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The patterning of composites with carbon-based additives of nanometer or micrometer size was studied by the precise modification of material surfaces using laser technology. Initially, the composites are electrical insulators, but we can make them conductive by selective patterning; this process allows us to create conductive tracks within seconds, with a sheet resistance that can be adjusted over a wide range, from 108 Ω/sq down to 2.5 Ω/sq. The additives used include graphene nanoplatelets, graphene oxide nanosheets, and aramid fibers. By conducting microscopic and spectroscopic characterizations before and after laser treatment, we can distinguish between two different processes that lead to electrical conduction: (a) localized increase in the concentration of conductive additives or (b) localized reduction and pyrolysis of insulating additives. To demonstrate the versatility and usefulness of this technique in different fields of application, such as automotive, we fabricate three different devices on polyurethane: a heater, a proximity sensor, and an amperometric sensor for detecting biological analytes. [ABSTRACT FROM AUTHOR]

Fluorescent nanodiamonds (FNDs) containing quantum defects enable the optical measurement of electromagnetic fields and temperature and are among the most developed nanoscale quantum sensors today. Yet, for many applications in biomedicine and beyond, FNDs must be integrated into biocompatible substrates that preserve FND sensitivity and bring FNDs within nanoscale distance of their sensing target. At the same time, the high excitation light intensity required for most quantum sensing protocols remains a major challenge for applications in biomedicine. Here, it is shown that FNDs embedded in polyvinyl‐alcohol (PVA) fibers are a powerful 3D platform for nanoscale quantum sensing via light guiding. First, it is demonstrated that biocompatible PVA fibers can guide light to excite FNDs >10 µm from the excitation beam. Using this light‐guiding‐enabled excitation, optically detected magnetic resonance (ODMR) and T1 spin relaxometry measurements are performed using the nitrogen‐vacancy (NV) center in FNDs. Through ODMR thermometry, it is shown that light‐guiding‐enabled excitation mitigates light‐induced heating. Finally, the quantum sensing capability of the platform is established by detecting paramagnetic gadolinium in a dry and aqueous environment using T1 relaxometry of the NV center in FNDs. These results pave the way for light‐guiding‐enabled optical quantum sensing in biomedicine using nanodiamond‐doped biosubstrates. [ABSTRACT FROM AUTHOR]

Here, we exploited the UV light and thermal triggered E ↔ Z photoisomerization of an azobenzene compound to fabricate multimodal readable and rewritable data matrix based devices. We first demonstrated that the UV light sensing capabilities can be simultaneously monitored by the change in optical, spectroscopic, and electrical properties. Then we exploited this capability by integrating tetra(azobenzene)methane crystals in a micrometric TAG whose information can be modified and repristinated by local UV treatment and thermal annealing. The system was characterized by polarized optical microscopy, Raman spectroscopy, conductive atomic force microscopy and Kelvin Probe Force Microscopy. [ABSTRACT FROM AUTHOR]

The article titled "Quantum Sensing and Light Guiding with Fluorescent Nanodiamond-Doped PVA Fibers" in Advanced Optical Materials explores the potential of using fluorescent nanodiamonds for quantum sensing. The study demonstrates that the red fluorescence of nanodiamonds can be stimulated by light transmitted through electrospun polymer fibers. This fluorescence can be utilized for quantum sensing of local temperature and the presence of nearby magnetic molecules. The findings suggest the development of a biocompatible quantum sensing platform with applications in biology and medicine. [Extracted from the article]

A detailed experimental investigation of the effects giving rise to the magnetic energy level structure in the vicinity of the level crossing (LC) at low temperature is reported for the open antiferromagnetic molecular ring Cr8Zn. The study is conducted by means of thermodynamic techniques (torque magnetometry, magnetization and specific heat measurements) and microscopic techniques (nuclear magnetic resonance line width, nuclear spin lattice, and spin-spin relaxation measurements). The experimental results are shown to be in excellent agreement with theoretical calculations based on a minimal spin model Hamiltonian, which includes a Dzyaloshinskii-Moriya interaction. The first ground state level crossing at μ0Hc1 = 2.15 T is found to be an almost true LC while the second LC at μ0Hc2 = 6.95 T has an anti-crossing gap of Δ12 = 0.19 K. In addition, both NMR and specific heat measurements show the presence of a level anti-crossing between excited states at μ0H = 4.5 T as predicted by the theory. In all cases, the fit of the experimental data is improved by introducing a distribution of the isotropic exchange couplings (J), i.e., using a J strain model. The peaks at the first and second LCs in the nuclear spin-lattice relaxation rate are dominated by inelastic scattering and a value of Γ ~ 1010 rad/s is inferred for the life time broadening of the excited state of the open ring, due to spin phonon interaction. A loss of NMR signal (wipe-out effect) is observed for the first time at LC and is explained by the enhancement of the spin-spin relaxation rate due to the inelastic scattering. [ABSTRACT FROM AUTHOR]

Here is reported an expedient synthesis implementing enabling technologies of a family of thiophene-based heptamers alternating electron donor (D) and acceptor (A) units in a D–A′–D–A–D–A′–D sequence. The nature of the peripheral A groups (benzothiadiazole vs. thienopyrrole-dione vs. thiophene-S,S-dioxide) and the strength of the donor units (alkyl vs. thioalkyl substituted thiophene ring) have been varied to finely tune the chemical-physical properties of the D–A oligomers, to affect the packing arrangement in the solid-state as well as to enhance the photovoltaic performances. The optoelectronic properties of all compounds have been studied by means of optical spectroscopy, electrochemistry, and density functional theory calculations. Electrochemical measurements and Kelvin probe force microscopy (KPFM) predicted a bifunctional behaviour for these oligomers, suggesting the possibility of using them as donor materials when blended with PCBM, and as acceptor materials when coupled with P3HT. Investigation of their photovoltaic properties confirmed this unusual characteristic, and it is shown that the performance can be tuned by the different substitution pattern. Furthermore, thanks to their ambivalent character, binary non-fullerene small-molecule organic solar cells with negligible values of HOMO and LUMO offsets were also fabricated, resulting in PCEs ranging between 2.54–3.96%. [ABSTRACT FROM AUTHOR]

Contact resistance effects in n-type organic field-effect transistors (OFETs) based on perylene-diimide thin films and monolayer CVD graphene electrodes have been investigated by using Scanning Kelvin Probe Force Microscopy (SKPFM). SKPFM voltage profiles were acquired as a function of the applied drain–source (Vds) and gate–source (Vgs) voltages and in the temperature range between 300 and 360 K. The results were compared with those obtained for hybrid devices bearing contemporarily a gold and a graphene electrode, in order to highlight the specific behaviors of the graphene/organic and gold/organic interfaces. Despite the fact that overall electrical performances of devices based on gold and graphene contacts are fully comparable, the SKPFM analysis demonstrates unambiguously that the physical mechanisms driving the charge injection and extraction phenomena are distinctive based on the electrode type. While for OFETs with gold electrodes, the RC effect is mainly ascribable to the degraded quality of the charge transport in the semiconducting film regions close to the electrodes, for graphene-based devices, it is related to the presence of a Schottky-like barrier at the injecting electrode. [ABSTRACT FROM AUTHOR]

Future applications of molecular units in quantum information technologies require a fine control at the single molecule level. This includes the choice of each functional element, the intramolecular interaction and the robustness of molecules when dispersed on a substrate. Keeping these goals in mind, we designed and synthesized a heterometallic phthalocyaninato-complex including two different lanthanides in each moiety, namely [PcDyPcTbPc*] (Pc being phthalocyanines; and Pc* being 2,3,9,10,16,17,23,24-octahexyl-substituted phthalocyanines). Full magnetic characterization was performed down to the mK temperature range on bulk microcrystals by means of AC susceptibility, DC magnetization (including microSQUID) and specific heat measurements. A weak, yet sizeable, interaction between the two lanthanides is clearly detected by different techniques, altering the magnetic behavior of the single lanthanide as observed in the parent [LnPc2] complexes. Isolated [PcDyPcTbPc*] molecules dispersed on HOPG and the Au surface by liquid phase deposition are proven to maintain their main chemical and magnetic features by combined XPS, XAS and XMCD analysis and to lie with one Pc ligand flat to the surface. Opening of a small but sizable hysteresis loop at 1.8 K is directly observed on both Tb and Dy sites proving the retention of magnetization at the single molecule level. [ABSTRACT FROM AUTHOR]

Proving the preservation of functionality at the molecular scale is still a major challenge, both for the choice of suitable derivatives and protocols and for the employed experimental tools and methods. By using a combined scanning probe (AFM and STM) and spectroscopic methodology (XPS, XAS and XMCD), it is shown that Gd4M8 derivatives (with M = Zn2+, Ni2+) are robust molecular units which preserve their electronic, magnetic, and thermodynamic properties when deposited on a metallic surface. Namely, entropy variation Δ S = [ S(6 T) - S(0 T)] exceeding 8 R (20 J kg−1 K−1) at 4 K in isolated Gd4Ni8 molecules dispersed on Au(111) surface is measured and a viable route to exploit large magnetocaloric effect at single molecule level is shown. [ABSTRACT FROM AUTHOR]

The article discusses a study that investigates the hysteretic behavior in vacuum deposited submonolayer of single ion magnets sublimated on pyrolytic graphite with the help of X-ray absorption spectroscopy and X-ray magnetic circular dichroism. Topics discussed include field dependence of the magnetization in central lanthanide ion at low temperature, integration of organic materials into spintronic devices and remanent magnetization of single ion magnets.

The ability to assemble weakly interacting subsystems is a prerequisite for implementing quantum information processing and generating controlled entanglement. In recent years, molecular nanomagnets have been proposed as suitable candidates for qubit encoding and manipulation. In particular, antiferromagnetic Cr7Ni rings behave as effective spin-1/2 systems at low temperature and show long decoherence times. Here, we show that these rings can be chemically linked to each other and that the coupling between their spins can be tuned by choosing the linker. We also present calculations that demonstrate how realistic microwave pulse sequences could be used to generate maximally entangled states in such molecules. [ABSTRACT FROM AUTHOR]

An unusually large magnetocaloric effect for the temperature region below 10 K is found for the Fe14 molecular nanomagnet. This is to large extent caused by its extremely large spin S ground state combined with an excess of entropy arising from the presence of low-lying excited S states. We also show that the highly symmetric Fe14 cluster core, resulting in small cluster magnetic anisotropy, enables the occurrence of long-range antiferromagnetic order below TN=1.87 K. [ABSTRACT FROM AUTHOR]