Nanofiber-Reinforced Silver Nanowires Network as a Robust, Ultrathin, and Conformable Epidermal Electrode for Ambulatory Monitoring of Physiological Signals.

Extremely soft and thin electrodes with high skin conformability have potential applications in wearable devices for personal healthcare. Here, a submicrometer thick, highly robust, and conformable nanonetwork epidermal electrode (NEE) is reported. Electrospinning of polyamide nanofibers and electrospraying of silver nanowires are simultaneously performed to form a homogeneously convoluted network in a nonwoven way. For a 125 nm thick NEE, a low sheet resistance of ≈4 Ω sq-1 with an optical transmittance of ≈82% is achieved. Due to the nanofiber-based scaffold that undertakes most of the stress during deformation, the electric resistance of the NEE shows very little variation; less than 1.2% after 50 000 bending cycles. The NEE can form a fully conformal contact to human skin without additional adhesives, and the NEE shows a contact impedance that is over 50% lower than what is found in commercial gel electrodes. Due to conformal contact even under deformation, the NEE proves to be a stable, robust, and comfortable approach for measuring electrocardiogram signals, especially when a subject is in motion. These features make the NEE promising for use in the ambulatory measurement of physiological signals for healthcare applications.

A Flexible and Ultra-Highly Sensitive Tactile Sensor through a Parallel Circuit by a Magnetic Aligned Conductive Composite.

The development of flexible electronic skins with high performance and multifunctional sensing capabilities is of great significance for applications ranging from healthcare monitoring to artificial intelligence. To mimic and surpass the high-gauge-factor sensing properties of human skin, structure design and appropriate material selection of sensors are both essentially required. Here, we present an efficient, low-cost fabrication strategy to construct an ultra-highly sensitive, flexible pressure sensor by embedding the aligned nickel-coated carbon fibers (NICFs) in a polydimethylsiloxane (PDMS) substrate. Our design substantially contributes to ultrahigh sensitivity through the parallel circuit formed by aligned NICFs as well as surface spinosum microstructure molded by sandpaper. As a result, the sensor exhibits excellent sensitivity (15 525 kPa-1), a fast response time (30 ms), and good stability over 3000 loading-unloading cycles. Furthermore, these superior sensing properties trigger applications in water quality and wave monitoring in conjunction with mechanical flexibility and robustness. As a precedent for adjusting the sensitivities of the sensor, the NICFs/PDMS sensor provides a promising method for multiscenario healthcare monitoring, multiscale pressure spatial distribution, and human-machine interfacing.

Ultracomfortable Hierarchical Nanonetwork for Highly Sensitive Pressure Sensor.

Skin sensors are of paramount importance for flexible wearable electronics, which are active in medical diagnosis and healthcare monitoring. Ultrahigh sensitivity, large measuring range, and high skin conformability are highly desirable for skin sensors. Here, an ultrathin flexible piezoresistive sensor with high sensitivity and wide detection range is reported based on hierarchical nanonetwork structured pressure-sensitive material and nanonetwork electrodes. The hierarchical nanonetwork material is composed of silver nanowires (Ag NWs), graphene (GR), and polyamide nanofibers (PANFs). Among them, Ag NWs are evenly interspersed in a PANFs network, forming conductive pathways. Also, GR acts as bridges of crossed Ag NWs. The hierarchical nanonetwork structure and GR bridges of the pressure-sensitive material enable the ultrahigh sensitivity for the pressure sensor. More specifically, the sensitivity of 134 kPa-1 (0-1.5 kPa) and the low detection of 3.7 Pa are achieved for the pressure sensor. Besides, the nanofibers act as a backbone, which provides effective protection for Ag NWs and GR as pressure is applied. Hence, the pressure sensor possesses an excellent durability (>8000 cycles) and wide detection range (>75 kPa). Additionally, ultrathin property (7 µm) and nanonetwork structure provide high skin conformability for the pressure sensor. These superior performances lay a foundation for the application of pressure sensors in physiological signal monitoring and pressure spatial distribution detection.

Highly conductive, stretchable, and breathable epidermal electrode based on hierarchically interactive nano-network.

Stretchable electrodes have a crucial impact on the development of flexible electronic systems. Most conventionally blended nanocomposite electrodes are incapable of achieving high stretchability, breathability, or durability. In this work, a highly conductive, breathable, and stretchable epidermal electrode (SEE) is demonstrated by designing a hierarchically interactive nano-network that is composed of elastic polymer nano-fibers and multi-level silver nano-wires (AgNWs). The elastic polymer nano-fibers act as a continuous scaffold, and multi-level AgNWs embedded in the nano-fibers form branched conductive pathways. This structure enables high conductivity of the SEE at 4800 S cm-1 (at a significantly low AgNW content of 1.59 vt%), with high stretchability and excellent durability. For example, the SEE remained conductive even at a high strain of 500%, and it also maintained its initial resistance even after 30 000 cycles of strain at 50% or being washed with water for 100 000 cycles. The SEE was prepared by a facile in situ nonequilibrium fabrication process, and can easily be produced into an elastic circuit on a large scale, which provides a foundation for integrated and multifunctional electronic skins. The SEE possesses superior mechanical conformability and permeability of gas and liquid, and therefore, it was successfully applied in measuring electrocardiogram signals and thermal therapy, and exhibited highly robust and comfortable performances even while being washed with water or undergoing complex deformations.

Small-Sized, Lightweight, and Flexible Triboelectric Nanogenerator Enhanced by PTFE/PDMS Nanocomposite Electret.

The rapid development of flexible and wearable electronics calls for a sustainable solution of the power supply. In recent years, the energy-harvesting triboelectric nanogenerator (TENG) has attracted increasing attentions due to its sustainability, flexibility, and versatility. However, achieving both high electric output and flexibility at the same time remains to be a challenge. In this work, we reported a corona charging enhanced flexible triboelectric nanogenerator (EF-TENG) to harvest mechanical energy from human motions. The EF-TENG relied on the repeated contacts between a poly(tetrafluoroethylene)/poly(dimethylsiloxane) nanocomposite electret and a nanofibers/AgNWs electrode on arrayed silicone pyramids. When the EF-TENG (3.5 × 3.5 cm2) was pressed, the open-circuit voltage ( Voc), the short-circuit current ( Isc), and the power density could reach 275 V, 9.5 µA, and 802.31 mW/m2, respectively. The Voc of the EF-TENG was improved by 244% compared to the device of which the electret was not corona charged. Major factors that affected the electric output of the EF-TENG were discussed, including the height of the pyramids, the configuration of the pyramids array, and the properties of the electret nanocomposite. The EF-TENG only had an overall thickness of 1.3 mm and a weight of 1.7 g, making it especially suitable to be attached onto human body for harvesting mechanical energy from biomechanical motions.

Flexible Porous Polydimethylsiloxane/Lead Zirconate Titanate-Based Nanogenerator Enabled by the Dual Effect of Ferroelectricity and Piezoelectricity.

Flexible piezoelectric nanogenerators have drawn considerable attention for their wide applications in harvesting ambient mechanical energy. Here, we report a flexible porous nanogenerator (FPNG) based on the dual effect of ferroelectricity and piezoelectricity. The electric output originated from the combination of the above two effects can be constructively added up, resulting in an enhancement of the electric output. With dimensions of 2 × 2 × 0.3 cm3, the FPNG can generate an open-circuit voltage ( Voc) of 29 V and a short-circuit current ( Isc) of 116 nA under a compressive force of 30 N. Besides, the FPNG is applicable to other forms of mechanical stimuli, including twisting and bending. Harvesting energy from a rowing bicycle tire is demonstrated in this report. This work provides a new route to promoting the electric output of piezoelectric nanogenerators.

Highly Robust, Transparent, and Breathable Epidermal Electrode.

Recently emerged electronic skins with applications in on-body sensing and human-machine interfaces call for the development of high-performance skin-like electrodes. In this work, we report a highly robust, transparent, and breathable epidermal electrode composed of a scaffold-reinforced conductive nanonetwork (SRCN). Solution-dispersed Ag nanowires, through facile vacuum filtration, are embedded into a scaffold made of polyamide nanofibers. Optical transmittance of 84.9% at 550 nm wavelength is achieved at a significantly low sheet resistance of 8.2 Ω sq-1. The resistance of the SRCN only slightly increases by less than 0.1% after being bent for 3000 cycles at the maximum curvature of 300 m-1 and by less than 1.5% after being dipped in saline solution for 2500 cycles. The excellent robustness is attributed to the reinforcement from the nanofiber-based scaffold as a backbone that maintains the connections among the Ag nanowires by undertaking most of the loaded stress. The SRCN not only forms tight and conformal bonding with the target surface but also allows the evaporation of perspiration, making it suitable as an epidermal electrode for long-time use. Furthermore, fine and clean-cut circuit patterns with a line width on the micrometer scale can be readily prepared, paving the way for fabricating sophisticated functional electronic skins.

Stretchable Porous Carbon Nanotube-Elastomer Hybrid Nanocomposite for Harvesting Mechanical Energy.

A stretchable porous nanocomposite (PNC) is reported based on a hybrid of a multiwalled carbon nanotubes network and a poly(dimethylsiloxane) matrix for harvesting energy from mechanical interactions. The deformation-enabled energy-generating process makes the PNC applicable to various mechanical interactions, including pressing, stretching, bending, and twisting. It can be potentially used as an energy solution for wearable electronics.

Triboelectric Charging at the Nanostructured Solid/Liquid Interface for Area-Scalable Wave Energy Conversion and Its Use in Corrosion Protection.

We report a flexible and area-scalable energy-harvesting technique for converting kinetic wave energy. Triboelectrification as a result of direct interaction between a dynamic wave and a large-area nanostructured solid surface produces an induced current among an array of electrodes. An integration method ensures that the induced current between any pair of electrodes can be constructively added up, which enables significant enhancement in output power and realizes area-scalable integration of electrode arrays. Internal and external factors that affect the electric output are comprehensively discussed. The produced electricity not only drives small electronics but also achieves effective impressed current cathodic protection. This type of thin-film-based device is a potentially practical solution of on-site sustained power supply at either coastal or off-shore sites wherever a dynamic wave is available. Potential applications include corrosion protection, pollution degradation, water desalination, and wireless sensing for marine surveillance.

Platinum nanoparticles on porphyrin functionalized graphene nanosheets as a superior catalyst for methanol electrooxidation.

A novel nanostructured catalyst of platinum nanoparticles supported on 5,10,15,20-tetrakis(1-methyl-4-pyridinio)porphyrin tetra(p-toluenesulfonate) (TMPyP) functionalized graphene (TMPyP-graphene) is synthesized by the hydrothermal polyol process. The as-synthesized nanocomposites are characterized by Fourier transform infrared (FTIR) spectroscopy, UV-vis absorption spectroscopy, Raman spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical tests. It has been found that Pt nanoparticles of ca. 3.4 nm are uniformly dispersed on the surface of TMPyP-graphene, and hold a high electrochemical active surface area (ECSA) of 126.2 m(2) g(-1). The results demonstrate that the Pt/TMPyP-graphene catalyst exhibits a much higher electrocatalytic activity and stability than the Pt/graphene and commercial Pt/C catalysts for methanol oxidation, which is of significant importance in improving the efficiency of Pt-based electrocatalysts for DMFCs applications.

Synthesis, structural characterization and luminescent properties of a series of Cu(I) complexes based on polyphosphine ligands.

A series of Cu(I) complexes with a [Cu(NN)(PP)](+) moiety, [Cu(phen)(pba)](BF(4)) (1a), [Cu(2)(phen)(2)(pbaa)](BF(4))(2) (2a), [Cu(2)(phen)(2)(pnaa)](BF(4))(2) (3a), [Cu(2)(phen)(2)(pbbaa)](BF(4))(2) (4a), [Cu(dmp)(pba)](BF(4)) (1b), [Cu(2)(dmp)(2)(pbaa)](BF(4))(2) (2b), [Cu(2)(dmp)(2)(pnaa)](BF(4))(2) (3b) and [Cu(2)(dmp)(2)(pbbaa)](BF(4))(2) (4b) (phen = 1,10-phenanthroline, dmp = 2,9-dimethyl-1,10-phenanthroline, pba = N,N-bis((diphenylphosphino)methyl)benzenamine, pbaa = N,N,N',N'-tetrakis((diphenylphosphino)methyl)benzene-1,4-diamine, pnaa = N,N,N',N'-tetrakis((diphenylphosphino)methyl)naphthalene-1,5-diamine and pbbaa = N,N,N',N'-tetrakis((diphenylphosphino)methyl)biphenyl-4,4'-diamine), were rationally designed and synthesized. These complexes were characterized by (1)H and (31)P NMR, electrospray mass spectrometry, elemental analysis and X-ray crystal structure analysis. Introduction of different central arene spacers (phenyl, naphthyl, biphenyl) into ligands, resulting in the size variation of these complexes, aims to tune the photophysical properties of the complexes. Each Cu(I) ion in these complexes adopts a distorted tetrahedral geometry constructed by the chelating diimine and phosphine groups. Intermolecular C-H···π and/or π···π interactions are involved in the solid states. The dmp-containing complex exhibits better emission relative to the corresponding phen complex due to the steric encumbrance of bulky alkyl groups. Furthermore, for complexes with identical diimine but different phosphine ligands, the tendency of increased emission lifetime as well as blue-shifted emission in the solid state follows with the decrease in size of complexes. Intermolecular C-H···π interactions have an influence on the final solid state photophysical properties through vibrationally relaxed non-radiative energy transfer in the excited state. Smaller-sized complexes show better photophysical properties due to less vibrationally relaxed behavior related to flexible C-H···π bonds. Nevertheless, the tendency for increased quantum yield and emission lifetime, as well as blue-shifted emission in dilute solution goes with the increase in size of complexes. The central arene ring (phenyl, naphthyl or biphenyl) has an influence on the final photophysical properties. The larger the π-conjugated extension of central arene ring is, the better the photophysical properties of complex are. The rigid and large-sized complex 3b, with a high quantum yield and long lifetime, is the best luminophore among these complexes.