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Effective host materials are required to improve the performance of phosphorescent organic light-emitting diodes (PhOLEDs). Herein, a series of triazine-dibenzofuran-based n-type host materials, DBT1–DBT4, was prepared by varying the substitution position of dibenzofuran. The photophysical, thermal, and electrochemical properties as well as the device performance of these materials were investigated to establish structure–property relationships. The results demonstrated that the substitution position of dibenzofuran significantly affects the chemical structure, resulting in differences in electrochemical and photophysical properties. All the developed materials were utilized in green top-emitting PhOLEDs as an n-type host material mixed with a p-type host (BPCz), and their electroluminescence (EL) properties were assessed by systematically analysing 18 devices. Among them, the green PhOLEDs using a mixed host of DBT4/BPCz (DBP4-III) displayed the best EL performance with a high current efficiency up to 131.98 cd A−1, an external quantum efficiency up to 30.90%, and a power efficiency up to 105.44 lm W−1 with a device lifetime (T95) of 180 h at 10 000 nits. These findings are expected to aid in the development of improved n-type host materials for highly efficient top-emitting PhOLEDs with long operational lifetimes.

We report on the fabrication of an interactive display system consisting of a stretchable array of electrochromic devices (ECDs) and temperature and strain sensors for visual display of skin temperature and wrist movement. The electrochromic device is prepared by coating poly(3-hexylthiophene) and tungsten trioxide as electrochromic materials on a flexible and transparent electrode of indium-tin-oxide-coated polyethylene terephthalate, and the subsequent assembly of the prepared electrodes using a gel-type electrolyte of Li-mixed 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide/poly(methyl methacrylate). The fabricated ECD exhibits three different colors due to the redox reactions of the electrochromic materials at the corresponding potentials: magenta, violet, and blue at −1.5 V, 0.5 V, and 1.5 V, respectively. By using patterned liquid metal Galinstan interconnections, a stretchable array of the ECDs is fabricated based on a strain relieving mechanism with an island-bridge design, resulting in mechanical stability to repeated stretching of up to 30%. A high-performance strain sensor is fabricated by embedding fragmentized graphene foams inside poly(demithylsiloxane) thin film, and a temperature sensor is prepared by embedding multi-walled carbon nanotubes/polyaniline composite in poly(vinyl alcohol) film. With the integrated system, the strain due to wrist bending and the skin temperature measured by the sensors are displayed as changes in the color pattern of the ECD array aided by an Arduino circuit. This work demonstrates the high potential of our system for application to wearable healthcare devices providing real-time visual display of varied bio-signals.

A highly-durable, highly-flexible transparent electrode (FTE) is developed by applying a composite made of a thin metal grid and a doped conducting polymer onto a colorless polyimide-coated NOA63 substrate. The proposed FTE exhibits a transparency of 90.7% at 550 nm including the substrate and a sheet resistance of 30.3 Ω/sq and can withstand both moderately high-temperature annealing (∼180 °C) and acidic solution (70 °C, pH 0.3) processes without performance degradation. The fabricated FTE yielded good mechanical stability under 10 000 cycles of bending deformations at a bending radius less than 1 mm without degradation of electrical conductivity. The high durability of the proposed FTE allows for the fabrication of flexible energy harvesting devices requiring harsh conditions, such as highly flexible perovskite solar cells (FPSCs) with a steady-state power conversion efficiency (PCE) of 12.7%. Notably, 93% of the original PCE is maintained after 2000 bending cycles at an extremely small bending radius of 1.5 mm. The FPSCs installed on curved surfaces of commercial devices drive them under various environments. The applicability of the proposed FTE is further confirmed via the fabrication of a flexible perovskite light-emitting diode. The proposed FTE demonstrates great potential for applications in the field of flexible optoelectronic devices.

Background and aims Renal dysfunction is a potent risk factor for cardiovascular diseases, including stroke. This study aimed to evaluate the impact of admission estimated glomerular filtration rate (eGFR) levels on short-term (1-month) and long-term (1-year) mortality in patients with acute ischemic stroke. Methods From the Taiwan Stroke Registry data, we classified ischemic stroke patients, identified from April 2006 to December 2015, into 5 groups by eGFR at admission: ≥ 90, 60–89, 30–59, 15–29, and Results Among 52,732 ischemic stroke patients, 1480 died within one month. The 1-month mortality rate was over 5-fold greater in patients with eGFR Conclusions After acute ischemic stroke, patients with reduced eGFR are at elevated risks of short-term and long-term deaths in a graded relationship.

In this report, high sensitivity pressure and temperature sensors are demonstrated based on a single common active material of poly(3-hexylthiophene-2,5-diyl) (P3HT)-coated elastic carbon foam (ECF) for bio-signal monitoring. A conductive microporous elastic foam is obtained via direct carbonization of a commercially available melamine foam at 700 °C and a subsequent dip coating with P3HT. The design incorporating interdigitated electrodes on the bottom of the P3HT-coated ECF is used to fabricate a high-performance pressure sensor with a high pressure sensitivity of 102.4 kPa−1 (

We investigated the impact of serum cholesterol levels on 30-day mortality after ischemic stroke in dialysis patients.From the Taiwan Stroke Registry data, we identified 46,770 ischemic stroke cases, including 1101 dialysis patients and 45,669 nondialysis patients from 2006 to 2013.Overall, the 30-day mortality was 1.46-fold greater in the dialysis group than in the nondialysis group (1.75 versus 1.20 per 1000 person-days). The mortality rates were 1.64, .62, 2.82, and 2.23 per 1000 person-days in dialysis patients with serum total cholesterol levels of 120 mg/dL, 120-159 mg/dL, 160-199 mg/dL, and ≥200 mg/dL, respectively. Compared to dialysis patients with serum total cholesterol levels of 120-159 mg/dL, the corresponding adjusted hazard ratios of mortality were 4.20 (95% confidence interval [CI] = 1.01-17.4), 8.06 (95% CI = 2.02-32.2), and 6.89 (95% CI = 1.59-29.8) for those with cholesterol levels of 120 mg/dL, 160-199 mg/dL, and ≥200 mg/dL, respectively.Dialysis patients with serum total cholesterol levels of ≥160 mg/dL or 120 mg/dL on admission are at an elevated hazard of 30-day mortality after ischemic stroke.

We report on the fabrication of a high performance flexible micro-supercapacitor (MSC) for powering a vertically integrated skin-attachable strain sensor on a gecko-inspired micro-structured adhesive. Combined utilization of the mixed manganese/vanadium (Mn/V) oxide grown on MWCNT electrode and the sulfone-based electrolyte, PC/SL/LiClO4/PMMA, enhances both the capacitance and operation voltage up to 2 V of MSC. Thus, the fabricated MSC exhibits excellent electrochemical performance with an areal capacitance of 11.8 mF cm−2 and an areal energy density of 6.58 µWh cm−2 at an areal power density of 200 µW cm−2. The MSC shows mechanical stability over 1000 repetitive bends at a bending radius of 3.7 mm. The strain sensor made of fragmentized graphene foam embedded in PDMS film provides a high gauge factor of 12.6 up to 50% strain to detect strains due to various bio-signals. Our gecko-inspired adhesive made of PDMS micropillars inked with a mixture of PDMS and Silbione to have spatula tips exhibits not only high adhesion property but also high durability over repeated cycles of attachment-detachment and negligible skin irritation. After vertical integration of the MSC, strain sensor, and the adhesive film, bio-signals such as an arterial pulse, swallowing, and frowning of the brow are successfully detected using energy stored in the MSC.

A series of double donor-acceptor organic dyes (C4 C12) have been synthesized to investigate the influence of the alkyl chain length between the two chromophores on the performance of dye sensitized solar cells (DSSCs). The chain length dependent performance was investigated further using the electrochemical impedance and stepped light induced transient measurement methods. Dye with longer alkyl chain (C6 C12) shows a broader and higher IPCE as well as photo-current density (Jsc) with an enhanced photovoltage (Voc) relative to the reference PTZ-S. In contrast, C4 with shorter alkyl chain presents a relatively low IPCE within the whole spectral region, along with low Jsc and Voc, which predominately arising from the short electron diffusion length with significant electron loss during charge transport. The higher Jsc and Voc obtained with the devices incorporating C10 and C12 dyes with long alkyl chain resulted in a higher conversion efficiencies of 4.02% and 4.03%, respectively, (3.14% for single donor-acceptor dye PTZ-S). Density functional theory simulations were also performed to examine the effect of the alkyl chain length on electrochemical and optical properties of the dyes. Adsorption studies of the dyes on TiO 2 clusters were carried out to explain the variation in Jsc with the alkyl chain length.

The effect of chenodeoxycholic acid (CDCA) used as the coadsorbent with a symmetrical squaraine (SSQ) sensitizer on TiO2-based solar cells was investigated, and it was found that the coadsorbent re...

An organic sensitizer with a multi-anchoring system is a versatile methodology for enhancing the stability and conversion efficiency of dye-sensitized solar cells (DSSCs). Triphenylamine dyes (TPA3T1A ∼ 3A) containing different numbers of anchoring groups are synthesized to determine the correlation between the number of anchoring groups and photovoltaic properties as photosensitizers for DSSCs. The adsorption properties of the dyes on TiO2 electrode were examined by ATR-FT-IR, which show that a mono-anchoring TPA3T1A system adsorbs in monodentate ester-type mode, and the three carboxylic acids in TPA3T3A adsorbs in bidentate bridging mode. The multi-anchoring dye exhibits strong electronic coupling with TiO2, providing an efficient charge injection rate. Moreover, they increased the electron lifetime significantly by suppressing the charge recombination probability. This synergistic effect enables the fabrication of efficient photovoltaic devices. Furthermore, enhanced long-term stability is also observed in the DSSCs containing a tri-anchoring system compared to the mono- and bi-anchoring systems.

CH3NH3PbX3 (MAPbX3) perovskites have attracted considerable attention as absorber materials for solar light harvesting, reaching solar to power conversion efficiencies above 20%. In spite of the rapid evolution of the efficiencies, the understanding of basic properties of these semiconductors is still ongoing. One phenomenon with so far unclear origin is the so-called hysteresis in the current–voltage characteristics of these solar cells. Here we investigate the origin of this phenomenon with a combined experimental and computational approach. Experimentally the activation energy for the hysteretic process is determined and compared with the computational results. First-principles simulations show that the timescale for MA+ rotation excludes a MA-related ferroelectric effect as possible origin for the observed hysteresis. On the other hand, the computationally determined activation energies for halide ion (vacancy) migration are in excellent agreement with the experimentally determined values, suggesting that the migration of this species causes the observed hysteretic behaviour of these solar cells., The origin of hysteresis remains an open question in lead-halide perovskite solar cells. Here, Meloni et al. investigate the causes of hysteresis using an experimental and computational approach, finding that the observed hysteresis is due to halide ion-vacancy movement in the perovskite.

We report on the fabrication of a fractal-designed transparent and stretchable (TS) microsupercapacitor (MSC) as a skin-attachable energy storage device for driving an integrated strain sensor (SS). The MSC is designed to have a fractal structure with long and narrow patterns to ensure high transparency and stretchability. MnO2/Carbon nanotubes (CNTs) and 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide/poly(methyl methacrylate) ([BMIM][TFSI]/PMMA) are used as electrodes and a stretchable electrolyte for the MSC, respectively. The fabricated MSC exhibits high transparency of 79% and an areal capacitance of 12.6 mF cm−2 at a current density of 5 mA cm−2. The TS MSC shows excellent mechanical stability in that it can maintain stable electrochemical performance even after 2000 repeated stretching cycles up to 30%. The TS SS is facilely prepared via spray coating of Ag nanowires (NWs) and subsequent curing of PDMS, where the transparency and the electrical resistance are controlled by adjusting the deposited volume of Ag NWs. Wrist bending and a wrist pulse are detected by the SS driven with the stored energy of the MSC. This work demonstrates the possible application of our TS MSC to future skin-attachable electronics as an integrated energy storage device.

Here, we report on a highly conductive, stretchable, and transparent electrode of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) fabricated via modification with triblock copolymer, poly(ethylene glycol)–block–poly(propylene glycol)–block–poly(ethylene glycol) (PEO20–PPO70–PEO20, Pluronic P123), and post-treatment with sulfuric acid. The fabricated electrode exhibits high transparency (89%), high electrical conductivity (∼1700 S/cm), and minimal change in resistance (∼4%) under repetitive stretch–release cycles at 40% tensile strain after stabilization. P123 acts as a secondary dopant and plasticizer, resulting in enhanced electrical conductivity and stretchability of PEDOT:PSS. Furthermore, after sulfuric acid post-treatment, P123 helps the electrode to maintain its stretchability. A successful demonstration of the stretchable interconnection was shown by stretching the P123-modified PEDOT:PSS electrodes, which were connected with light-emitting diodes (LEDs) in series. Finally, a st...

Hybrid organic–inorganic metal perovskites have emerged as highly promising materials for solar energy conversion. However, key questions regarding the working principles of perovskite solar cells remain to be answered in order to improve the design of such devices. In the present study, we have investigated the influence of excess excitation energy on the initial photo-products generated from FTO/meso-TiO2/CH3NH3PbI3 samples. We find that upon resonant excitation at the band edge, part of the formation of free charges passes via an excitonic state that dissociates on the sub-picosecond time scale. An exciton binding energy of

A stretchable polyaniline nanofiber temperature sensor array with an active matrix consisting of single-walled carbon nanotube thin-film transistors is demonstrated. The integrated temperature sensor array gives mechanical stability under biaxial stretching of 30%, and the resultant spatial temperature mapping does not show any mechanical or electrical degradation.

Organometal halide perovskites have emerged as promising next-generation solar cell technologies presenting outstanding efficiencies. However, many questions concerning their working principles remain to be answered. Here, we present a detailed study of hole transfer dynamics into polymeric hole transporting materials (HTMs), poly(triarylamine) (PTAA), poly(3-hexylthiophee-2,5-diyl (P3HT), and poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7-(2,1,3-benzothiadiazole) (PCPDTBT). The hole transfer dynamics are shown to occur on a time scale of thousands of picoseconds, being orders of magnitude slower compared to hole transfer involving commonly used Spiro-OMeTAD as HTM.

The effect of the presence of unreacted PbI2 on the perovskite solar cells efficiency is reported. N,N-Dimethylformamide vapor treatment is introduced to study the influence of complete conversion to a power conversion efficiency of the device. It is discovered that the optimized morphology of the PbI2 under layer is essential to form a dense perovskite layer preventing recombination by direct contact between TiO2 and a hole transporting layer, and to increase the charge collection efficiency. The present findings provide an insight into the morphology and growth mechanism of perovskite layer, the correlation between the device performance, and the film deposition process.

A flexible liquid metal loudspeaker (LML) is demonstrated consisting of a gallium-based eutectic liquid metal (Galinstan) and basic aqueous electrolyte (NaOH(aq) ). The LML is driven by liquid metal motion induced by the electrochemically controlled interfacial tension of the Galinstan in NaOH(aq) electrolyte under an applied alternating current (AC) voltage. The fabricated LML produces sound waves in the human audible frequency band with a sound pressure level of ≈40-50 dB at 1 cm from the device and exhibits mechanical stability under bending deformation with a bending radius of 3 mm. Various sounds can be generated with the LML from a single tone to piano notes and human voices. To understand the underlying mechanism of sound generation by the LML, motion analyses, sound measurements, and electrical characterization are conducted at various frequencies. For the first time, this work suggests a new type of liquid metal-based electrochemically driven sound generator in the field of flexible acoustic devices that can be applied to future wearable electronics.

The Al2 O3 passivation layer is beneficial for mesoporous TiO2 -based perovskite solar cells when it is deposited selectively on the compact TiO2 surface. Such a passivation layer suppressing surface recombination can be formed by thermal decomposition of the perovskite layer during post-annealing.

A foldable array of patterned graphene/ZnO nanoparticle UV sensor and asymmetric micro-supercapacitors (AMSCs) integrated on a paper substrate with patterned liquid metal interconnections is reported. The resistor type UV sensor based on graphene/ZnO nanoparticles is patterned to be driven by the stored energy of the integrated AMSCs. The AMSC consists of MnO2 nanoball deposited multiwalled carbon nanotubes (MWNTs) and V2O5 wrapped MWNTs as positive and negative electrodes, respectively. As an electrolyte, propylene carbonate-poly(methyl methacrylate)-LiClO4, an organic solvent-based gel, is used. The UV sensor and AMSCs can be easily integrated on a liquid metal, Galinstan, patterned, waterproof mineral paper and show a mechanically stable UV sensing, regardless of repetitive folding cycles. This work demonstrates a novel foldable nanomaterial based sensor system driven by integrated energy storage devices, applicable to future wearable and portable electronics.