Tungsten Diselenide Nanoparticles Produced via Femtosecond Ablation for SERS and Theranostics Applications.

Due to their high refractive index, record optical anisotropy and a set of excitonic transitions in visible range at a room temperature, transition metal dichalcogenides have gained much attention. Here, we adapted a femtosecond laser ablation for the synthesis of WSe nanoparticles (NPs) with diameters from 5 to 150 nm, which conserve the crystalline structure of the original bulk crystal. This method was chosen due to its inherently substrate-additive-free nature and a high output level.

Leveraging Femtosecond Laser Ablation for Tunable Near-Infrared Optical Properties in MoS-Gold Nanocomposites.

Transition metal dichalcogenides (TMDCs), particularly molybdenum disulfide (MoS), have gained significant attention in the field of optoelectronics and photonics due to their unique electronic and optical properties. The integration of TMDCs with plasmonic materials allows to tailor the optical response and offers significant advantages for photonic applications. This study presents a novel approach to synthesize MoS-Au nanocomposites utilizing femtosecond laser ablation in liquid to achieve tunable optical properties in the near-infrared (NIR) region.

Real-time assessment of hypnotic depth, using an EEG-based brain-computer interface: a preliminary study.

Objective: Hypnosis can be an effective treatment for many conditions, and there have been attempts to develop instrumental approaches to continuously monitor hypnotic state level ("depth"). However, there is no method that addresses the individual variability of electrophysiological hypnotic correlates. We explore the possibility of using an EEG-based passive brain-computer interface (pBCI) for real-time, individualised estimation of the hypnosis deepening process.

Molecular Structure-Intrinsic Photostability Relationships for a Series of Conjugated Polymers: Backbone Substitution Matters!

Herein, we present an efficient approach for screening the intrinsic photostability of organic absorber materials used in photovoltaic applications. Using a series of structurally related conjugated polymers and a set of complementary techniques, we established important "material structure-photostability" relationships. In particular, we have revealed that the introduction of alkoxy, thioalkyl, and fluorine substituents adversely affects the material photostability.

Resist or Oxidize: Identifying Molecular Structure-Photostability Relationships for Conjugated Polymers Used in Organic Solar Cells.

Although organic solar cells have started to demonstrate competitive power conversion efficiencies of >18 %, their operational lifetimes remain insufficient for wide practical use and the factors influencing the photostability of absorber materials and completed devices are still not completely understood. A systematic study of two series of structurally similar [XTBT] and [XTTBTBTT] polymers (16 structures in total) reveals the building blocks that enable the highest material stability towards photooxidation: fluorene, silafluorene, carbazole, diketopyrrolopyrrole, and isoindigo. Furthermore, a direct correlation is evident between the electronic properties of the conjugated polymers and their reactivity towards oxygen.

Impressive Radiation Stability of Organic Solar Cells Based on Fullerene Derivatives and Carbazole-Containing Conjugated Polymers.

We explored the radiation stability of carbazole-based electron-donor conjugated polymers, acceptor fullerene derivative [60]PCBM, and their blends as active layer components of organic solar cells. An exposure to γ rays induced evident degradation effects in bulk samples of the pristine fullerene acceptor ([60]PCBM) and two investigated electron-donor conjugated polymers: PCDTBT and PCDTTBTBTT. The most severe radiation damage occurred in [60]PCBM as can be concluded from the significant losses in open circuit voltage, fill factor, and efficiency of photovoltaic (PV) devices comprising the exposed fullerene acceptor.