Textiles, in combination with advances in materials and design, offer exciting new possibilities for human and environmental interaction, including biometric and touch-based sensing. Previous fabric-based or flexible touch sensors have generally required a large number of sensing electrodes positioned in a dense XY grid configuration and a multitude of wires. This paper investigates the design and manufacturing of a planar (two-dimensional, XY location) touch fabric sensor with only two electrodes (wires) to sense both planar touch and pressure, making it ideal for applications with limited space/complexity for wiring. The proposed knitted structure incorporates a supplementary method of sensing to detect human touch on the fabric surface, which offers advantages over previous methods of touch localization through an efficient use of wire connections and sensing materials. This structure is easily manufactured as a single component utilizing flatbed knitting techniques and electrically conductive yarns. The design requires no embedded electronics or solid components in the fabric, which allows the sensor to be flexible and resilient. This paper discusses the design, fabrication, sensing methods, and applications of the fabric sensor in robotics and human-machine interaction, smart garments, and wearables, as well as the highly transdisciplinary approach pursued in developing medical textiles and flexible embedded sensors.

Here we discuss requirements for high performance and solution processable organic semiconductors, by presenting a systematic investigation of 7-alkyl-2-phenyl[1]benzothieno[3,2-b][1]benzothiophenes (Ph-BTBT-Cn ’s). We found that the solubility and thermal properties of Ph-BTBT-Cn ’s depend systematically on the substituted alkyl-chain length n. The observed features are well understood in terms of the change of molecular packing motif with n: The compounds with n ≤ 4 do not form independent alkyl chain layers, whereas those with n ≥ 5 form isolated alkyl chain layers. The latter compounds afford a series of isomorphous bilayer-type crystal structures that form two-dimensional carrier transport layers within the crystals. We also show that the Ph-BTBT-C10 afford high performance single-crystalline field-effect transistors the mobility of which reaches as high as 15.9 cm2/Vs. These results demonstrate a crucial role of the substituted alkyl chain length for obtaining high performance organic semiconductors and field-effect transistors.

Charge transport properties of pentacene have been investigated by a joint experimental and theoretical study. The growth of pentacene on the substrates shows mainly two different polymorphic phases, a bulk phase and a thin-film phase. The thin-film phase is crucial for the charge transport in two-terminal and three-terminal devices such as organic Schottky diodes and organic thin film transistors, respectively. Experimentally, mobility in two-terminal devices is less by five orders of magnitude than that in three-terminal devices. We show here that this difference can be explained on the basis of strong electronic coupling between molecular dimers located in the ab-plane and relatively weak coupling between the planes (along the c-axis).

The study of on-body energy harvesting is most often focused on improving and optimizing the energy harvester. However, other factors play a critical factor in the energy harvesting integration techniques of the harvester to close-to body materials of the wearable device. In addition, one must recognize the wide array of human factors and ergonomic factors that lead a variation of the energy harvesting. In this work, key affecting variables at varying on-body locations are investigated for commercial thermoelectric generators (TEGs) integrated within a textile-based wearable platform. For this study, a headband and an armband is demonstrated with five TEGs connected in series in a flexible form factor via Pyralux®. These platforms enable comparison of the amount of energy harvested from the forehead versus the upper arm during various external conditions and movement profiles, e.g. running, walking, and stationary for periods of up to 60 minutes. During these tests, ambient temperature, ambient humidity, accelerometry, and instantaneous power are recorded live during the activity and correlated to the energy harvested. Human factors such as skin temperature and application pressure were also analyzed. Our analysis demonstrates that vigorous movement can generate over 100 μW of instantaneous power from the headband and up to 35 μW from the armband. During the stationary movement profile, the instantaneous power levels of both the headband and the armband decreased to a negligible value. Our studies show that for higher intensities of movement, air convection on the cool side of the TEG is the dominating variable whereas the temperature gradient has a significant effect when the subject is stationary. This work demonstrates key materials and design factors in on-body thermoelectric energy harvesting that allows for a strategic approach to improving the integration of the TEGs.

This paper introduces the design and simulated operation of a capacitive hydration sensor for integration into textile-based electronics. The multilayer patch is composed of a textile layer and an attached series of serpentine-interdigitated electrodes. The model used for simulations incorporated this design onto a representative model of skin. The serpentine-interdigitated electrodes are electrodes for capacitive measurement of skin hydration. In this study, the capacitance change relative to skin hydration was simulated using finite element analysis. The simulation results suggest the fabric layer had little effect on the capacitance of the sensor. Furthermore, the frequency domain simulations indicated that the capacitance of the sensor decreased with increasing frequency, and the decrease in capacitance was more significant for the dry skin compared to the wet skin. Therefore, the variation in the capacitance value of the serpentine-interdigitated electrodes can be employed for continuous skin hydration detection.

Spectroscopic imaging and statistical analysis of NIR-to-visible upconversion luminescence (UCL) from β-NaYF4:Yb3+:Er3+ upconverting nanoparticles (UCNPs) supported on a series of random Ag nanowire aggregates reveals a density dependent UCL enhancement. Statistical analysis of the spectrally resolved upconversion images shows a non-linear dependence of upconversion luminescence enhancement with Ag nanowire surface coverage. A maximum average enhancement of 5.8× was observed for 58% surface coverage. Based on the empirically determined trend with density, it is estimated that up to 20× upconversion luminescence enhancement can be achieved at 100% surface coverage, even at high excitation intensity. This projection is commensurate with the 20× enhancement ratio observed for select locations within the imaged micro-ensemble. Time-resolved emission of the UC luminescence from UCNPs on the Ag nanowire aggregates confirms the surface plasmon effects on the UCNPs kinetics. Such Ag nanowire aggregates show potential as a scalable and relatively simple metal-enhanced upconversion substrate.

ErxYb(3-x)Q9 (1, x = 1, 2), NdYb2Q9 (2), NdEr2Q9 (3) and NdErYbQ9 (4), have been obtained through a simple molecular strategy, by controlling reactant stoichiometry. In 2-4, the templating effect of the molecular framework allows to control the metal distribution across the coordination sites where the central position is occupied by the larger Nd ion and the terminal ones by the almost vicariants Yb3+ and Er3+, drastically reducing molecular speciation. Remarkably, 4 represents the first example of a discrete molecular entity containing three different Ln ions simultaneously emitting in three different spectral regions in the NIR, upon single visible wavelength excitation. Highly transparent and homogeneous doped silica glasses have been prepared, which show the same optical properties of the incorporated complex in solution.

The luminescence of Tb-doped a-SiC:H thin films with different Tb concentrations under sub-bandgap photon excitation was investigated. Two independent processes were identified. The annealing induced activation of the Tb3+ and the inhibition of host-mediated non-radiative recombination paths. The integrated emission intensity is described by a rate equation model, considering these two. In this study, the luminescence enhancement with increasing annealing temperature is shown. The optimal Tb concentration and annealing temperature for the highest Tb-related light emission intensity is determined. Finally, a parameter proportional to the number of optically active ions is found through the aforementioned model.

The rare earth (RE) mineral loparite with the chemical composition (RE, Na, Sr, Ca)(Ti, Nb, Ta, Fe+3)O3 is the principal ore of the light rare earth elements (LREE) as well as niobium and tantalum. The enthalpies of formation of RE0.67-xNa3xTiO3 (RE = La, Ce) and Ca1-2xNaxLaxTiO3 from oxides and elements of lanthanum and cerium perovskites and their solid solutions have been obtained using high temperature oxide melt solution calorimetry. RE0.67-xNa3xTiO3 (RE = La, Ce) perovskites become more stable relative to oxide components as sodium content increases. Na0.5Ce0.5TiO3 and Na0.5La0.5TiO3 can be considered stable endmembers in natural loparite minerals. For perovskite solid solutions Ca1-2xNaxLaxTiO3, the enthalpies of formation from the constituent oxides $\Delta {\rm{H}}_{{\rm{f}},\,{\rm{ox}}}^^\circ$ become more exothermic with increasing Na+La content, suggesting a stabilizing effect of the substitution 2Ca2+ → Na+ + La3+ on the perovskite structure. The trend of increasing thermodynamic stability with decreasing structural distortion is similar to that seen in many other ABO3 perovskites.