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Mayte Gómez-Castaño

Publications and source records attributed to Mayte Gómez-Castaño.

2 recordsLinked to original sources

Band-Selective LDOS Engineering of Yb/Er Upconversion: an Electromagnetic-Kinetic Diagnostic Framework

A persistent challenge in plasmonic upconversion is decoupling pump-field enhancement from emission-side local-density-of-optical-states (LDOS) engineering to achieve selective band manipulation. Here, we show that a corrugated SU8/Au/Al2O3 grating coated with a NaYF4:Yb/Er upconversion nanoparticle (UCNP) monolayer realizes a truly band-selective platform. A broad plasmonic resonance near 670 nm modulates the red Er 3 + 3+ decay rate by $\pm$15% as a function of the Al2O3 spacer thickness, while leaving the green transition experimentally invariant (< 1% change). Simultaneously, the 980 nm pump field is monotonically suppressed below free-space levels, ensuring that steady-state and time-resolved observables cleanly probe the emission-side LDOS without pump interference. We analyze this system using a coupled electromagnetic-kinetic framework that integrates finite-difference time-domain (FDTD) calculations of Purcell factors and pump fields with a six-level Yb/Er rate-equation model. The framework quantitatively reproduces the 670 nm plasmonic resonance, the red-band decay-rate modulation, and the monotonic decrease of the green/red intensity ratio. Crucially, the model serves as a powerful diagnostic tool: it overpredicts a green-band rate reduction, but systematic parametric testing rules out geometric (apex smoothing) and material (grain-boundary damping, interband loss) imperfections as the cause. Instead, it isolates the residual discrepancy to measurement-versus-model factors (finite-aperture angular averaging) and missing non-radiative kinetic channels, establishing a clear roadmap for the rational design and validation of future plasmonic-UCNP architectures.

physics.optics↗

Energy transfer and interference by collective electromagnetic coupling

The physics of collective optical response of molecular assemblies, pioneered by Dicke in 1954, has long been at the center of theoretical and experimental scrutiny. The influence of the environment on such phenomena is also of great interest due to various important applications in e.g. energy conversion devices. In this manuscript we demonstrate both experimentally and theoretically the spatial modulations of the collective decay rates of molecules placed in proximity to a metal interface. We show in a very simple framework how the cooperative optical response can be analyzed in terms of intermolecular correlations causing interference between the response of different molecules and the polarization induced on a nearby metallic boundary and predict similar collective interference phenomena in excitation energy transfer between molecular aggregates.

cond-mat.mes-hall↗