Abstract
The phase-matching conditions for exciting surface plasmon resonances (SPR) in plasmonic films are typically satisfied via prism, optical fibers or grating-assisted coupling. We recently showed that plasmonic nanospheres can act as local emitters, exciting SPR waves on thin films-termed nanoparticle-induced SPR (NPI-SPR). This structure holds promise for sensing, but the effects of optical fiber geometry and nanoparticle anisotropy on the response were unexplored. This study examines these factors, showing that an etched multimode fiber with a 200 mu m core diameter, taper ratio of 4, and etching angle of 20 degrees optimizes interaction with plasmonic nanoparticles. Tuning the nanoparticle aspect ratio from 1 to 3 shifts the NPI-SPR band from 780 to 1580 nm, with excitation highly dependent on the incident light angle. Notably, for light incident parallel to the film plane, a refractive index sensitivity exceeding 1000 nm/RIU is achieved. This efficient light emission combines the field locality enhancements of plasmonic nanoparticle-on-film structures with the emission efficiency of plasmonic nanoantennas, advancing plasmonic optical fiber chemical and biosensors.

Abstract
Reinforced concrete structures form the backbone of civil infrastructure due to their durability, longevity, affordability, and availability. However, aging concrete poses challenges, with decay often beginning internally and becoming visible only at advanced stages, leading to costly repairs, restricted functionality, and safety risks. To address these challenges, sensors are crucial for enhancing infrastructure resilience and optimizing repairs. This study employs multimode optical fibers to monitor concrete curing, water ingress, relative humidity (RH), cement paste carbonation, and rebar corrosion. Four sensors monitor changes in reflection at the fiber tip of a 600 mu m multimode fiber (MMF) using LEDs and photodiodes, connected via a fiber bundle containing two 200 mu m MMF. Variations in the refractive index around the fiber tip are used to monitor water throughout the concrete lifecycle, including curing, RH changes and water intrusion. Colorimetric changes in a cement paste layer and an iron-thin film are used to monitor carbonation and corrosion. The curing sensor is temperature-independent and correlates strongly with cumulative heat release from cement hydration (R=0.95). The RH sensor monitors up to and beyond 100% RH, detecting water intrusion. The corrosion sensor detects early corrosion stages and distinguishes between reflection losses from corrosion and mechanical changes. The layer of cement paste for carbonation monitoring increases reflected intensity by 17% due to carbonation, with 63% of the increase occurring in 80 minutes in a 3% CO2 atmosphere. The broad monitoring scope and low implementation cost make this sensor a unique option among commercially available solutions for structural health monitoring of reinforced concrete.

Abstract
This study investigates the fabrication of plasmonic optical fiber sensors for glyphosate detection, employing silver thin film coatings deposited via the Tollens' reaction and further enhanced with protective gold plating. Silver films were produced through electroless deposition, forming rough plasmonic surfaces with localized hotspots that amplify the electromagnetic field. Surface roughness effects on the creation of hotspots were first evaluated numerically using the finite element method (FEM) and later experimentally assessed the impact on optical response. Furthermore, to address the inherent susceptibility of silver to oxidation and corrosion, a gold plating was applied using the Kirkendall effect, selectively replacing surface silver atoms with gold. This approach significantly improved the chemical stability of the sensors while preserving their plasmonic properties. This configuration was applied in developing a biosensor, using aptamers, for detecting glyphosate in concentrations ranging from 10(-1) to 10(4) mu g/L. The results demonstrated a sensitivity of 25.08 +/- 0.22 nm/(mu g/L) and a limit of detection (LOD) of 0.04 mu g/L, nearly ten times lower than the European Union's safety limit for glyphosate. Experimental results highlight the potential of this fabrication approach for developing sensitive, stable, and scalable plasmonic sensors tailored for environmental and agricultural monitoring applications.

Abstract
Abstract Inductively coupled plasma-mass spectrometry analysis was conducted to examine the geochemical composition of K-feldspars from various aplite-pegmatites in the Barroso-Alvão field, focusing on the differences between Li-rich and Li-barren aplite-pegmatites. The study revealed significant variations in the concentrations of minor and trace elements (Rb, Tl, Li, Ga, Pb, Cs, Ba, Be, Ta, and Sn) present in the K-feldspars of Li-barren, spodumene-rich, and petalite-rich aplite-pegmatites. The data also indicate a geographical trend in both mineralogy and geochemistry across the aplite-pegmatites of the Barroso-Alvão field. Li-barren aplite-pegmatites are more concentrated in the southeast, spodumene-rich dominate the center, and petalite-rich varieties are more common in the northwest. Additionally, portable X-ray fluorescence analysis was performed on the crystals of the same samples to evaluate the feasibility of in situ geochemical analysis of K-feldspars, aiming to determine whether an aplite-pegmatite can be quickly identified as Li-rich. This approach seeks to provide a rapid field assessment of whether an aplite-pegmatite justifies further exploration for Li mining. Notably, the trace amounts of Li, Sn, P, and Ta found in K-feldspars are likely due to mineral inclusions of spodumene, cassiterite, apatite, and columbite–tantalite minerals, as observed petrographically in one of these Li-rich aplite-pegmatites.

Abstract
Heritage preservation requires innovative sensing technologies to analyze their chemical composition while minimizing damage. This study introduces a Laser-induced Breakdown Spectroscopy (LIBS) system featuring a fiber laser source and optical fiber-based collection system for the analysis of heritage ceramics. Comparative experiments with a conventional Nd:YAG laser LIBS system highlight the advantages and trade-offs of the fiber laser system in terms of ablation capability, spectral mapping, and depth profiling. Results were validated against X-ray Fluorescence (XRF). Experiments demonstrate minimal surface alteration and high-quality spectral data for elements such as Pb, Fe, Zn, Sb, Mn, Ti Na, Ba and Ca. The compact design and good results position this system as a transformative tool for heritage conservation.

Abstract
Solid-state batteries are prominent in today's research landscape due to their advantages in capacity and safety. This work explores anode-less all-solid-state batteries, a configuration with industrial benefits as it avoids handling alkali metal anodes, albeit with room for improvement. To elucidate the intricacies of these batteries, Laser-Induced Breakdown Spectroscopy (LIBS) served as a pivotal analytical tool, primarily focusing on the negative current collector surface where Li+ nucleation occurs from the Li-rich electrolyte. The use of a fiber-laser for breakdown spectroscopy offers advantages over conventional lasers by producing high beam quality, enabling minimal spot size, and ensuring excellent spatial resolution. LIBS is an asset to verify Li presence, discerning its source, assessing nucleation and distinguishing it from electrolyte-derived Li. For instance, in this work utilizing Li2.99Ba0.005ClO as the electrolyte, LIBS is crucial to elucidate the relationship between Li and other elements like Cl, Zn, or Fe, shedding light on key battery performance aspects. LIBS demonstrated a high potential for verifying in situ Li metal nucleation in anode-less cells. This study highlights its effectiveness in conceptual and product development and advanced quality testing. The application of a clustering method enhanced result interpretability and the distinction between electrolyte and in situ anode regions.