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Background: The current guidelines for managing screen‐detected pulmonary nodules offer rule‐based recommendations for immediate diagnostic work‐up or follow‐up at intervals of 3, 6, or 12 months. Customized visit plans are lacking. Purpose: To develop individualized screening schedules using reinforcement learning (RL) and evaluate the effectiveness of RL‐based policy models. Methods: Using a nested case–control design, we retrospectively identified 308 patients with cancer who had positive screening results in at least two screening rounds in the National Lung Screening Trial. We established a control group that included cancer‐free patients with nodules, matched (1:1) according to the year of cancer diagnosis. By generating 10,164 sequence decision episodes, we trained RL‐based policy models, incorporating nodule diameter alone, combined with nodule appearance (attenuation and margin) and/or patient information (age, sex, smoking status, pack‐years, and family history). We calculated rates of misdiagnosis, missed diagnosis, and delayed diagnosis, and compared the performance of RL‐based policy models with rule‐based follow‐up protocols (National Comprehensive Cancer Network guideline; China Guideline for the Screening and Early Detection of Lung Cancer). Results: We identified significant interactions between certain variables (e.g., nodule shape and patient smoking pack‐years, beyond those considered in guideline protocols) and the selection of follow‐up testing intervals, thereby impacting the quality of the decision sequence. In validation, one RL‐based policy model achieved rates of 12.3% for misdiagnosis, 9.7% for missed diagnosis, and 11.7% for delayed diagnosis. Compared with the two rule‐based protocols, the three best‐performing RL‐based policy models consistently demonstrated optimal performance for specific patient subgroups based on disease characteristics (benign or malignant), nodule phenotypes (size, shape, and attenuation), and individual attributes. Conclusions: This study highlights the potential of using an RL‐based approach that is both clinically interpretable and performance‐robust to develop personalized lung cancer screening schedules. Our findings present opportunities for enhancing the current cancer screening system. [ABSTRACT FROM AUTHOR]

With the advent of cancer immunotherapy, some special features including delayed treatment effect, cure rate, diminishing treatment effect and crossing survival are often observed in survival analysis. They violate the proportional hazard model assumption and pose a unique challenge for the conventional trial design and analysis strategies. Many methods like cure rate model have been developed based on mixture model to incorporate some of these features. In this work, we extend the mixture model to deal with multiple non‐proportional patterns and develop its geometric average hazard ratio (gAHR) to quantify the treatment effect. We further derive a sample size and power formula based on the non‐centrality parameter of the log‐rank test and conduct a thorough analysis of the impact of each parameter on performance. Simulation studies showed a clear advantage of our new method over the proportional hazard based calculation across different non‐proportional hazard scenarios. Moreover, the mixture modeling of two real trials demonstrates how to use the prior information on the survival distribution among patients with different biomarker and early efficacy results in practice. By comparison with a simulation‐based design, the new method provided a more efficient way to compute the power and sample size with high accuracy of estimation. Overall, both theoretical derivation and empirical studies demonstrate the promise of the proposed method in powering future innovative trial designs. [ABSTRACT FROM AUTHOR]

Potassium‐ion batteries (KIBs) are promising energy storage devices owing to the close redox potential of potassium (K) to lithium and rich abundance of K resource, thus promoting the exploration of efficient cathode materials for K‐ions storage. Fe‐based Prussian blue analogues (KFeHCF) are promising cathode materials for KIBs due to their combined advantages in low cost and high energy density. However, the rapid capacity decay induced by unstable cathode electrolyte interphase (CEI) and dissolution of transition metal ions leads to limited lifespans (e.g., hundreds of cycles) of K∥KFeHCF batteries. Incorporating additives into electrolytes is an economical and effective way to construct robust CEI for high‐performance KIBs. Herein, a multifunctional electrolyte additive, potassium selenocyanate (KSeCN), is introduced to effectively construct stable, homogeneous and conductive CEI films, which leads to the inhibition of Fe dissolution and stabilization of KFeHCF structure during cycling. With 0.5 wt% of KSeCN in conventional carbonated electrolyte, the K∥KFeHCF battery exhibits promoted cycling performance with a capacity retention rate of 87% after 500 cycles at 4.5 V cutoff voltage. This finding provides a new paradigm for developing and designing potassium‐ion battery electrolytes. [ABSTRACT FROM AUTHOR]

MXene‐based supercapacitors are promising electrochemical energy‐storage devices due to their ultrahigh volumetric capacitance, high‐power characteristics, and excellent cyclability. However, they suffer from severe self‐discharging behavior while the underlying self‐discharging mechanism is still unclear. Here, the self‐discharge behavior of MXene‐based supercapacitors from surface electronic structure of MXenes is disclosed, and a novel method to mitigate it is proposed. A superficial engineering strategy based on bio‐thermal treatment is developed to effectively tailor surface electronic structure of Ti3C2Tx MXenes by eliminating hydroxyl terminations. With the evolution of surface electronic structure, as revealed by Kelvin probe force microscope and synchrotron radiation X‐ray absorption fine structure analysis, MXene‐based supercapacitors with common aqueous electrolytes show >20% decline in self‐discharge rate. This decline mechanism originates from the increased work function that induces higher zero‐charge potential after the removal of hydroxyl groups in MXenes. Meanwhile, the strengthened surface dipole leads to higher surface free energy between MXene and electrolytes. These two positive effects endow MXenes with weaker self‐discharge kinetics. Specifically, the activation‐controlled self‐discharge process is greatly suppressed. Illuminating the relevance between electronic structure and self‐discharge accompanying superficial engineering suppression strategy can guide to development of high‐performance energy storage devices. [ABSTRACT FROM AUTHOR]

Accumulation of liquids near the wellbore in gas reservoirs can result in what is known as liquid banking, causing loss of gas and liquid production. One of the techniques that can be used to mitigate liquid banking is changing the rock wettability from liquid wetting to neutral wetting, allowing the gas to carry the liquid out of the pore space. Double‐functionalized wettability altering silica (SiO2) nanoparticles (NPs) were developed. The synthesized NPs were functionalized with both fluoro‐silane (F‐SiO2 NPs) and a charged functional group to enable coupling of the NPs to the substrate. Surfaces treated with F‐SiO2 NPs functionalized with coupling functional group showed superior wear and corrosion resistance in high salinity water compared to single‐functionalized F‐SiO2 NPs. By functionalizing 125 nm SiO2 NPs first with polyethylenimine (PEI‐) or N‐(2‐Aminoethyl)‐3‐aminopropyltrimethoxysilane (DAMO‐) l group followed by fluorination, a water contact angle of 120°and decane contact angle of 70° was achieved. Core flow testing performed under realistic reservoir conditions of pressure and temperature showed that F‐SiO2 NPs coated with PEI achieved a 58% improvement in gas and liquid relative permeability, indicating improvement in the surface repellency to liquids and reduction of the trapped liquid phases inside the pore space of the rocks. The developed double‐functionalized NPs achieved similar performance to the commercially used fluorinated surfactants but using less treatment volume. In addition, these double‐functionalized NPs enable one‐step treatment in the field, which results in simpler operations, shorter treatment time, and better treatment economics. [ABSTRACT FROM AUTHOR]

This article discusses the development of thermally activated delayed fluorescent (TADF) materials for use in organic light-emitting diodes (OLEDs). The authors designed and synthesized two molecules, CQPh and CQPy, based on carbazole donors and benzopyrimidine acceptors. The photoluminescence spectra of these molecules were measured, and it was found that CQPh showed better device performance in red OLEDs, achieving a maximum external quantum efficiency (EQE) of 50.19%. The results suggest that CQPh is an excellent host for high-performance red electroluminescent devices. [Extracted from the article]

This document, titled "Intermolecular Charge Transfer for High-Performance Organic Light-Emitting Diodes," discusses the use of thermally activated delayed fluorescence (TADF) materials in organic light-emitting diodes (OLEDs) to achieve high-performance devices. Specifically, the authors designed and synthesized two new molecules, CzPh-1 and CzPh-2, which were found to form deep-blue exciple emission with a triazine-containing molecule, CzTrz, through effective intermolecular charge transfer. The photoluminescence spectra and time-resolved photoluminescence studies demonstrated the TADF characteristics of these materials. The authors acknowledge the support from the National Natural Science Foundation of China and the China Postdoctoral Science Foundation. [Extracted from the article]

A facile method to prepare flexible n‐type Ag2Se/Se/polypyrrole (PPy) composite films is developed. First, Ag2Se nanostructures (NSs) are wet chemically synthesized; PPy is then in situ polymerized at the surface of the Ag2Se NSs; and finally, the Ag2Se/Se/PPy composite film on a porous nylon membrane is fabricated by a vacuum‐assisted filtration process followed by hot pressing. An optimal composite film shows an exceptionally high power factor of ≈2240 µW m−1 K−2 at 300 K, mainly because of the synergistic effect between well‐developed crystalline Ag2Se grains and a small amount of Se and PPy. The film also possesses outstanding flexibility (only about 6.5% decrease in electrical conductivity after 1000 times bending along a rod with a radius of 4 mm). Moreover, a flexible thermoelectric generator composed of six legs of the film outputs a voltage of 21.2 mV and a maximum power of 4.04 µW (corresponding power density of 37.6 W m−2) at a temperature difference of 34.1 K, verifying exceptionally high thermoelectric properties. This work shows the promise of the as‐prepared composite film for practical applications in wearable devices and will surely promote the research and development of flexible TE generators. [ABSTRACT FROM AUTHOR]

In this study, a novel Co3O4/Co(OH)2 heterostructure is obtained via electrodeposition on nickel (Ni) foam, forming sandwich‐like structure and freestanding electrode. The outer Co(OH)2 with layered structure can provide sufficient absorption sites and enable facile ion intercalation, meanwhile the presence of a conductive and robust interfacial Co3O4 layer between Ni foam and Co(OH)2 is found effectively minimizes the charge transfer resistance and stabilizes the interface, thus improving the electrode's rate and cycling performance with high capacity preserved synergistically. Furthermore, the structural evolution of Co(OH)2 and Co3O4 upon cycling are elucidated systematically using a series of in situ and ex situ techniques. The Co(OH)2 is found irreversibly changed to CoOOH upon first charge, which is then reversibly converted to CoO2 during the subsequent charge–discharge cycles. The Co3O4 exhibits negligible phase changes of the bulk upon cycling, indicating its good structural integrity that contributes to the significantly improved cyclability. In general, this work not only offers an ease and effective approach to optimize the charge storage properties of Co3O4/Co(OH)2 heterostructure via interfacial layer control, but also provides valuable insights in understanding their charge storage mechanisms, which may inspire the development of more heterostructures or extend to other applications. [ABSTRACT FROM AUTHOR]

Spinel cobaltites are widely presented as promising pseudocapacitive materials, however, a fundamental understanding of their structure–property relationship at an atomic level remains vague. Herein, their geometrical‐site‐dependent charge storage capability is investigated by substituting Co with inactive Zn and redox‐active Mn. Experimental and theoretical analyses reveal that redox‐active cations in octahedral sites contribute to enhanced capacitance, intrinsically determined by the covalency competition between tetrahedral and octahedral sites. The Zn2+ incorporation leads to increased occupancy of Co in octahedral sites and 2.9× increased capacitance at 1 A g−1 current density, whereas the substituted Mn cations mainly sit in octahedral sites which can react with OH− upon cycling and separate on the spinel surface to reconstruct into δ‐MnO2 nanosheets, leading to 4× increased capacitance at 1 A g−1 current density with a detected K+ ion intercalation. Thus, the exposure of redox‐active cations in octahedral sites and their intrinsic properties are influential in determining spinel oxides' pseudocapacitive properties. This work provides a general principle to optimize the pseudocapacitive properties of spinel cobaltites by deliberately selecting cations for substitution and controlling their distribution in octahedral/tetrahedral sites. It also offers a fundamental understanding of geometrical‐site‐dependent activity, and can effectively guide the development of spinel oxides for enhanced pseudocapacitance. [ABSTRACT FROM AUTHOR]

High power and good stability enable supercapacitors to work efficiently at high temperatures. However, the high‐temperature‐induced excessive ion transfer of the electrolyte would lead to severe self‐discharge behavior, which has often been overlooked but can be highly detrimental. In this study, solid electrolytes consisting of poly(ethylene oxide) (PEO), bentonite clay, and ionic liquids (IL)‐PEO‐clay@[EMIM][BF4] (PCE), PEO‐clay@[BMIM][BF4] (PCB), and PEO‐clay@[HMIM][BF4] (PCH) lead to dramatic decreases in self‐discharge when used in all‐solid‐state supercapacitors at high temperature of 70 °C, which correlate with chain elongation (i. e., [EMIM+]<[BMIM+]<[HMIM+]). Benefiting from both cation adsorption and high‐temperature stabilization by bentonite clay, PCH‐based supercapacitors (IL=[HMIM][BF4]) deliver an extremely low self‐discharge rate, with only a 30.7 % voltage drop over 10 h at 70 °C (44.5 % for 38 h), which is much lower than that of traditional liquid supercapacitors (63.7 % drop over 10 h at 70 °C). This improvement in high‐temperature self‐discharge behavior is found to be from the decrease in diffusion‐controlled faradaic process. Based on the longer‐chain [HMIM+], soft‐packaged supercapacitors exhibit a low self‐discharge rate and work consistently at 70 °C. This chain‐elongation strategy provides a new possibility for the suppression of self‐discharge behavior in supercapacitors and further aids long‐term energy storage by supercapacitors at high temperatures. [ABSTRACT FROM AUTHOR]

Background and Objective: Parathyroid carcinoma (PC) is a rare malignant neoplasm with a relatively poor prognosis. The loss of parafibromin expression or the presence of CDC73 mutation has been found to be remarkably associated with malignancy in parathyroid tumours. However, the prognostic role of them in PC has not yet been shown due to sampling limitations. We conducted a systematic review and meta‐analysis based on individual patient data to clarify the performance of parafibromin immunohistochemical staining and CDC73 gene sequencing in predicting outcomes for patients PC. Methods: Published studies from PubMed/MEDLINE, EMBASE, Cochrane and Scopus Databases were searched using the terms 'parafibromin', 'CDC73', 'HRPT2' and 'parathyroid' to identify eligible studies. From the included studies, the survival data of patients with PC were extracted, and a Cox proportional hazards model was used to assess hazard ratio (HR) for disease‐free survival (DFS) and overall survival (OS). Results: A total of 193 patients from 9 studies were included in this survival analysis. Negative immunohistochemical staining of parafibromin was shown to be a risk factor for recurrence/metastasis (HR 2.73, P =.002) and death (HR 2.54, P =.004). Patient age ≥ 50 years was significantly related to lower OS (HR 2.37, P =.004) but not to DFS. CDC73 mutation was not statistically related to DFS or OS. Conclusions: Negative parafibromin staining indicated a higher risk of recurrence/metastasis and mortality. The immunohistochemical staining of parafibromin seems to be more promising in predicting outcomes for patients with PC than the sequencing of CDC73. [ABSTRACT FROM AUTHOR]

Background and Objectives: A health industry standard recommending restrictive transfusion is to be in effect in China in April 2019. We aim to explore its potential economic and clinical impacts among surgical patients. Materials and Methods: A decision tree model was applied to compare cost‐effectiveness of current routine transfusion in China, a restrictive (transfusion at Hb < 8 g/dl or ischaemic symptoms) and a liberal (transfusion at Hb < 10 g/dl) strategy. Parameters were estimated from empirical data of 25 227 surgical inpatients aged ≥30 years in a multicenter study and supplemented by meta‐analysis when necessary. Results are shown for cardio‐cerebral‐vascular (CCV) surgery and non‐CCV (orthopaedics, general, thoracic) surgery separately. Results: Per 10 000 patients in routine, restrictive, liberal transfusion scenarios, total spending (transfusion and length of stay related) was 7·67, 7·58 and 9·39 million CNY (1 CNY × 0.157 = 1 US dollar) for CCV surgery and 6·35, 6·70 and 8·09 million CNY for non‐CCV surgery; infectious and severe complications numbered 354, 290, and 290 (CCV) and 315, 286, and 330 (non‐CCV), respectively. Acceptability curves showed high probabilities for restrictive strategy to be cost‐effective across a wide range of willingness‐to‐pay values. Such findings were mostly consistent in sensitivity and subgroup analyses except for patients with cardiac problems. Conclusion: We showed strong rationale, succeeding previous findings only in cardiac or joint procedures, to comply with the new standard as restrictive transfusion has high potential to save blood, secure safety, and is cost‐effective for a wide spectrum of surgical patients. Experiences should be further summarized to pave the way towards individualized transfusion. [ABSTRACT FROM AUTHOR]

The AC impedance of SrTiO3, Ca0.9Sr0.1TiO3, Ca0.7Sm0.2TiO3, and Ca0.7Sm0.3Ti0.7Al0.3O3 microwave dielectric ceramics with perovskite structures has been analyzed. The impedance spectroscopy results reveal the electrical properties of this series of samples vary significantly with the ceramic microstructure and electrical homogeneity. The εr values of grains for SrTiO3 and Ca0.9Sr0.1TiO3 ceramics are 193.8 and 138.1, respectively, confirming that dielectric response of the high‐εr microwave ceramics is contributed to the grains, at microwave frequencies. Impedance spectroscopy of Ca0.7Sm0.2TiO3 ceramic illustrates that electrical heterogeneous microstructures include interior grains and grain shells. The secondary phase existing in Ca0.7Sm0.2TiO3 ceramic causes deviation in bulk permittivity, resulting in a higher εr ~ 148 of grains than εr ~ 112 of bulk permittivity, measured at microwave frequencies. Grain and grain‐boundary impedance of Ca0.7Sm0.3Ti0.7Al0.3O3 ceramic cannot be separated completely. The permittivities of grains and grain boundaries in Ca0.7Sm0.3Ti0.7Al0.3O3 ceramic are εg ~ 17.8 and εgb ~ 20.8, and the combination of them is close to εr ~ 40 at microwave frequencies. The LogI−LogU curves of the ceramic system indicate that the conducting mechanism of grains and grain boundaries follows ohmic behavior. [ABSTRACT FROM AUTHOR]

In this paper, we successfully demonstrated high color rendering index (CRI) and color stable white organic light-emitting diodes (WOLEDs) based on a hole-type single-host double emissive layer (EML) structure. By combining the yellow phosphorescent emission with the blue monomer and red excimer emission of platinum [1,3-difluoro-4,6-di(2-pyridinyl)benzene]chloride (Pt-4), the devices exhibited a maximum CRI of 93, which was attributed to the perfect spectrum complement and the relative intensity adjustment of each emission peak. Meanwhile, the WOLEDs were very stable and showed a slight color coordinate shift of (±0.007, ±0.004) over a wide range of driving voltages from 4 to 10 V. The use of the double EML structure effectively confines the exciton generation zone in the Pt-4 EML, thus, the white-light emission comes from the energy transfer from host to Pt-4 and then to yellow phosphor, which is less affected by the driving conditions. [ABSTRACT FROM AUTHOR]

High efficiency performance and color rendering index (CRI) are two main requirements for the applications of white organic light-emitting diodes (WOLEDs). We report successful fabrication of efficient and high-color-rendering phosphorescent WOLED by employing ultra-thin red emitter - spacer layer - ultra-thin green emitter architecture. By fine-tuning the thicknesses of emitting layers and spacer layer, we have obtained WOLED with a high CRI of 80 and high luminance efficiency (LE) of 29.2 cd A−1 which only rolls off to 22.8 cd A−1 at 1000 cd m−2. A typical WOLED for comparison exhibits a CRI below 40 and maximum LE of 15.8 cd A−1 which decreases to 11.4 cd A−1 at 1000 cd m−2. The superiority of ultra-thin device compared with typical device demonstrates utilizing ultra-thin emitting layer is a promising technique to achieve high performance organic light-emitting diode (OLED). [ABSTRACT FROM AUTHOR]

A great number of obsolete larval neurons in the Drosophila central nervous system are eliminated by developmentally programmed cell death (PCD) during early metamorphosis. To elucidate the mechanisms of neuronal PCD occurring during this period, we undertook genetic dissection of seven currently known Drosophila caspases in the PCD of a group of interneurons (vCrz) that produce corazonin (Crz) neuropeptide in the ventral nerve cord. The molecular death program in the vCrz neurons initiates within 1 hour after pupariation, as demonstrated by the cytological signs of cell death and caspase activation. PCD was significantly suppressed in dronc-null mutants, but not in null mutants of either dredd or strica. A double mutation lacking both dronc and strica impaired PCD phenotype more severely than did a dronc mutation alone, but comparably to a triple dredd/strica/dronc mutation, indicating that dronc is a main initiator caspase, while strica plays a minor role that overlaps with dronc's. As for effector caspases, vCrz PCD requires both ice and dcp-1 functions, as they work cooperatively for a timely removal of the vCrz neurons. Interestingly, the activation of the Ice and Dcp-1 is not solely dependent on Dronc and Strica, implying an alternative pathway to activate the effectors. Two remaining effector caspase genes, decay and damm, found no apparent functions in the neuronal PCD, at least during early metamorphosis. Overall, our work revealed that vCrz PCD utilizes dronc, strica, dcp-1, and ice wherein the activation of Ice and Dcp-1 requires a novel pathway in addition to the initiator caspases. J. Comp. Neurol. 519:34-48, 2011. © 2010 Wiley-Liss, Inc. [ABSTRACT FROM AUTHOR]

The turn-on voltage of devices are 3.9V, it is worth noting that the efficiency of devices is very low when it is turned on. Wavelength (nm) (b) EQE (%) Luminance (cd/m 2) device 1 device 2 Fig. Energy level of devices 2 4 6 8 10 12 14 16 18 20 0 10 20 30 40 50 60 70 80 90 device 1 device 2 Voltage (V) Current Density (mA/cm 2) 10 0 10 1 10 2 10 3 10 4 (a) Luminance(cd/m 2) 10 0 10 1 10 2 10 3 10 4 10 -2 10 -1 10 0 10 1 10 2 400 500 600 700 0.0 0.2 0.4 0.6 0.8 1.0 Normalized Intensity (a.u.). [Extracted from the article]

A co-host emissive layer that consists of mixed mCP and PPO2 was obtained to achieve the current efficiency and power efficiency of 12.9 cd/A and 9.6 lm/W as a blue OLED with the CIE coordinates of (0.16, 0.26). Current and power efficiencies curves (Insert EL spectra) of blue OLEDs 0.01 0.1 1 10 0 4 8 12 16 20 24 28 32 Current efficiency Power efficiency Current density/mA- cm -2 Current efficiency/cd- A -1 0 5 10 15 20 25 400 450 500 550 600 650 700 750 0.0 0.2 0.4 0.6 0.8 1.0 1.2 EL intensity/a.u. Wavelength/nm 100 cd- m -2 500 cd- m -2 1000 cd- m -2 Current efficiency Power efficiency Current density/mA- cm -2 Current efficiency/cd- A -1 0 5 10 15 20 Power efficiency/lm- W -1 Fig. [Extracted from the article]

Thermoelectric (TE) fibers are more suitable than films for portable or wearable devices. Herein, 2–3 nm thick poly (3,4‐ethylenedioxythiophene): poly (styrenesulfonate) (PEDOT:PSS) layer‐coated tellurium nanowires (PC‐Te NWs) are in situ prepared by a hydrothermal method. Then a series of PEDOT: PSS/PC‐Te NWs composite fibers are prepared by wet spinning and post‐treatment. The nanolayer prevents the agglomeration of the Te NWs and makes the NWs and PEDOT:PSS matrix have good compatibility, which results in the PC‐Te NWs content to a high value of 70 wt% and the fibers still with flexibility. The high aspect ratio of the PC‐Te NWs and the stress from the inner wall of the needle during spinning make the NWs ordered align along the composite fiber. Due to the large content and orientational arrangement of the PC‐Te NWs, as well as effective post‐treatment, an optimized composite fiber shows a power factor of 385.4 µW m−1 K−2 at 300 K, which is ≈4.9 times as high as the highest value of previously reported PEDOT:PSS/Te NWs‐based composite fibers. In addition, the composite fiber has good flexibility. The flexible TE generators assembled have excellent output performance. This work provides an effective strategy for the preparation of high‐performance flexible TE composite fibers. [ABSTRACT FROM AUTHOR]

Polymer dielectrics find applications in modern electronic and electrical technologies due to their low density, durability, high dielectric breakdown strength, and design flexibility. However, they are not reliable at high temperatures due to their low mechanical integrity and thermal stability. Herein, a self‐assembled dielectric nanocomposite is reported, which integrates 1D polyaramid nanofibers and 2D boron nitride nanosheets through a vacuum‐assisted layer‐by‐layer infiltration process. The resulting nanocomposite exhibits hierarchical stacking between the 2D nanosheets and 1D nanofibers. Specifically, the 2D nanosheets provide a thermally conductive network while the 1D nanofibers provide mechanical flexibility and robustness through entangled nanofiber–nanosheet morphologies. Experiments and density functional theory show that the nanocomposites through thickness heat transfer processes are nearly identical to that of boron nitride due to synergistic stacking of polyaramid units onto boron nitride nanosheets through van der Waals interactions. The nanocomposite sheets outperform conventional dielectric polymers in terms of mechanical properties (about 4–20‐fold increase of stiffness), light weight (density ≈1.01 g cm−3), dielectric stability over a broad range of temperature (25–200 °C) and frequencies (103–106 Hz), good dielectric breakdown strength (≈292 MV m−1), and excellent thermal management capability (about 5–24 times higher thermal conductivity) such as fast heat dissipation. [ABSTRACT FROM AUTHOR]

The low‐cost processing and uniquely structured design of conducting polymer hydrogels (CPHs), with the advantages of both conducting polymers and 3D frameworks, are the keys to their wide commercial application in next‐generation flexible solid supercapacitors. Herein, an all‐sprayable hierarchically nanostructured polyaniline–phytic acid conducting polymer hydrogel (pp‐CPHs) for upgradable art patterns and massively manufactured supercapacitor electrodes is presented. Ascribing to fully anticipating the efficient electrode–electrolyte interface of 3D porous nanostructures constructed by interconnected nanorods, the pp‐CPH‐based flexible all‐solid‐state supercapacitors exhibit an excellent areal capacitance of 91 mF cm−2 at a current density of 1 mA cm−2 and a drastically improved cycling stability with 93.5% capacitance retention after 10 000 cycles at 5 mA cm−2. In addition, the electrochemical performance of this device can be constantly maintained under various mechanical loadings such as bending and twisting. Also, this device shows a remarkable integration ability from its universal tandem and parallel connections. Unambiguously, these aforementioned merits of pp‐CPH‐based flexible all‐solid‐state supercapacitors make it an ideal maneuver for the massive fabrication of flexible power supply. [ABSTRACT FROM AUTHOR]