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We investigate the enhancement in the efficiency of organic bulk heterojunction solar cells enabled by plasmonic excitation of Ag nanoparticles (NPs) of different diameters (10, 20, and 30 nm), randomly incorporated within an optical spacing layer of TiO 2 placed between the organic medium and the Ag cathode. Such structures significantly increase the optical absorption and the photocurrent within the device system, leading to a power conversion efficiency of more than 4%, over 2.5 times that of the control bulk heterojunction cell. This corresponds to a 61% increase in J SC and a 6.3% in fill factor. 3D Finite-difference time-domain simulations were utilized to investigate the plasmonic field coupling within the nanogap medium of TiO 2 . They show that coupling between the Ag nanoparticle and the Ag thin film cathode extends the wavelength range of the local field enhancement beyond that obtained for isolated NPs, providing a better overlap with the absorption spectrum of the organic medium., Competing Interests: The authors declare no competing financial interest., (© 2025 The Authors. Published by American Chemical Society.)

The coupling between sub-bandgap defect states and surface plasmon resonances in Au nanoparticles and its effects on the photoconductivity performance of TiO 2 are investigated in both the ultraviolet (UV) and visible spectrum. Incorporating a 2 nm gold nanoparticle layer in the photodetector device architecture creates additional trapping pathways, resulting in a faster current decay under UV illumination and a significant enhancement in the visible photocurrent of TiO 2 , with an 8-fold enhancement of the defects-related photocurrent. We show that hot electron injection (HEI) and plasmonic resonance energy transfer (PRET) jointly contribute to the observed photoconductivity enhancement. In addition to shedding light on the below-band-edge photoconductivity of TiO 2 , our work provides insight into new methods to probe and examine the surface defects of metal oxide semiconductors using plasmonic resonances., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

The development of a long-range and efficient Förster resonance energy transfer (FRET) process is essential for its application in key enabling optoelectronic and sensing technologies. Via controlling the delocalization of the donor's electric field and Purcell enhancements, we experimentally demonstrate long-range and high-efficiency Förster resonance energy transfer using a plasmonic nanogap formed between a silver nanoparticle and an extended silver film. Our measurements show that the FRET range can be extended to over 200 nm while keeping the FRET efficiency over 0.38, achieving an efficiency enhancement factor of ∼10 8 with respect to a homogeneous environment. Reducing Purcell enhancements by removing the extended silver film increases the FRET efficiency to 0.55, at the expense of the FRET rate. We support our experimental findings with numerical calculations based on three-dimensional finite difference time-domain calculations and treat the donor and acceptor as classical dipoles. Our enhanced FRET range and efficiency structures provide a powerful strategy to develop novel optoelectronic devices and long-range FRET imaging and sensing systems., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Hyperbolic metaparticles have emerged as the next step in metamaterial applications, providing tunable electromagnetic properties on demand. However, coupling of optical modes in hyperbolic meta-antennas has not been explored. Here, we present in detail the magnetic and electric dipolar modes supported by a hyperbolic bowtie meta-antenna and clearly demonstrate the existence of two magnetic coupling regimes in such hyperbolic systems. The coupling nature is shown to depend on the interplay of the magnetic dipole moments, controlled by the meta-antenna effective permittivity and nanogap size. In parallel, the meta-antenna effective permittivity offers fine control over the electrical field spatial distribution. Our work highlights new coupling mechanisms between hyperbolic systems that have not been reported before, with a detailed study of the magnetic coupling nature, as a function of the structural parameters of the hyperbolic meta-antenna, which opens the route toward a range of applications from magnetic nanolight sources to chiral quantum optics and quantum interfaces.

Förster resonance energy transfer (FRET) is a fundamental phenomenon in photosynthesis and is of increasing importance for the development and enhancement of a wide range of optoelectronic devices, including color-tuning LEDs and lasers, light harvesting, sensing systems, and quantum computing. Despite its importance, fundamental questions remain unanswered on the FRET rate dependency on the local density of optical states (LDOS). In this work, we investigate this directly, both theoretically and experimentally, using 30 nm plasmonic nanogaps formed between a silver nanoparticle and an extended silver film, in which the LDOS can be controlled using the size of the silver nanoparticle. Experimentally, uranin-rhodamine 6G donor-acceptor pairs coupled to such nanogaps yielded FRET rate enhancements of 3.6 times. This, combined with a 5-fold enhancement in the emission rate of the acceptor, resulted in an overall 14-fold enhancement in the acceptor's emission intensity. By tuning the nanoparticle size, we also show that the FRET rate in those systems is linearly dependent on the LDOS, a result which is directly supported by our finite difference time domain (FDTD) calculations. Our results provide a simple but powerful method to control FRET rate via a direct LDOS modification.

Alignment of metal-organic framework (MOF) crystals has previously been performed via careful control of oriented MOF growth on substrates, as well as by dynamic magnetic alignment. We show here that bromobenzene-suspended microrod crystals of the MOF NU-1000 can also be dynamically aligned via electric fields, giving rise to rapid electrooptical responses. This method of dynamic MOF alignment opens up new avenues of MOF control which are important for integration of MOFs into switchable electronic devices as well as in other applications such as reconfigurable sensors or optical systems.

We study the thiophene-based oligomer poly[2,7-(9,9-bis(2'-ethylhexyl)fluorene)-alt-2,5-terthiophene] (PF3T) in solution and when dispersed at low concentration into a polynorbornene matrix. We find that at high concentration in solution the 0-0 electronic transition observed in fluorescence is suppressed, a result indicative of the formation of weakly coupled H-aggregates. At low concentration in a polymer matrix, emission from both single molecules and molecular aggregates is observed. We find that the fluorescence spectra of most PF3T emitters are composed of a number of relatively narrow emission features, indicating that the emission usually occurs from multiple chromophores. A small number of PF3T molecules are however characterized by single chromophore emission, spectral blinking, and narrowed emission peaks.

We have fabricated an L3 optical nanocavity operating at visible wavelengths that is coated with a thin-film of a fluorescent molecular-dye. The cavity was directly fabricated into a pre-etched, free-standing silicon-nitride (SiN) membrane and had a quality factor of Q = 2650. This relatively high Q-factor approaches the theoretical limit that can be expected from an L3 nanocavity using silicon nitride as a dielectric material and is achieved as a result of the solvent-free cavity-fabrication protocol that we have developed. We show that the fluorescence from a red-emitting fluorescent dye coated onto the cavity surface undergoes strong emission intensity enhancement at a series of discrete wavelengths corresponding to the cavity modes. Three dimensional finite difference time domain (FDTD) calculations are used to predict the mode structure of the cavities with excellent agreement demonstrated between theory and experiment.

Electron-hole pair formation at titania surfaces leads to the formation of reactive species that degrade organic materials. Here, we describe the degradation of self-assembled monolayers of alkylphosphonic acids on the native oxide of titanium following exposure to UV light. The rate of degradation was found to decrease as the length of the adsorbate molecule increased. Increasing order in the monolayer, resulting from the enhanced dispersion forces between longer adsorbates, impedes the progress of oxygen-containing molecules to the oxide surface and slows the rate of oxidation. Rates of degradation on titanium oxide are substantially greater than rates of degradation on aluminum oxide because of the photocatalytic effect of the titanium oxide substrate. Micrometer-scale patterns may be fabricated readily using a UV laser in conjunction with a mask, and nanometer-scale patterns may be fabricated using a scanning near-field optical microscope coupled to a UV laser. Photodegraded adsorbates may be replaced by contrasting molecules to yield chemical contrast. Such patterned materials have been utilized to fabricate patterns from polymer nanoparticles. The resist character is switchable--at lower exposures, the monolayer behaves as a positive tone resist, but at higher exposures, it exhibits negative tone behavior. Patterned samples may also be utilized as resists for solution-phase etching of the underlying substrate.