Strong Localized Surface Plasmon Resonance Research Articles

Gold Nanoparticles: Multifunctional Properties, Synthesis, and Future Prospects

Gold nanoparticles (NPs) are among the most commonly employed metal NPs in biological applications, with distinctive physicochemical features. Their extraordinary optical properties, stemming from strong localized surface plasmon resonance (LSPR), contribute to the development of novel approaches in the areas of bioimaging, biosensing, and cancer research, especially for photothermal and photodynamic therapy. The ease of functionalization with various ligands provides a novel approach to the precise delivery of these molecules to targeted areas. Gold NPs’ ability to transfer heat and electricity positions them as valuable materials for advancing thermal management and electronic systems. Moreover, their inherent characteristics, such as inertness, give rise to the synthesis of novel antibacterial and antioxidant agents as they provide a biocompatible and low-toxicity approach. Chemical and physical synthesis methods are utilized to produce gold NPs. The pursuit of more ecologically sustainable and economically viable large-scale technologies, such as environmentally benign biological processes referred to as green/biological synthesis, has garnered increasing interest among global researchers. Green synthesis methods are more favorable than other synthesis techniques as they minimize the necessity for hazardous chemicals in the reduction process due to their simplicity, cost-effectiveness, energy efficiency, and biocompatibility. This article discusses the importance of gold NPs, their optical, conductivity, antibacterial, antioxidant, and anticancer properties, synthesis methods, contemporary uses, and biosafety, emphasizing the need to understand toxicology principles and green commercialization strategies.

Plasmonic semi shells derived from simultaneous in situ gold growth and anisotropic acid etching of ZIF-8 for photothermal ablation of metastatic breast tumor

Open nanoshells such as nanobowls or nanocups collectively described as ‘semi shells’ have unique plasmonic properties due to their lack of symmetry. So far, their fabrication was based on multistep and laborious methods such as solid state sputter coating or selective deposition/etching using sacrificial templates. In this work, we report a rapid one step colloidal synthetic protocol for PEGylated semi-shell (SS) fabrication by simultaneous facet specific anisotropic chemical etching of rhombic dodecahedral ZIF-8 and heterogenous nucleation & growth of gold. The SS possesses a strong localized surface plasmon resonance in the near-infrared region, which is retained after surface passivation with polyethylene glycol and subsequent cryopreservation for extended shelf-life. Freshly reconstituted PEGylated SS was found to be safe & non-toxic in healthy C57BL/6 mice post intravenous administration. The PEGylated SS displayed significant photothermal efficiency of ~37% with 808 nm laser irradiation. Preclinical assessment of intra-tumoral photothermal efficacy indicated complete remission of primary breast tumor mass with insignificant metastasis to vital organs in 4T1 FL2 tumor bearing CD1 nude mice. Further, PEGylated SS mediated photothermal therapy also yielded morbidity free survivael of 75% for up to 90 days, indicating their potential to significantly improve outcomes in advanced breast tumors.

Highly sensitive, reproducible, and stable core–shell MoN SERS substrate synthesized via sacrificial template method

Molybdenum nitride is a promising candidate for surface-enhanced Raman scattering (SERS) substrates due to its high conductivity, surface plasmon resonance, and chemical stability. Core-shell structures possess unique physical and chemical properties, such as high-volume ratio, low density, short diffusion length, and high load-bearing capacity, making them favorable for SERS applications. In this research, core–shell MoO3 is first synthesized as a precursor oxide using a sacrificial template method, and core–shell MoN microspheres are successfully prepared via subsequent nitriding. As a representative transition metal nitride, the obtained core–shell MoN nanospheres show strong localized surface plasmon resonance and SERS effects. Using these MoN microspheres as Raman substrates allows a range of highly targeted compounds to be accurately detected, and the detection limits for this non-precious-metal substrate morphology are exceptionally high, reaching 10−10 M. In addition, MoN nanospheres exhibit excellent resistance to acid–base corrosion, oxidation, and radiation, thus rendering them suitable for use as substrates in harsh environments.

Aggregated gold nanoparticles rich in electromagnetic field “hotspots” for surface enhanced Raman scattering

A simple method for one-step synthesis of aggregated gold nanoparticles (a-AuNPs) using single-layer carbon dots (s-CDs) as the capping agents has been proposed. The obtained a-AuNPs are mainly composed of several spherical AuNPs of 20–25 nm sized, which aggregate to form nanogaps of ∼1 nm. Furthermore, the obtained a-AuNPs produce a strong localized surface plasmon resonance (LSPR) absorption band centered at around 640 nm, which is quite close to the wavelength of the commonly used 633 nm laser in surface enhanced Raman scattering (SERS). Thus, under the irradiation of 633 nm laser, a lot of electromagnetic field “hot spots” are formed at around the nanogaps, and strong SERS activity is achieved. The obtained a-AuNPs are dropped on tin-foil wafers to fabricate SERS substrates, which show the advantages of high sensitivity, fast response, good repeatability and satisfactory stability. On the basis, a sensitive SERS sensor is developed to detect malachite green in aquaculture water, with a low detection limit of 1 × 10−9 mol/L.

Titanium boride nanosheets with photo-enhanced sonodynamic efficiency for glioblastoma treatment

Sonodynamic therapy (SDT) has garnered significant attention in cancer treatment, however, the low-yield reactive oxygen species (ROS) generation from sonosensitizers remains a major challenge. In this study, titanium boride nanosheets (TiB2 NSs) with photo-enhanced sonodynamic efficiency was fabricated for SDT of glioblastoma (GBM). Compared with commonly-used TiO2 nanoparticles, the obtained TiB2 NSs exhibited much higher ROS generation efficiency under ultrasound (US) irradiation due to their narrower band gap (2.50 eV). Importantly, TiB2 NSs displayed strong localized surface plasmon resonance (LSPR) effect in the second near-infrared (NIR II) window, which facilitated charge transfer rate and improved the separation efficiency of US-triggered electron–hole pairs, leading to photo-enhanced ROS generation efficiency. Furthermore, TiB2 NSs were encapsulated with macrophage cell membranes (CM) and then modified with RGD peptide to construct biomimetic nanoagents (TiB2@CM-RGD) for efficient blood-brain barrier (BBB) penetrating and GBM targeting. After intravenous injection into the tumor-bearing mouse, TiB2@CM-RGD can efficiently cross BBB and accumulate in the tumor sites. The tumor growth was significantly inhibited under simultaneous NIR II laser and US irradiation without causing appreciable long-term toxicity. Our work highlighted a new type of multifunctional titanium-based sonosensitizer with photo-enhanced sonodynamic efficiency for GBM treatment. Statement of significanceTitanium boride nanosheets (TiB2 NSs) with photo-enhanced sonodynamic efficiency was fabricated for SDT of glioblastoma (GBM). The obtained TiB2 NSs displayed strong localized surface plasmon resonance (LSPR) effect in the second near-infrared (NIR II) window, which facilitated charge transfer rate and improved the separation efficiency of US-triggered electron-hole pairs, leading to photo-enhanced ROS generation efficiency. Furthermore, TiB2 NSs were encapsulated with macrophage cell membranes (CM) and then modified with RGD peptide to construct biomimetic nanoagents (TiB2@CM-RGD) for efficient blood-brain barrier (BBB) penetrating and GBM targeting. After intravenous injection into the tumor-bearing mouse, TiB2@CM-RGD can efficiently cross BBB and accumulate in the tumor sites. The tumor growth was significantly inhibited under simultaneous NIR II laser and US irradiation without causing appreciable long-term toxicity.

Selenium-Doped Seeded Growth of Truncated Octahedral Gold Nanocrystals with Surface Concavities for Surface-Enhanced Raman Spectroscopy.

Concave nanocrystals stand out as a testament to the importance of the nanoscale morphology in dictating the functional properties of materials. In this report, we introduce a facile synthesis method for producing gold (Au) nanocrystals with a truncated octahedral morphology that features surface concavities (Au CNTOs). The incorporation of selenium (Se) doping into the truncated octahedral Au seeds was essential for their enlargement and the formation of concave structures. By simply adjusting the quantity of seeds, we could control the size of the nanocrystals while maintaining their distinctive morphology and surface concavity. The formation mechanism suggests that Se doping likely passivates the side faces, thereby slowing growth and promoting atomic deposition at the edges and corners. The resulting Se-doped Au CNTOs exhibited strong localized surface plasmon resonance (LSPR) absorptions in the visible spectrum and the SERS performance of their assemblies was demonstrated through crystal violet detection, reaching enhancement factors around 105. This study presents an innovative approach to synthesizing concave Au nanocrystals through the incorporation of selenium during a seeded growth process, offering insights into the strategic design of plasmonic nanostructures.

Simultaneous noninvasive ultrasensitive detection of prostate specific antigen and lncRNA PCA3 using multiplexed dual optical microfibers with strong plasmonic nanointerfaces

Low accuracy of diagnosing prostate cancer (PCa) was easily caused by only assaying single prostate specific antigen (PSA) biomarker. Although conventional reported methods for simultaneous detection of two specific PCa biomarkers could improve the diagnostic efficiency and accuracy, low detection sensitivity restrained their use in extreme early-stage PCa clinical assay applications. In order to overcome above drawbacks, this paper herein proposed a multiplexed dual optical microfibers separately functionalized with gold nanorods (GNRs) and Au nanobipyramids (Au NBPs) nanointerfaces with strong localized surface plasmon resonance (LSPR) effects. The sensors could simultaneously detect PSA protein biomarker and long noncoding RNA prostate cancer antigen 3 (lncRNA PCA3) with ultrahigh sensitivity and remarkable specificity. Consequently, the proposed dual optical microfibers multiplexed biosensors could detect the PSA protein and lncRNA PCA3 with ultra-low limit-of-detections (LODs) of 3.97 × 10−15 mol/L and 1.56 × 10−14 mol/L in pure phosphorus buffer solution (PBS), respectively, in which the obtained LODs were three orders of magnitude lower than existed state-of-the-art PCa assay technologies. Additionally, the sensors could discriminate target components from complicated physiological environment, that showing noticeable biosensing specificity of the sensors. With good performances of the sensors, they could successfully assay PSA and lncRNA PCA3 in undiluted human serum and urine simultaneously, respectively. Consequently, our proposed multiplexed sensors could real-time high-sensitivity simultaneously detect complicated human samples, that providing a novel valuable approach for the high-accurate diagnosis of early-stage PCa individuals.

Metallic Degenerately Doped Free-Electron-Confined Plasmonic Nanocrystal and Infrared Extinction Response

In this paper, synthetically scaled-up degenerately n-type doped indium tin oxide (Sn:In2O3) nanocrystals are described as highly transparent conductive materials possessing both optoelectronic and crystalline properties. With tin dopants serving as n-type semiconductor materials, they can generate free-electron carriers. These free electrons, vibrating in resonance with infrared radiation, induce strong localized surface plasmon resonance (LSPR), resulting in efficient infrared absorption. To commercialize products featuring Sn:In2O3 with localized surface plasmon resonance, a scaled-up synthetic process is essential. To reduce the cost of raw materials during synthesis, we aim to proceed with synthesis in a large reactor using industrial raw materials. Sn:In2O3 can be formulated into ink dispersed in solvents. Infrared-absorbing ink formulations can capitalize on their infrared absorption properties to render opaque in the infrared spectrum while remaining transparent in the visible light spectrum. The ink can serve as a security ink material visible only through infrared cameras and as a paint absorbing infrared light. We verified the transparency and infrared absorption properties of the ink produced in this study, demonstrating consistent characteristics in scaled-up synthesis. Due to potential applications requiring infrared absorption properties, it holds significant promise as a robust platform material in various fields.

Mesoporous platinum@copper selenide-based NIR-II photothermal agents with photothermal conversion efficiency over 80% for photoacoustic imaging and targeted cancer therapy

Elevating photothermal conversion efficiency (PCE) is the key to enhance curative efficacy during photothermal therapy. Nevertheless, current functionalized or synthetic methods for preparing photothermal agents with high PCE are too complicated, greatly hindering the development of photothermal therapy. In this study, we developed a tumor-targeting flower-like nanocomposite termed mesoporous platinum nanoparticles@Cu2-xSe-AS1411 (MPNPs@Cu2-xSe-AS1411, denoted as MPCSA) with remarkable PCE for high-resolution photoacoustic (PA) imaging guided photothermal/chemodynamic therapy for tumor ablation. We discovered that MPNPs served as carriers for delivering PA contrast agents. Cu2-xSe nanosheets emerged as promising near-infrared-II (NIR-II) PA imaging and photothermal/chemodynamic therapy agents owing to their strong localized surface plasmon resonance property in the NIR-II region. The amine-modified AS1411 aptamer, which is connected to the surface of the flower-like MPNPs@Cu2-xSe can target the nucleolar protein on the surface of 4T1 cells, achieving the accumulation of MPCSA at the tumor site in mice. Notably, these MPCSA nano-flowers exhibited an excellent PCE up to 82.33 % under 1064 nm laser irradiation, resulting in highly efficient cancer cell ablation and greatly hindering in vivo tumor growth. This study has paved the way for imaging-guided accurate cancer diagnosis and targeted cancer therapy.

Photothermal properties of Cu@polycarbonate composites with strong localized surface plasmon resonances

Photothermal properties of Cu@polycarbonate composites with strong localized surface plasmon resonances

Antimony-Doped Wide Bandgap Molybdenum Trioxide with Enhanced Localized Surface Plasmon Resonance for Nitrogen Photofixation.

Plasmonic metal oxides are promising photocatalysts for the artificial photosynthesis of green ammonia due to localized surface plasmon resonance (LSPR) enhanced photoconversion and rich surface oxygen vacancies improved chemisorption and activation of dinitrogen molecules. However, these oxygen vacancies are unstable during the photocatalytic process and could be oxidized by photogenerated holes, leading to the vanishing of the LSPR. Here, we fabricated antimony-doped molybdenum trioxide nanosheets with stable plasmonic absorption extending into the near-infrared (NIR) range, even after harsh treatment in oxidative atmospheric conditions at high temperatures. For undoped plasmonic MoO3-x nanosheets, the LSPR originates from the abundant oxygen vacancies that vanish after heat treatment at high temperatures in air, leading to the disappearance of the LSPR absorption. Sb doping does not significantly increase the concentration of oxygen vacancies while donating more free electrons because Sb can keep a lower oxidation state. Heat treatment diminished the oxygen vacancies while not affecting the low oxidation state of Sb. As a result, heat-treated Sb-doped MoO3-x nanosheets still show strong LSPR absorption in the NIR range. Both experimental results and theoretical calculations demonstrated that add-on states close to the Fermi level are formed due to the Sb doping and high concentration of oxygen vacancies. The prepared samples were used for photocatalytic nitrogen reduction and showed an LSPR-dependent photocatalytic performance. The present work has provided an effective strategy to stabilize the LSPR of plasmonic semiconductor photocatalysts.

Facile synthesis of Ag/AgCl/PAF-54 heterojunction photocatalysts for TC degradation

Photocatalysis plays an increasingly important role in the field of water treatment. Among the catalysts, Ag nanoparticles (NPs), a type of noble metal NP, show extraordinary potential for photocatalysis. Nevertheless, the aggregation caused by high surface energy limits their applications. The simple synthesis of Ag NPs with uniform size remains a challenge. In this work, a nitrogen-rich porous organic polymer (POP) with reduction ability, porous aromatic framework (PAF)-54, was chosen as the carrier for the in-situ synthesis of Ag NPs. By virtue of the reducing framework of PAF-54 and the formation of the AgCl/PAF-54 heterojunction, the in-situ reduction of Ag(I) was realized, and thus Ag NPs with the particle size of 20-25 nm were uniformly distributed on PAF-54, which exhibit a strong localized surface plasmon resonance (LSPR) effect. Furthermore, the Ag/AgCl/PAF-54 heterojunction effectively suppresses the recombination of photogenerated electrons and holes, leading to the enhanced photocatalytic ability of the composite material. Even with a small catalyst dosage, rapid tetracycline (TC) degradation can be achieved, and the degradation rate of TC reached 94.8% in 30 min. This study offers a facilitated approach for fabricating Ag-based POP composites with superior photocatalytic properties.

Infrared light driven overall water vapor splitting on a plasmonic semiconductor p-n heterojunction photocatalyst

Photocatalytic overall water splitting (OWS) has yet to be realized on plasmonic semiconductor photocatalysts. In this work, we reported a plasmonic heterojunction of p-Cu1.81S/n-CdS with homogeneously distributed p-type and n-type domains in a single nanoparticle. The plasmonic heterojunction displays a strong localized surface plasmon resonance (LSPR) absorption peak at 1480 nm and can drive the OWS into hydrogen and oxygen under infrared light (IR) irradiation. The IR light-induced hot electrons and holes in Cu1.81S nanodisks alone can split water vapor into hydrogen and oxygen, but with poor efficiency. Surprisingly, the plasmonic p-Cu1.81S/n-CdS heterojunction shows significantly improved IR light-driven OWS performance. Under the irradiation of IR light (λ > 800 nm), the hydrogen and oxygen production rates were 0.73 mmol gcat−1 h−1 and 0.33 mmol gcat−1 h−1, respectively. The heterojunction photocatalyst delivered a solar-to-hydrogen conversion efficiency (STH) of 0.02 % under AM 1.5G irradiation. The present study has demonstrated that plasmonic semiconductors are promising photocatalysts for harvesting IR light for green hydrogen generation.

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.

High-sensitivity refractive index sensor based on strong localized surface plasmon resonance.

This study proposes two types of composite structures based on gold nano circular and nano square rings on a gold thin film for plasmonic refractive index sensing. The finite-difference time-domain method was used for simulation and analysis. The nano square ring composite structure showed superior performance, with five surface plasmon resonance modes, and a peak sensitivity and figure of merit in a liquid environment of 1600nm/RIU and 86R I U -1, respectively. The sensing performances of localized surface plasmon resonance modes of both structures are superior to those of the propagating surface plasmon resonance modes. The proposed composite structures can provide a reference for refractive index sensing and have broad application prospects in bio-chemistry.

Scalable synthesis of Au@CeO2 nanozyme for development of colorimetric lateral flow immunochromatographic assay to sensitively detect heart-type fatty acid binding protein

Nanozymes with core@shell nanostructure are considered promising biolabeling materials for their multifunctional properties. In this work, a simple one-pot strategy has been proposed for scalable synthesis of gold@cerium dioxide core@shell nanoparticles (Au@CeO2 NPs) with strong localized surface plasmon resonance (LSPR) absorption and high peroxidase-like catalytic activity by redox reactions of Ce3+ ions and AuCl4− ions in diluted ammonia solution under room temperature. A colorimetric lateral flow immunochromatographic assay (LFIA) has been successfully fabricated for sensitive detection of heart-type fatty acid binding protein (H-FABP, an early cardiac biomarker) by using the Au@CeO2 NPs as reporters. The as-developed LFIA with Au@CeO2 NP reporter (termed as Au@CeO2-LFIA) exhibits a dynamic range of nearly two orders of magnitude, and a limit of detection (LOD) as low as 0.35 ng mL−1 H-FABP with nanozyme-triggered 3,3′,5,5′-tetramethylbenzidine (TMB) colorimetric amplification. Furthermore, the practicality of Au@CeO2-LFIA has been demonstrated by profiling the concentrations of H-FABP in 156 blood samples of acute myocardial infarction (AMI) patients, and satisfactory results are obtained.

High enhancement, low cost, large area surface enhanced Raman scattering substrates all by atomic layer deposition on porous filter paper

We successfully developed an atomic layer deposition (ALD) method for making Ag noble nanoparticles on cheap, commercial filter paper consisting of three-dimensional porous glass fibers and investigated the evolution of Ag nanostructures with some key process parameters. By tuning Ag particle sizes and controlling the cycle numbers of ALD deposited Ag films, we were able to obtain high-density isolated Ag nanoparticles with average sizes in 3–9 nm without the formation of agglomerates and continuous Ag films. We proved the presence of strong localized surface plasmon resonance peaks near a target wavelength of 632 nm. We further proved the presence of surface enhanced Raman scattering (SERS) signals on the Ag coated filter paper substrates using pyridine as the test analyte. Our results demonstrate that ALD is a very promising technique for a rational design of SERS substrates and, thus, has great potential for the fabrication of large-area, low-cost SERS substrates for future commercial applications, as compared to other existing techniques.

Recent advance on fiber optic SPR/LSPR-based ultra-sensitive biosensors using novel structures and emerging signal amplification strategies

Biomarkers with ultralow concentration in the actual samples play a vital role in the clinical disease diagnosis, infectious disease screening, food security, and environmental monitoring. Fiber optic (FO)-based surface plasmon resonance (SPR) and localized surface plasmon resonance (LSPR) biosensors attract immense attention for in situ, and rapid detection due to their merits of miniaturized devices, easy integration, and low cost, showing great promising for point of care point-of-caring test. In order to achieve ultrasensitive detection of biomarkers, great effort focused on design of a sensitive FO-based biosensor on the aspect of novel FO probes and signal amplification strategies. Firstly, novel FO probes, including gating and new structure-based, were develop to adjust the light propagation and allow intensely interaction between the light and metal film or nanoparticles, which excites strong SPR or LSPR for sensitive biosensor. Then, nanomaterials on FO surface improved the intensity of electromagnetic fields or provided a good scaffold to modify with more recognition element for signal amplification. Nucleic acid circuits get rid of the limitation of the signal-to-target ratio of 1:1 and exhibited high efficiency to amplify the signal. These efforts have also led to the application of FO-SPR and LSPR sensors for detection of various targets, such as cells, nucleic acids, proteins, and small molecules. In the review, we summarized the important progress of the ultrasensitive FO-based biosensor about emerging FO probes and signal amplification strategies, also discussed its opportunities and challenges for the point-of-caring test. The review aims to promote the application of the FO-SPR and LSPR from experiments to real samples.

Electromechanically reconfigurable plasmonic nanoslits for efficient nano-opto-electro-mechanical tuning

Plasmonic metamaterials with strong localized surface plasmon resonances (LSPRs) have been improved by incorporating a nano-opto-electro-mechanical system (NOEMS) for tunable optical and electrical responses. However, conventional NOEMS devices suffer from the inefficient free-space coupling due to the limited design of reconfigurable antennas and the low optical tunability due to electrostatic pull-in of moving parts. In this paper, we propose efficient mid-infrared plasmonic nanoslits with variable nanometer-sized gaps giving rise to broad optical tunability. Our finite element method (FEM) analysis shows that by applying a voltage bias to asymmetric nanoslits supported on dielectric pillars, the gap width can be increased by more than 60 nm from an initial 1 nm. The large change in gap width results in a significant spectral shift in reflectance, while maintaining strong free-space coupling and a constant full width at half maximum (FWHM). We also analyze the effect of geometrical parameters on the nanometer-sized gap width and optical responses. Our nanoslits with simple geometry resulting in efficient optical coupling show promise for improving active metasurfaces and electromechanically tunable plasmonic devices.

Enhancing Silicon Solar Cell Performance Using a Thin-Film-like Aluminum Nanoparticle Surface Layer.

Solar cells play an increasing role in global electricity production, and it is critical to maximize their conversion efficiency to ensure the highest possible production. The number of photons entering the absorbing layer of the solar cell plays an important role in achieving a high conversion efficiency. Metal nanoparticles supporting localized surface plasmon resonances (LSPRs) have for years been suggested for increasing light in-coupling for solar cell applications. However, most studies have focused on materials exhibiting strong LSPRs, which often come with the drawback of considerable light absorption within the solar spectrum, limiting their applications and widespread use. Recently, aluminum (Al) nanoparticles have gained increasing interest due to their tuneable LSPRs in the ultraviolet and visible regions of the spectrum. In this study, we present an ideal configuration for maximizing light in-coupling into a standard textured crystalline silicon (c-Si) solar cell by determining the optimal Al nanoparticle and anti-reflection coating (ARC) parameters. The best-case parameters increase the number of photons absorbed by up to 3.3%. We give a complete description of the dominating light-matter interaction mechanisms leading to the enhancement and reveal that the increase is due to the nanoparticles optically exhibiting both particle- and thin-film characteristics, which has not been demonstrated in earlier works.