Surface Plasmon Resonance Effect Research Articles

TiO2 nanotubes modification by photodeposition with noble metals: Characterization, optimization, photocatalytic activity, and by-products analysis

Self-organized TiO2 nanotubes (TNTs) with 4 µm length were obtained by anodization method and calcined to obtain anatase crystallite phase. The photocatalysts were further decorated with Au, Ag, Pt or Pd nanoparticles (NPs), varying the metal loads (0.50, 0.75, 1, 2 and 5 mol%) by photodeposition. The material characterization confirmed the presence of nanoparticles in the TNTs surface, signs of the localized surface plasmon resonance (LSPR) effect for some samples and a bandgap energy of 3.1–3.2 eV. Photoluminescence measurements also confirmed that most of the samples with metallic nanoparticles had the recombination of photogenerated carriers lowered due to the trapping effect of the deposited metal NPs. The photoactivity was evaluated by phenol degradation using UV-Vis or visible radiation. Under UV-Vis, the best samples (2 and 5 mol% of Au-TNTs and 0.75, 1, and 2 mol% of Pd-TNTs) led to 97% phenol removal in 60 min while pristine TNTs reached 92% removal. Under visible radiation, the pristine and the Au-TNTs led to about 3% removal, with the best sample being 2 mol% Pd-TNTs with 14% removal in 60 min. Similar results were obtained for 1 and 5 mol% Pd-TNTs (12% and 13% of phenol removal, respectively). The by-products analysis suggest different degradation mechanisms and it is observed different kinetic rates for different metal types, metal loads or types of radiation.

Construction of Au quantum dots/nitrogen-defect-enriched graphite carbon nitride heterostructure via photo-deposition towards enhanced nitric oxide photooxidation

The challenge of mitigating pollution stemming from industrial exhaust emissions is a pressing issue in both academia and industry. This study presents the successful synthesis of nitrogen-defect-enriched graphite carbon nitride (g-C3N4) using a two-step calcination technique. Furthermore, a g-C3N4-Au heterostructure was fabricated through the photo-deposited Au quantum dots (QDs). When subjected to visible light irradiation, this heterostructure exhibited robust nitric oxide (NO) photooxidation activity and stability. With its fluffy, porous structure and large surface area, the nitrogen-defect-enriched g-C3N4 provides more active sites for photooxidation processes. The ability of g-C3N4 to absorb visible light is enhanced by the local surface plasmon resonance (LSPR) effect of Au QDs. Additionally, the lifetime of photogenerated charge carriers is extended by the presence of N defects and Au, which effectively prevent photogenerated electron-hole pairs from recombining during the photooxidation process. Moreover, the oxidation pathway of NO was analyzed through In-situ Fourier transform infrared (FT-IR) spectroscopy and Density Functional Theory (DFT) calculation. Computational findings revealed that the introduction of Au QDs decreases the activation energy of the oxidation reaction, thereby facilitating its occurrence while diminishing the formation of intermediate products. As a result, NO is predominantly converted to nitrate (NO3−). This work unveils a novel approach to constructing semiconductor-cocatalyst heterostructures and elucidates their role in NO photooxidation.

Efficient gold recovery from low concentrated Au(S2O3)23− solution through enhanced photocatalysis via photothermal and surface plasmon resonance assistance on MoS2/MXene/Ag

Thiosulfate technique is the most promising method to recover gold from electronic waste (e-waste) and natural ores due to its non-toxicity and high leaching efficiency. However, the bad affinity between Au(S2O3)23− and traditional adsorbents leads to unsatisfied gold recovery performance from leaching solution. In this work, highly efficient recovery of gold from low concentrated Au(S2O3)23− solution was achieved through enhanced photocatalysis process on a novel MoS2/MXene/Ag adsorbent. During recovery procedure, Au(S2O3)23− was in-situ reduced to Au0 by photogenerated electrons and then anchored on MoS2/MXene/Ag. Under Au(S2O3)23− concentration <10 ppm, over 99 % gold recovery performance could achieve within 2 h. Experimental tests have proved that MXene made fully use of near infrared (NIR) light energy to exhibit better photothermal effect, and surface plasmon resonance (SPR) effect of Ag can simultaneously facilitate the separation of electron-hole pairs on MoS2. By means of external temperature input and rapid charge carrier transmission, plenty of electrons were excited from MoS2/MXene/Ag for Au(S2O3)23− recovery. This work paved a pathway for efficient Au(S2O3)23− recovery, which catered to the demand for green production of gold in the future.

Precise regulation of surface plasmonic hotspots in an Au split nanoring coupled system

The signal enhancement in plasmon-enhanced spectroscopy is primarily contributed by hotspots generated through the surface plasmon resonance effect. Precise control of hotspot positions within nanostructures is of great significance in surface-enhanced Raman spectroscopy (SERS) and high spatial resolution imaging. However, predicting the positions of hotspots is challenging due to the small nanogaps and complex plasmonic interactions. In this study, we theoretically investigate the localized surface plasmonic properties of split ring nanostructure. The effects of variations in the inner radius, gap distance and thickness of the split ring on the hotspot distribution at the nanogaps are systematically analyzed using a three-dimensional finite element method. The results demonstrate that precise control over the positions and quantities of hotspots can be achieved by choosing the excitation wavelength and the gap size of the split rings. The calculated maximum Raman enhancement obtained at the hotspots can reach nine orders of magnitude. Our findings not only contribute to a deeper understanding of the SERS enhancement mechanism, but also provide theoretical insights for further development of surface-enhanced fluorescence, plasmonic sensors, and super-resolution imaging in the field of interface spectroscopy.

Interface interaction mediated surface plasmon resonance enhancement promoted visible-light-driven CO2 reduction with water

The conversion of carbon dioxide (CO2) into fuel using solar energy holds significant promise. However, the inefficient use of light and poor production activity have hindered its development. Here, we propose a simple in situ annealing oxidation method by coating a layer of TiO2 outside TiN, a material with a favorable price and localized surface plasmon resonance (LSPR) effect, to create an L-TiNO composite. The yield of CO over L-TiNO (50.8 μmol g−1 h−1) is 56.4 times that over TiO2 (0.9 μmol g−1 h−1) under visible light irradiation in pure aqueous environment, with a selectivity of 95.98%. In-situ Fourier transform infrared (FTIR) measurements reflect the CO2-COOH*-CO conversion route happening on L-TiNO. Characterizations like the Kelvin probe force microscopy (KPFM) technique confirm the generation of built-in electric field, which facilitates efficient carrier separation and migration. Density functional theory (DFT) calculations support that L-TiNO with LSPR effect alters the shape of absorbed CO2 to facilitate generation COOH* via forming hydroxyl end group (Ti-OH) and promotes CO* desorption to CO(g). This work provides valuable insights into the coupling of plasmonic materials with semiconductors to achieve efficient solar energy utilization.

Bi-Doped and Bi Nanoparticles Loaded CeO2 Derived from Ce-MOF for Photocatalytic Degradation of Formaldehyde Gas and Tetracycline Hydrochloride.

Bi/CeO2 (BC-x) photocatalysts are successfully prepared by solvothermal loading Bi nanoparticles and Bi-doped CeO2 derived by Ce-MOF (Ce-BTC). Formaldehyde gas (HCHO) and tetracycline hydrochloride (HTC) are used to evaluate the photocatalytic activity of the synthesized Bi/CeO2. For BC-1000 photocatalyst, the degradation of HTC by 420nm < λ < 780nm light reaches 91.89% for 90min, and HCHO by 350nm < λ < 780nm light reaches 94.66% for 120min. The photocatalytic cycle experiments prove that BC-1000 has good cyclic stability and repeatability. The results of photoluminescence spectra, fluorescence lifetime, photocurrent response, and electrochemical impedance spectroscopy showed that the SPR (Surface Plasmon Resonance) effect of Bi nanoparticles acted as a bridge and promoted electron transfer and enhanced the response-ability of Bi/CeO2 to visible light. Bi-doping produced more oxygen vacancies to provide adsorption sites for adsorbing oxygen and generated more ·O2 - thus promoting photocatalytic reactions. The mechanism of photocatalytic degradation is analyzed in detail utilizing active free radical capture experiments and electron paramagnetic resonance (EPR) characterization. The experimental results indicate that ·O2 - and h+ active free radicals significantly promote the degradation of pollutants.

Ultrasensitive dual-mode detection of amyloid β oligomer via Au NRs modulated photoelectrochemical/electrochemiluminescent response from HOFs/g-C3N4

In this work, a heterojunction composite of HOFs/g-C3N4 was synthesized using solution-plasticized self-assembly of g-C3N4 nanosheet on hydrogen-bonded organic frameworks (HOFs). HOFs/g-C3N4 was then used as a substrate material to construct a novel photoelectrochemical/electrochemiluminescent (PEC/ECL) biosensor for the detection of amyloid β oligomer (Aβo). HOFs/g-C3N4 composites were first drop-coated on the electrode surface. Subsequently, the Aβ aptamer was modified on the electrode surface via amide bonding. The target Aβo and the gold nanorods (Au NRs)-labeled Aβ recognition peptide (Au NRs-KLVFF) were simultaneously dropped onto the electrode surface, thus a “sandwich” dual-mode biosensor was constructed. In the PEC detection of the Aβo, the surface plasmon resonance effect of Au NRs enhanced the visible absorption of HOF/g-C3N4, and the sensor exhibited a "signal-on" photocurrent signal. Meanwhile, the ECL emission spectrum of HOF/g-C3N4 in ECL mode overlaps with the ultraviolet-visible (UV) absorption of Au NRs, and the sensor signal showed a “signal-off” ECL response. Under the optimal conditions experiments, the constructed dual-mode biosensor showed a wide detection range and low detection limit for Aβo. The proposed dual-mode detection method has a detection range of 10 fM to 10 nM with a detection limit of 5.97 fM for PEC detection and a detection range of 0.1 pM to 1.0 μM with a detection limit of 0.051 pM for ECL detection respectively. Additionally, the detection method achieved satisfactory results in the analysis of real samples. Dual-mode sensing platform provides a new strategy for HOFs application in PEC/ECL assay and sensitive detection of AβO.

SERS monitoring of methylene blue degradation by Au-Ag@Cu2O-rGO nanocomposite

A combination of multiple materials effectively improves and enhances the performance of the materials. Thus, a gold-silver@cuprous oxide (Au-Ag@Cu2O)-reduced graphene oxide (rGO) structure was designed and fabricated. We decorated the Au nanoparticles (NPs) on the Ag@Cu2O-rGO composite surface by a redox reaction to form a Au-Ag@Cu2O-rGO structure with two noble metals attached to a Cu2O semiconductor. A comparable Au-Ag@Cu2O structure was also fabricated. After decorating Au NPs into the Ag@Cu2O-rGO composite, the Au-Ag@Cu2O composite structure was loosened, and the surface and interior of the Cu2O shell were decorated with Au and Ag NPs. Moreover, the addition of Au NPs resulted in a proper surface plasmon resonance effect and a significant broadening of the absorption range. The loose structure increased the adsorption of the probe molecules, which increased the surface-enhanced Raman scattering (SERS) intensity. In addition, the fabricated Au-Ag@Cu2O-rGO exhibited excellent catalytic reduction of methylene blue (MB) with sodium borohydride (NaBH4). Therefore, the SERS-based monitoring of the MB degradation was obviously improved.

Promoting the optoelectronic and nonlinear optics properties of MoS2 nanosheets via metal Al anchoring

Molybdenum disulfide (MoS2) has attracted much attention in the field of optoelectronic materials due to its stability and adjustable bandgap structure. However, improving the optoelectronic properties of MoS2 is still a challenging research. Herein, Al doped MoS2 (AMS) films were prepared by a simple single-step magnetron sputtering method. The bonding modes of Al implantation and auxiliary MoS2 were investigated by adjusting metal Al anchoring. The successful synthesis of AMS films was confirmed by the analysis of X-ray diffraction and X-ray photoelectron spectroscopy measurements to investigate the diffraction peaks of Al and Al2S3 and the valence electron structures of Al3+. Compared to MoS2, the A1g Raman peaks of AMS films are slightly blue-shifted, and the peak positions of both Mo3d and S2p are slightly shifted towards higher binding energies. This is attributed to the surface plasmon resonance effect produced by Al doping resulting in a large amount of electron transfer to the conduction band (CB) of MoS2. In addition, the density functional theory calculations reveal that Al doping of MoS2 results in a higher concentration of electrons in CB of MoS2, the band gap of MoS2 can be adjusted by changing the doping concentration of Al. The Z-scan results illustrated that MoS2 was converted from saturable absorption to reverse saturable absorption (RSA) by adjusting the sputtering power of Al. This is attributed to the fact that Al doping increases the electron concentration in the CB of MoS2, which promotes the RSA of the excited states and doping energy levels of AMS films. The values of the nonlinear absorption coefficients of AMS films are 2–5 times higher than those of MoS2, which significantly improves the nonlinear absorption performance of MoS2. The carrier relaxation process and kinetic mechanism of AMS films were investigated by transient absorption spectroscopy, moderate doping of Al can effectively improve the carrier lifetime. This implies that AMS films have good optoelectronic properties and have a wide application potential in optoelectronic devices.

Dealloying-Derived Self-Supporting Nanoporous Zinc Film with Optimized Macro/Microstructure for High-Performance Solar Steam Generation.

Solar steam generation (SSG) is a promising technology for the production of freshwater that can help alleviate global water scarcity. Nanostructured metals, known for their localized surface plasmon resonance effect, have generated significant interest, but low-cost metal films with excellent water evaporation properties are challenging. In this work, we present a one-step dealloying route for fabricating self-supporting black nanoporous zinc (NP-Zn) films with a bicontinuous ligament/channel structure, using Al-Zn solid solution alloys as the precursors. The influence of alloy composition on the formation and macro/microstructure of NP-Zn was investigated, and an optimal Al98Zn2 was selected. Additionally, in situ and ex situ characterizations were conducted to unveil the dealloying mechanism of Al98Zn2 and phase/microstructure evolution of NP-Zn during dealloying, including the phase transition of Al(Zn) → Zn, significant volume shrinkage (89.8%), and the development of high porosity (81.3%). The nanoscale ligament/channel structure and high porosity endow the NP-Zn films with good broadband absorption and superior hydrophilicity and, more importantly, give them excellent SSG performance. The NP-Zn2 film displays high evaporation efficiency, superior stability, and good seawater desalination performance. The efficient SSG performance, material abundance, and low cost suggest that NP-Zn films have promising applications in metal-based photothermal materials for SSG.

Construction of flexible BiOBr/W18O49/polyacrylonitrile discrete heterojunction nanofibers as a dual-functional photocatalyst for simultaneous hydrogen evolution and organic pollutant degradation

Dual-functional photocatalysis has attracted increasing attention due to its ability to achieve efficient synergistic hydrogen (H2) evolution and pollutant removal. Energy band structure engineering and surface morphology modification of photocatalysts is a useful strategy to improve the activity of photocatalysis. This paper uses a combination of electrospinning technology and hydrothermal method to prepare flexible BiOBr/W18O49/PAN discrete heterojunction flexible nanofibers (NFs) with staggered energy bands and spatially separated redox surfaces. The BiOBr/W18O49 heterojunction can improve carrier separation and migration, as evidenced by the photoluminescence and photoelectrochemical experiments. The localized surface plasmon resonance (LSPR) effect of W18O49 can achieve injection of “hot electrons” and lead to expanding the light absorption range according to the UV–visible-near infrared diffuse reflection spectra results. The discrete structure of BiOBr/W18O49/PAN NFs can provide spatially separated active sites for simultaneous photocatalytic redox reaction. As expected, the BiOBr/W18O49/PAN discrete heterojunction NFs greatly enhance the photocatalytic activity in simultaneous dual-functional reaction for H2 evolution and RhB degradation. The highest simultaneous H2 evolution rate and RhB degradation rate of BiOBr/W18O49/PAN NFs are 31.7 times and 34.1 times of BiOBr/PAN, respectively. The design and construction of this flexible discrete heterojunction NFs structures can provide novel ideas and directions for simultaneous dual-functional photocatalysts.

Nanopore arrays with TMOKE-enhanced high performance sensing

Magneto-plasmon sensing structure based on surface plasmon resonance (SPR) and magneto-optical (MO) effect has become a hot research topic in recent years. In this work, we propose a magneto-plasmon crystal consisting of an Au/Co double-layer nanoporous structure with optically thick Au film as a substrate. Due to the excitation of high-quality SPR, a Fano-like transverse magneto-optical Kerr (TMOKE) spectrum with subnanometer bandwidth is realized. A sensitivity of up to 677 nm RIU−1 is detected under subtle refractive index changes in air, and all the calculated figure of merits (FOM) are higher than 104 RIU−1. In addition, in order to highlight the superiority of the sensing performance of the MO plasmon (MOSPR) sensor, we compare the MOSPR sensor with the SPR sensor and calculate their FOM in different refractive index environments. The results show that the FOM of the MOSPR sensor is two orders of magnitude higher than that of the SPR sensor, which proves that the performance of the MOSPR sensor is significantly better than that of the SPR sensor and provides a theoretical basis for biosensing and gas detection based on magneto plasmon.

Experimental study on ultra-high sensitivity gold-based SPR sensor for refractive index and temperature measurement

We have experimentally demonstrated an ultra-high sensitivity gold-based fiber refractive index (RI) sensor whose main structure is composed of multimode fiber (MMF) and photonic crystal fiber (PCF). The gold film is deposited on V-shaped PCF by magnetron sputtering, and sensing experiments are performed based on the principle of surface plasmon resonance (SPR). Numerical simulation results indicate that the cladding mode of the V-shaped PCF is more capable of stimulating the SPR effect than the core mode. The experimental results show that the RI measurement range of the sensor is 1.333–1.421, with a maximum sensitivity of 10015 nm/RIU. In addition to RI sensing, sensing probes can be coated with polydimethylsiloxane (PDMS) on a gold film for temperature sensing. For temperature detection, the range is from 10 to 100 °C and the maximum sensitivity is 3.5 nm/℃. Besides high sensitivity in RI measurement, the proposed sensor also has good sensing performance in temperature sensing. With the advantages of high sensitivity, good stability, and easy preparation, this sensor has become an important reference in the field of high-performance sensing.

Enhanced photocatalytic H2 evolution over conjugated polymer/Au@TiO2 ternary heterojunction under visible light: Enriched photons input from polymers

Exploring efficient and stable TiO2-based photocatalysts for visible-light H2 evolution remains a great challenge. Here, a novel ternary heterojunction (THSO/Au@TiO2) was successfully synthesized by a facile in-situ polymerization strategy, which showed highly enhanced photocatalytic activity towards H2 evolution under visible light. The optimized THSO/Au@TiO2-26 exhibited an excellent photocatalytic performance to H2 evolution (7504 μmol/g/h), which was 16.31, 416.89 and 1.81 times higher than that of THSO, TiO2 and THSO/TiO2 photocatalysts, respectively. This excellent performance should be attributed to the excellent visible light absorption ability of the polymer THSO, and the local surface plasmonic resonance effect of Au nanoparticles (Au NPs), promoting separation and transfer of photo-generated charge carriers. This work presents new insights for the design of efficient and rational TiO2-based photocatalytic systems to enhance photocatalytic performance towards H2 evolution under visible light.

Enhanced photoluminescence in graphene wrapped hydrophobic zinc oxide

This article reports the synthesis of zinc oxide (ZnO) rod like structures over different substrates. The developed ZnO was further wrapped with graphene sheet and thus the hybrid was formed.The samples were characterized by X-ray diffraction, electron microscopy, UV–Vis and Fourier transformed infrared spectroscopy.After graphene wrapping the surface energy of ZnO reduced resulting enhanced hydrophobicity. Also, graphene inclusion enhances the photoluminescence intensity of the underlying ZnO for both band edge and defect induced transition.This enhancement in the PL intensity may be assigned to the supply of electron from the graphene to ZnO or surface plasmon resonance effect.

Sodium-based no-core fiber surface plasmon resonance sensor with high sensitivity and narrow FWHM

Since fiber-optic sensors using noble metal-excited surface plasmon resonance (SPR) effects have encountered bottlenecks in improving performance, we propose a fiber-optic sensor using sodium in combination with a no-core fiber (NCF) to measure both refractive index (RI) and temperature. We deposited sodium thin films on the surface of NCF optical fibers and protected them with polymethyl methacrylate (PMMA) or polydimethylsiloxane (PDMS) for RI sensing or temperature sensing. We performed computational simulations and performance analyses of the sensors using the finite element method, and the results show that the sodium-based SPR sensors have higher sensitivity, wider detection range, and narrower full width at half-maximum (FWHM) than the noble metal SPR sensors. SPR sensors with different sodium film thicknesses have different sensing characteristics, so we can get optical fiber sensors with more flexible transmission characteristics, which helps us arrange sensors more conveniently in practical applications. The simulation and numerical results show that when the sensor is used to measure RI, the average sensitivity of the sensor can reach 7977 nm RIU−1, the maximum sensitivity can reach 23100 nm RIU−1, the narrowest FWHM is 14.23 nm, and the maximum figure of merit (FOM) is 719.42 RIU−1 under different thicknesses of sodium film. The corresponding RI ranges from 1.32 to 1.41. When the temperature measurement range is 0 °C ∼ 100 °C, the average sensitivity can reach 7.86 nm °C−1, the maximum temperature sensitivity can reach 21.1 nm °C−1, and the narrowest FWHM is 17.84 nm. In summary, the proposed sodium-based SPR sensor has flexible and high-performance sensing characteristics, and our research work provides more powerful theoretical support for the application of sodium-based plasma devices.

Investigation of a Pyramid-like Optical Absorber with High Absorptivity in the Range of Ultraviolet A to Middle Infrared

In this study, a simple pyramid-like ultra-wideband absorber was designed to explore high absorptivity across a wide bandwidth. The absorber consisted of eight layers organized into four groups, and each group comprised a metal layer followed by an oxide layer, both of which were square with equal side lengths. Specifically, the chosen oxides, arranged from bottom to top, included SiO2 (t7 layer), Al2O3 (t5 layer), SiO2 (t3 layer), and Al2O3 (t1 layer). In the initial design phase, the thickness of the t8 Ti layer was set to 50 nm and assigned initial values to the thicknesses of the t7-t1 layers, and the widths of the four groups w4, w3, w2, and w1, decreased successively from bottom to top, creating a structure reminiscent of a pyramid. Comsol (version 6.0) was utilized to simulate and systematically vary one parameter at a time, ranging from the thicknesses of the t7-t1 layers to the widths of w4-w1, in order to identify the most suitable structural parameters. Our analyses demonstrated that multimode resonance arose due to the emergence of absorption peaks at lower wavelengths between larger and smaller areas. Additionally, surface plasmon resonance and interference effects between various layers and materials were attributed to the alternating arrangement of metal and oxide layers. The enhancements in the electric field observed at different resonance peak wavelengths illustrated the Fabry–Perot cavity effect, while the impedance matching effect was observed through variations in the real and imaginary parts of the optical impedance with respect to the wave vector. After simulating using these optimally found thicknesses and widths, the aforementioned effects manifested in the pyramid-like ultra-wideband absorber we designed, with its absorptivity surpassing 0.900 across the spectrum from ultraviolet A (335 nm) to middle infrared (4865 nm).

Built-in electric field intensified by SPR effect to drive charge separation over Ag-AgI/Sb2S3 heterojunction for high-efficiency photocatalytic metronidazole mineralization

The photocatalytic activity of semiconductor is extremely limited due to the rapid recombination of photo-generated carriers and low utilization of solar energy. Herein, a novel Ag-AgI/Sb2S3 (A-S) heterojunction with superior photocatalytic activity was synthesized, in which the optimal Ag-AgI/Sb2S3 heterojunction exhibited 31 times photocatalytic activity of metronidazole removal than that of than that of Sb2S3. The excellent performance of the prepared photocatalysts could be attributed to the synergy of surface plasmon resonance effect by in situ-generated Ag nanoparticles and the built-in electric field of heterostructure, which would broaden the response range of solar light and accelerate the transfer of photogenerated carriers. Besides, characterization and theoretical calculations confirm Ag atoms acquire abundant electrons from Sb atoms of Sb2S3, allowing Ag+ to reduce to Ag0. Meanwhile, a portion of the Ag0 plasma-induced hot electrons reduce O2 to ·O2–, while the remaining portion flows to AgI and circulates in AgI and Ag0 to form a closed loop, thus eliminating the photo-corrosion of AgI. The stability of A-S photocatalyst was also confirmed by five cycle-tests. Furthermore, a reasonable photocatalytic mechanism was proposed by analyzing the intermediates of metronidazole. This work has implications for designing efficient photocatalysts using high-performance materials based on Ag nanoparticles.

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 = 23,400 cd/m2, EQE = 1.55) are obviously boosted as compared to the control device (Von = 2.9 V, L = 19,780 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.

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.