodynamically and kinetically promote H2 desorption from MgH2 but also simultaneously weaken Ti─H bonds and hence in turn improve H2 desorption from the combination of weakened Ti─H and Ti─H bonds. The uniform integration of photothermal and catalytic effect leads to the direct action of localized heat generated from TiN on initiating the catalytic effect in realizing hydrogen storage of MgH2 with a capacity of 6.1wt.% under 27 sun.

Interfacial Bonding Induced Charge Transfer in Two-dimensional Amorphous MoO3-x/Graphdiyne Oxide Non-van der Waals Heterostructures for Dominant SERS Enhancement.

Two-dimensional semiconductor-based nanomaterials have shown to be an effective substrate for Surface-enhanced Raman Scattering (SERS) spectroscopy. However, the enhancement factor (EF) tends to be relatively weak compared to that of noble metals and does not allow for trace detection of molecules. In this work, we report the successful preparation of two-dimensional (2D) amorphous non-van der Waals heterostructures MoO3-x/GDYO nanomaterials using supercritical CO2. Due to the synergistic effect of the localized surface plasmon resonance (LSPR) effect and the charge transfer effect, it exhibits excellent SERS performance in the detection of methylene blue (MB) molecules, with a detection limit as low as 10-14M while the enhancement factor (EF) can reach an impressive 2.55 × 1011. More importantly, the chemical bond bridging at the MoO3-x/GDYO heterostructures interface can accelerate the electron transfer between the interfaces, and the large number of defective surface structures on the heterostructures surface facilitates the chemisorption of MB molecules. And the charge recombination lifetime can be proved by a ~1.7-fold increase during their interfacial electron-transfer process for MoO3-x/GDYO@MB mixture, achieving highly sensitive SERS detection.

Synergistic Densification in Hybrid Organic‐Inorganic MXenes for Optimized Photothermal Conversion

AbstractOptimizin the efficient light‐trapping in the photothermal conversion by enhancing localized surface plasmon resonance (LSPR) is crucial in improving light‐heat‐conversion efficiency of Ti3C2Tx MXene. However, its susceptibility to oxidation makes it prone to oxides formation, diminishing its metallic properties and significantly reducing the LSPR effect. This work synthesizes a kind of air‐stable hybrid Ti3C2Tx MXenes by a synergistic densification strategy that incorporates sulfhydryl‐bonding between organic and inorganic parts by reacting Ti3C2Tx MXene with thiocarboxylic acids. The resultant shortening of electron transport pathways, enhanced charge density, and the generation of additional electronic states around the Fermi level collectively contribute to an augmented LSPR effect. Additionally, the hybrid Ti3C2Tx MXenes also demonstrate high‐temperature resistance and reduced water interactions. These combined effects substantially elevate photothermal conversion efficiency through thiocarboxylic acids modification, reaching a photothermal evaporation rate of 1.77 kg m−2 h−1 with 94.56% efficiency in hybrid Ti3C2Tx MXenes. The approach paves the way for the design and development of a three‐in‐one strategy for photothermal conversion.

Construction of Au-modified CN-based donor-acceptor system coupled with dual photothermal effects for efficient photoreduction of carbon dioxide

Conversion of CO2 into high value-added fuels through the photothermal effect is an effective approach for utilizing solar energy. In this study, we prepared the CN-based photocatalyst Py-CTN-Au with both donor-acceptor (D-A) system and dual photothermal effects using a simple two-step method involving calcination and photo-deposition. Real-time monitoring with a thermal imaging camera revealed that Py-CTN-Au0.5 achieved a maximum stable temperature of 180 °C, which was approximately 1.2 times higher than that of Py-CTN (155 °C) and 1.9 times higher than that of g-CN (95 °C) under the same reaction conditions. Under the optimized reaction conditions, Py-CTN-Au0.5 exhibited a CO release rate of 30.59 umol g−1 after 4 h of reaction, which was 7.3 times higher than that of pure g-CN (4.18 umol g−1). The D-A system not only facilitated the separation and transformation of charge carriers but also induced a photothermal effect to accelerate the photoreduction of CO2. Additionally, the cocatalyst Au nanoparticles (Au NPs) further enhanced the charge carrier dynamics and photothermal effect by increasing the built-in electric field intensity and localized surface plasmon resonance (LSPR) effect, respectively. The dual photothermal effects resulting from the non-radiative photon conversion of the D-A structure and the Au NPs LSPR effect, along with the enhanced charge carrier dynamics, catalyzed the efficient photoreduction of CO2. DFT simulations were used to confirm the effect of D-A system and Au NPs. In-situ FTIR results demonstrated that the synergistic photothermal effect promoted the formation of the key intermediate species COOH*, which is beneficial for the photocatalytic reduction of CO2. This study provides valuable insights into the multiple photothermal synergistic effects in photocatalytic reactions.

Efficient Photothermal Catalytic Oxidation Enabled by Three-Dimensional Nanochannel Substrates.

Photothermal catalysis exhibits promising prospects to overcome the shortcomings of high-energy consumption of traditional thermal catalysis and the low efficiency of photocatalysis. However, there is still a challenge to develop catalysts with outstanding light absorption capability and photothermal conversion efficiency for the degradation of atmospheric pollutants. Herein, we introduced the Co3O4 layer and Pt nanoclusters into the three-dimensional (3D) porous membrane through the atomic layer deposition (ALD) technique, leading to a Pt/Co3O4/AAO monolithic catalyst. The 3D ordered nanochannel structure can significantly enhance the solar absorption capacity through the light-trapping effect. Therefore, the embedded Pt/Co3O4 catalyst can be rapidly heated and the O2 adsorbed on the Pt clusters can be activated to generate sufficient O2- species, exhibiting outstanding activity for the diverse VOCs (toluene, acetone, and formaldehyde) degradation. Optical characterization and simulation calculation confirmed that Pt/Co3O4/AAO exhibited state-of-the-art light absorption and a notable localized surface plasmon resonance (LSPR) effect. In situ diffuse reflectance infrared Fourier transform spectrometry (in situ DRIFTS) studies demonstrated that light irradiation can accelerate the conversion of intermediates during toluene and acetone oxidation, thereby inhibiting byproduct accumulation. Our finding extends the application of AAO's optical properties in photothermal catalytic degradation of air pollutants.

Photoelectric dual-mode triggered phase change materials for all-weather personal thermal management and shape memory

To cope with the demand of more complex and variable applications, it is urgent to develop dual-mode triggered, breathable, and shape-memory wearable heaters for all-weather personal thermal management of composite phase change materials (PCMs). Herein, after high-temperature carbonization of ZnCo-MOF (metal–organic framework) nanosheet array grown in situ on flexible and breathable carbon cloth (CC) and subsequent encapsulation of polyethylene glycol (PEG), the as-prepared PEG/CC@Co/CNT (carbon nanotube) composite PCMs exhibited good breathability, mechanical strength (tensile strength of 9.15 MPa), thermal energy storage density (114.19 J/g), and shape memory due to the synergy of flexible CC skeleton and rigid PEG. More importantly, composite PCMs possessed excellent solar-thermal (93.7 %, 100 mW/cm2) and electro-thermals (94.5 %, 2.0 V) conversion and storage capacity, benefiting from the conjugation effect of high graphitized carbon/carbon heterostructure with fast electron/photon/phonon transmission and the localized surface plasmon resonance effect of Co nanoparticles. Therefore, the integration of solar heating and Joule heating into breathable composite PCMs can be accurately used for next-generation all-weather, all-season, dual-mode triggered personal thermal management, including indoor/outdoor, daytime/night, rainy/cloudy and other complex and changeable scenarios.

Effects of Plasmonic Au Nanoparticles on the Optical Nonlinearity of InAs/GaAs Quantum Dot Semiconductor Saturable Absorber Mirrors

Au nanoparticles (NPs) were designed to be embedded into III-V semiconductors to form Au/GaAs Schottky heterostructures, which were used as top-modified cover layers for quantum dot semiconductor saturable absorption mirrors (QD-SESAMs). By harnessing the distinctive localized surface plasmon resonance (LSPR) effect exhibited by Au NPs, a remarkable enhancement in photogenerated carrier concentration is achieved at the heterojunction interface. Consequently, this leads to a significant improvement in the nonlinear optical characteristics of the device. The modulation depth (MD) and saturation fluence of the device are optimized from the initial 2.2% and 16.1 MW/cm2 to 2.8% and 8.3 MW/cm2, respectively. Based on the optimized device, a Q-switched laser has been developed with an impressive output power of 17.61 mW and a single pulse energy of 274.9 nJ. These results unequivocally showcase the exceptional advantages offered by utilizing Au NPs to optimize the nonlinear optical characteristics of III-V semiconductor devices, thereby highlighting its immense potential for practical applications in various fields.

Construction of medium-entropy alloys coupled Z-Scheme heterojunction and its enhanced photocatalytic performance by regulating mechanism of LSPR effect

Optimizing the local surface plasmon resonance (LSPR) effect of non-noble metals through alloying has been crucial for improving its practical application in the field of photocatalysis. Rare studies capture the detail that the change in the electronic structure of metal elements caused by alloying affects plasma carrier concentration and the local surface plasmon resonance effect. Herein, NiCuCoFe medium-entropy alloys (MEAs) nanoclusters were designed and used to modify the Bi3O4Br/CNNs Z-scheme heterojunction. The cocktail effect of MEAs causes the 3d-orbital hybridization of various metal elements, which promotes the release of charge carriers. The higher the carrier concentration, the stronger the LSPR effect of MEAs. In addition, the mechanism of three typical working pathways of the LSPR effect to improve the photocatalytic performance of heterojunction is discussed. And compared with those of Bi3O4Br, CNNs, and Bi3O4Br/CNNs, the rate constant of MEAs-Bi3O4Br/CNNs was 3.26, 11.16, and 3.17 times higher during the degradation of norfloxacin, respectively. This study provides a new strategy for understanding the mechanism of LSPR and the rational design of plasmonic coupling architectures for enhanced photocatalysis.

Enhancing photocatalytic H2 production and dye degradation: Comparative analysis of gold reduction techniques on Au/TiO2 nanocomposites

This study compares the impact of two reduction techniques, thermal reduction (TR) and photocatalytic reduction (PR), on Au/TiO2 photocatalysts synthesized using the deposition-precipitation with urea method. Characterization methods, including temperature-programmed reduction, UV-Vis diffuse reflectance spectroscopy, electrochemical assessments (open-circuit potential and linear sweep voltammetry), and transmission electron microscopy, were employed. The 2-h. PR treatment yielded a highly effective photocatalyst (0.5Au-PR2), with 93.6% of gold nanoparticles below 4 nm, outperforming the TR counterpart (76.8%). All Au-loaded samples exhibited an absorption band between 400 and 800 nm, indicating the localized surface plasmon resonance (LSPR) effect. Interestingly, the TR catalyst had a broader LSPR band than the PR catalyst. Additionally, the 0.5Au-PR2 sample showed higher photocurrent and superior photocatalytic activity in the degradation of methyl orange and hydrogen production, which is attributed to its smaller particle size (2.9 nm) and weaker metal-support interaction. This smaller particle size emphasizes the crucial role of reduction techniques in tailoring Au/TiO2 photocatalysts for enhanced performance.

Schottky Barrier-Based Built-In Electric Field for Enhanced Tumor Photodynamic Therapy.

Photodynamic therapy's antitumor efficacy is hindered by the inefficient generation of reactive oxygen species (ROS) due to the photogenerated electron-hole pairs recombination of photosensitizers (PS). Therefore, there is an urgent need to develop efficient PSs with enhanced carrier dynamics. Herein, we designed Schottky junctions composed of cobalt tetroxide and palladium nanocubes (Co3O4@Pd) with a built-in electric field as effective PS. The built-in electric field enhanced photogenerated charge separation and migration, resulting in the generation of abundant electron-hole pairs and allowing effective production of ROS. Thanks to the built-in electric field, the photocurrent intensity and carrier lifetime of Co3O4@Pd were approximately 2 and 3 times those of Co3O4, respectively. Besides, the signal intensity of hydroxyl radical and singlet oxygen increased to 253.4% and 135.9%, respectively. Moreover, the localized surface plasmon resonance effect of Pd also enhanced the photothermal conversion efficiency of Co3O4@Pd to 40.50%. In vitro cellular level and in vivo xenograft model evaluations demonstrated that Co3O4@Pd could generate large amounts of ROS, trigger apoptosis, and inhibit tumor growth under near-infrared laser irradiation. Generally, this study reveals the contribution of the built-in electric field to improving photodynamic performance and provides new ideas for designing efficient inorganic PSs.

Synergistic removal of dimethoate through adsorption and photocatalytic oxidation in the presence of FeTiO3@Ag/Ag2O heterojunction

Combining adsorption and photocatalysis as a synergistic technique has become a research trend since adsorption is a prerequisite for photocatalytic surface reactions. In this study, a Z-scheme heterojunction FeTiO3@Ag/Ag2O with local surface plasmon resonance (LSPR) effect was fabricated for the removal of dimethoate from water. Under visible light irradiation, dimethoate could be completely removed within 75 min in the presence of 0.3 g/L FeTiO3@Ag/Ag2O (with Ag2O percentage of 10 wt%). High removal efficiency of dimethoate was mainly attributed to the synergistic effect between the large specific surface area of the catalyst (160.695 m2/g), the formation of heterojunction of FeTiO3 and Ag2O, and the LSPR effect of metal Ag, which reinforced the absorption of visible light and promoted the separation and transfer of the carriers. Radicals of O2− and OH were the main reactive groups triggered the photocatalytic degradation process of dimethoate. Density Functional Theory (DFT) calculations indicate that PS and P–S bonds in the dimethoate molecule were more susceptible to be attacked by reactive groups. The degradation pathways mainly include oxidation of PS bond and cleavage of P–S bond, and the toxicity of most intermediates was reduced when compared with the parent compound. This study exploited the role of adsorption and photocatalysis in the field of pollutant removal, and provides ideas for the preparation of bifunctional photocatalysts.

Boosting the Efficiency of High-Resolution Quantum Dot Light-Emitting Devices Based on Localized Surface Plasmon Resonance.

With pixel miniaturization, the performance of high-resolution quantum dot light-emitting diodes (QLEDs) usually degrades. Considering the dimension of ultrasmall pixels, herein, a barrier architecture based on localized surface plasmon resonance (LSPR) that promotes the radiative recombination of neighboring quantum dots is rationally designed to improve the device performance. Au nanoparticles (NPs) are embedded in an insulating polymer to form a honeycomb-patterned barrier layer via the nanoimprint process. Each pixel fabricated in the void area (average diameter of 1.5 μm) of the barrier layer is surrounded by a number of LSPR-NPs to enhance the luminescence. The resultant green QLEDs with a resolution of 9027 pixels per inch show a maximum external quantum efficiency of 11.1%, a 42.8% enhancement compared to the control device. Additionally, the lifetime of high-resolution QLEDs is obviously improved by the LSPR effect.