Flexible Polymer Research Articles

Plasticizer Design Principle of "Like Dissolves Like": Semiconductor Fluid Plasticized Stretchable Fully π-Conjugated Polymers Films for Uniform Large-Area and Flexible Deep-Blue Polymer Light-Emitting Diodes.

Physical blending of fully π-conjugated polymers (FπCPs) is an effective strategy to achieve intrinsically stretchable films for the fabrication of flexible optoelectronic devices, but easily causes phase separation, nonuniform morphology and uncontrollable photo-electronic processing. This may cause low efficiency, unstable and nonuniform emission, and poor color purity, which are undesirable for deep-blue flexible polymer light-emitting diodes (FPLEDs). Herein, a "Like Dissolves Like" design principle to prepare semiconductor fluid plasticizers (SFPs) is established and intrinsically stretchable FπCPs films via external plasticization for high-performance deep-blue FPLEDs are developed. Three fundamental requirements are proposed, "similar conjugated skeleton, similar molecular polarity, and similar electronic structures," to prepare model-matched nonpolar M1 and polar M2 plasticizers for poly(9,9-dioctylfluorene) (PFO). Large-area plasticized PFO films exhibit an efficient, narrowband, and stable ultra-deep-blue electroluminescence (FWHM < 40nm, CIE: 0.12, 0.04), uniform morphology, and excellent intrinsic stretchability (fracture strain >20% and crack-onset strain >120%). Efficient and uniform deep-blue FPLEDs based on stretchable PFO films are fabricated with a high brightness of ≈3000cd cm-2. Finally, blended PFO films exhibit outstanding stretch-deformation cycling stability of their deep-blue electroluminescent behavior, confirming the effectiveness of the "Like Dissolves Like" principle to design matched SFPs for stretchable FπCP films in flexible electronics.

Stabilizing Metal Coating on Flexible Devices by Ultrathin Protein Nanofilms.

The significant modulus difference between a metal coating and a polymer substrate leads to interface mismatches, seriously affecting the stability of flexible devices. Therefore, enhancing the adhesion stability of a metal layer on an inert polymer substrate to prevent delamination becomes a key challenge. Herein, an ultrathin protein nanofilm (UPN), synthesized by disulfide-bond-reducing protein aggregation, is proposed as a strong adhesive layer to enhance adhesion between polymer substrate and metal coating. Unlike traditional biopolymer adhesives with micrometer-scale thicknesses, the UPN layer is minimized to nanometer/single-molecular scale. Such UPN thereby effectively enhances the interfacial adhesive strength and reduces the cohesion contribution in the entire adhesion system by directly connecting two interfaces with a nearly single-molecular thickness. Using UPN as the adhesive layer, a multifunctional metal coating could be reliably adhered on flexible polymer substrates by ion sputtering, delivering unprecedented adhesion stability even under repetitive mechanical deformation. Applications of this design include reversible transparency control, tension-responsive encryption, reusable optical sensing, and wearable capacitive touch sensors. This work highlights UPN's potential to create strong bonding strength between flexible polymers and metal coatings, offering a biocompatible solution with high surface activity and low cohesion, facilitating the development of hybrid devices with stable metal nano-coating.

Dynamics of Polymer Chains in Disperse Melts: Insights from Coarse-Grained Molecular Dynamics Simulations.

Synthetic polymers have a distribution of chain lengths which can be characterized by dispersity, Đ. Their macroscopic properties are influenced by chain mobility in the melt, and controlling Đ can significantly impact these properties. In this work, we present a detailed study of the static and dynamic behavior of fully flexible polymer chains that follow the Schulz-Zimm molecular weight distribution up to Đ = 2.0 using coarse-grained molecular dynamics simulations. We analyze the behavior of test chains with molecular weights that are equal to, above, or below the molecular weight (Mw) of the melt. Static analysis shows that the conformation of these test chains remains unaffected by the heterogeneity of the surrounding chains. To study the dynamics, we computed the mean-squared displacement of test chains in melts of the same Mw and different dispersities. The mobility of test chains with N > Mw steadily increases with dispersity, due to the shorter chains contributing to early onset of disentanglement of the long chains. However, the dynamics of test chains of length N < Mw is nonmonotonic with respect to dispersity; this behavior arises from a trade-off between the increased mobility of shorter chains and the corresponding slowdown caused by the presence of longer chains. We examine the dynamic structure factor and find a weakening of tube confinement, with the effects becoming less pronounced with increasing dispersity and Mw. These findings provide insights into the rich dynamic heterogeneity of disperse polymer melts.

Hydrosilane‐Functionalized [2.2]Paracyclophane for Plasma‐Etch‐Resistant and Post‐Modifiable Poly(Para‐Xylylene)

AbstractPoly(para‐xylylene)s (PPXs), or so‐called parylenes, have become a well‐established polymer class in the conformal coating industry. Due to their transparent nature, low electrical conductivity, and high biocompatibility, they are ideal candidates for coating medical devices and other delicate electronics. However, the crosslinking of PPXs to enhance their durability is still challenging today. Expensive setups need to be used to obtain crosslinked PPXs. Furthermore, the possibility of functionalization post‐polymerization is limited. In this work, we present the synthesis of a hydrosilane functionalized [2.2]paracyclophane, which is used to obtain the corresponding hydrosilane functionalized poly(para‐xylylene) (PPX‐SiH). Through the formation of siloxane bonds during the low‐pressure chemical vapor deposition (LP‐CVD), which increases internal bonding, PPX‐SiH is obtained as a flexible and durable polymer film. The siloxane formation during the LP‐CVD is investigated through X‐ray photoelectron spectroscopy (XPS), nuclear magnetic resonance spectroscopy (NMR), and Fourier‐transform infrared spectroscopy (FTIR). Additionally, mechanistic insights into the formation of siloxane bonds are given through quantum chemical calculation. The Si‐H bonds in the polymer allow for oxidation to form bridging siloxane moieties which enhances stretchability while also increasing the resistance to organic solvents. Through the passivation of the surface during oxygen plasma treatment, PPX‐SiH becomes practically plasma‐etch‐resistant.

A single-particle energy-conserving dissipative particle dynamics approach for simulating thermophoresis of nanoparticles in polymer networks.

The transport of nanoparticles in polymer networks has critical implications in biology and medicine, especially through thermophoresis in response to temperature gradients. This study presents a single-particle energy-conserving dissipative particle dynamics (seDPD) method by integrating a single-particle model into the energy-conserving DPD model to simulate the mesoscopic thermophoretic behavior of nanoparticles in polymer matrices. We first validate the newly developed seDPD model through comparisons with analytical solutions for nanoparticle viscosity, thermal diffusivity, and hydrodynamic drag and then demonstrate the effectiveness of the seDPD model in capturing thermophoretic forces induced by temperature gradients. The results show that nanoparticles driven by the Soret forces exhibit unique transport characteristics, such as drift velocity and diffusivity, leading to a significant acceleration of nanoparticle diffusion in the polymer network, which has been known as the giant acceleration of diffusion. Quantifying how nanoparticles move in flexible polymer networks sheds light on the interaction dynamics of nanoparticles within polymer networks, providing insight into nanoparticle behavior in complex environments that could be leveraged in various applications from drug delivery to material design.

Humidity Sensing Using Polymers: A Critical Review of Current Technologies and Emerging Trends

In the post-pandemic era, human demand for a healthy lifestyle and a smart society has surged, leading to vibrant growth in the field of flexible electronic sensor technology for health monitoring. Flexible polymer humidity sensors are not only capable of the real-time monitoring of human respiration and skin moisture information but also serve as a non-contact human–machine interaction method. In addition, the development of moist-electric generation technology is expected to break free from the traditional reliance of flexible electronic devices on power equipment, which is of significant importance for the miniaturization, reliability, and environmentally friendly development of flexible devices. Currently, flexible polymer humidity sensors are playing a significant role in the field of wearable electronic devices and thus have attracted considerable attention. This review begins by introducing the structural types and working principles of various humidity sensors, including the types of capacitive, impedance/resistive, frequency-based, fiber optic, and voltage-based sensors. It mainly focuses on the latest research advancements in flexible polymer humidity sensors, particularly in the modification of humidity-sensitive materials, sensor fabrication, and hygrosensitivity mechanisms. Studies on material composites including different types of polymers, polymers combined with porous nanostructured materials, polymers combined with metal oxides, and two-dimensional materials are reviewed, along with a comparative summary of the fabrication and performance mechanisms of related devices. This paper concludes with a discussion on the current challenges and opportunities faced by flexible polymer humidity sensors, providing new research perspectives for their future development.

Combination of multivalent DR5 receptor clustering agonists and histone deacetylase inhibitors for treatment of colon cancer

Death Receptor 5 (DR5) targeted therapies offer significant promise due to their pivotal role in mediating the extrinsic pathway of apoptosis. Despite DR5 overexpression in various malignancies and the potential of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), clinical implementations of anti-DR5 monoclonal antibodies (mAbs) have been hampered by suboptimal outcomes potentially due to lack of receptor clustering.To address the limitation, we developed N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer-based conjugates integrating multiple copies of DR5-targeting peptide (cyclic WDCLDNRIGRRQCVKL; cDR5) to enhance receptor clustering and apoptosis. Three conjugates with variable number of cDR5 were prepared and denoted as PH-cDR5 (high valence), PM-cDR5 (medium valence) and PL-cDR5 (low valence). Our studies in TRAIL-sensitive and resistant cancer cell lines demonstrated that the HPMA copolymer-peptide conjugates (P-cDR5) significantly improved DR5 receptor clustering and induced apoptosis effectively. In TRAIL-sensitive colon cancer cells (COLO205, HCT-116), P-cDR5 showed efficacy comparable to anti-DR5 mAb Drozitumab (DRO), but P-cDR5 outperformed DRO in TRAIL-resistant cells (HT-29), highlighting the importance of efficient receptor clustering. In COLO205 cells PM-cDR5 exhibited an IC50 of 94 pM, while PH-cDR5 had an even lower IC50 of 15 pM (based on cDR5 equivalent concentration), indicating enhanced potency of the multivalent HPMA copolymer-based system with a flexible polymer backbone in comparison with the IC50 for TRAIL at 0.12 nM. Combining P-cDR5 with valproic acid, a histone deacetylase inhibitor, resulted in further enhancement of apoptosis inducing efficacy, along with destabilizing mitochondrial membranes and increased sensitivity of TRAIL-resistant cells. These findings suggest that attaching multiple cDR5 peptides to a flexible water-soluble polymer carrier not only overcomes the limitations of previous designs but also offers a promising avenue for treating resistant cancers, pointing toward the need for further preclinical exploration and validation of this innovative strategy.

Polymer microparticles with ultralong room-temperature phosphorescence for visual and quantitative detection of oxygen through phosphorescence image and lifetime analysis

Room-temperature phosphorescence (RTP) materials exhibiting long emission lifetimes have gained increasing attention owing to their potential applications in encryption, anti-counterfeiting, and sensing. However, most polymers exhibit a short RTP lifetime (<1 s) because of their unstable triplet excitons. Herein, a new strategy of polymer chain stabilized phosphorescence (PCSP), which yields a new kind of RTP polymers with an ultralong lifetime and a sensitive oxygen response, has been reported. The rigid polymer chains of poly(methyl mathacrylate) (PMMA) immobilize the emitter molecules through multiple interactions between them, giving rise to efficient RTP. Meanwhile, the loosely-packed amorphous polymer chains allow oxygen to diffuse inside, endowing the doped polymers with oxygen sensitivity. Flexible and transparent polymer films exhibited an impressive ultralong RTP lifetime of 2.57 s at room temperature in vacuum, which was among the best performance of PMMA. Intriguingly, their RTP was rapidly quenched in the presence of oxygen. Furthermore, RTP microparticles with a diameter of 1.63 μm were synthesized using in situ dispersion polymerization technique. Finally, oxygen sensors for quick, visual, and quantitative oxygen detection were developed based on the RTP microparticles through phosphorescence lifetime and image analysis. With distinctive advantages such as an ultralong lifetime, oxygen sensitivity, ease of fabrication, and cost-effectiveness, PCSP opens a new avenue to sensitive materials for oxygen detection.

Poly(Vinylidene Fluoride‐Hexafluoropropylene) Composites With Carbon Based Nanofillers for Electromagnetic Interference Shielding

ABSTRACTIn the current work, a series of flexible polymer matrix composites (PMCs) based on poly(vinylidene fluoride‐hexafluoropropylene) (PVDF‐HFP) as the polymer matrix and carbon nanofillers, namely single‐walled nanotubes (SWCNT) or carbon blacks (CB), were fabricated via a facile preparation method of blending and solution casting. The electrical conductivity, morphology, dielectric constant, mechanics, and electromagnetic interference (EMI) shielding properties of the composite films were adjusted by varying the carbon type (CB = Ketjenblack, Vulcan, or SWCNT = Tuball) and amount (0.1–15 wt%). The influence of the conductive nanofillers on the EMI shielding effectiveness (SE) and microwave absorbing properties in the X‐band frequency range (8–12 GHz) were investigated. By increasing the carbon content, the EMI shielding properties of the composite films were improved due to an increase in the magnitude of the electromagnetic properties. As the loading of these carbon fillers approach the percolation threshold, the dielectric constant of the composite can dramatically increase because of the construction of a microcapacitor network. However, these nanofillers/polymer composites generally have high dielectric loss near the percolation threshold due to the direct connection between carbon nanofillers. The PVDF‐HFP/Tuball composite particularly contributed low dielectric loss to the electromagnetic (EM) wave, resulting in excellent microwave absorption properties with a SE per unit thickness of 337.5 dB/mm and 2.5× less weight compared with conventional aluminum with the same SE, demonstrating the promise of using these materials as practical EMI shields.

Optimizing Contact-Less Magnetoelastic Sensor Design for Detecting Substances Accumulating in Constrained Environments

The optimization of a contact-less magnetoelastic sensing setup designed to detect substances/agents accumulating in its environment is presented. The setup is intended as a custom-built, low-cost yet effective magnetoelastic sensor for pest/bug detection in constrained places (small museums, labs, etc.). It involves a short, thin, and flexible polymer slab in a cantilever arrangement, with a short Metglas® 2826 MB magnetoelastic ribbon attached on part of its surface. A mobile phone both supports and supplies low-amplitude vibration to the slab’s free end. When vibrating, the magnetoelastic ribbon generates variable magnetic flux, thus inducing voltage in a contact-less manner into a pick-up coil suspended above the ribbon. This voltage carries specific characteristic frequencies of the slab’s vibration. If substances/agents accumulate on parts of the (suitably coated) slab surface, its mass distribution and, hence, characteristic frequencies change. Then, simply monitoring shifts of such frequencies in the recorded voltage enables the detection of accumulating substances/agents. The current work uses extensive testing via various vibration profiles and load positions on the slab, for statistically evaluating the sensitivity of the mass detection of the setup. It is shown that, although this custom-built substance/agent detector involves limited (low-cost) hardware and a simplified design, it achieves promising results with respect to its cost.

Chemical-Physical Synergistic Assembly of MXene/CNT Nanocoatings in Silicone Foams for Reliable Piezoresistive Sensing in Harsh Environments.

Owing to their high sensitivity across a wide stress range, mechanical reliability, and rapid response time, flexible polymer foam piezoresistive sensors have been extensively used in various fields. The reliable application of these sensors under harsh environments, however,is severely limited by structural devastation and poor interfacial bonding between polymers and conductive nanoparticles. To address the above issues, robust MXene/CNT nanocoatings on the foam surface, where the chemical assembly of MXene nanosheets and the physical anchoring of CNTs lead to strong interfacial bonding, are designed and described, which endows foams with structural reliability and unexpected multi-functionalities without compromising their instinct properties. The optimized foam nanocomposites thus maintain outstanding wide-temperature flexibility (-60-210 °C) and elasticity (≈3% residual strain after 1000 cycles). Moreover, the nanocomposites display good sensitivity at a relatively wide stress range of 0-70% and remarkable stability under acidic and alkaline settings. Furthermore, the foams with exceptional fire resistance (UL-94 V-0 rating) can provide stable sensing behavior (over 300 cycles) even after being exposed to flames for 5 s, making them one of the most reliable sensing materials so far. Clearly, this work widens applications of flexible piezoresistive sensors based on silicone foam nanocomposites for various harsh environments.

A photocurable ultra-tough eutectic gel with coordination crosslinking used for wearable sensors and TENG flexible electrodes

Flexible polymer molecular chains are of great interest to researchers in the field of flexible wearable electronics due to their unrivaled flexibility and ductility. However, achieving high toughness, high elasticity, environmental stability and easy machining of flexible electronic materials remains a challenge. In this study, we present a photocurable eutectic gel mainly composed of DMAPS, AAc, Zr4+ and deep eutectic solvents (DES). Due to the strong coordination between zirconium ions and polymer networks, the gel can be endowed with excellent properties, such as excellent tensile strength (1.14 MPa), low hysteresis (5 kJ·m−3) and good adhesion (above 40 kPa). DES can not only give the gel good electrical conductivity, but also maintain the stability of the gel to ensure that the leakage or volatilization of the solvent will not occur in use. The properties mentioned above allow the gel to achieve a sensitivity factor of up to 1.7 over a small strain range, demonstrating its potential applications in the field of flexible strain sensors and triboelectric flexible electrode materials. What’s more, the gel can be used to prepare complex geometric shapes with high precision through digital light processing (DLP) based 3D printing technology. Therefore, this work introduces a novel approach for the development of highly stable flexible wearable devices, which has the potential to expand the applications of eutectic gels.

Flexible Asymmetrically Transparent Conductive Metamaterial Electrode Based on Photonic Nanojet Arrays

AbstractFlexible transparent electrodes, encompassing the combination of optical transparency and electrical conductivity, empower numerous optoelectronic applications. While the main efforts nowadays concentrate on developing wire meshes and conductive oxides, those technologies are still in a quest to find a balance between price, performance, and versatility. Here we propose a new platform, encompassing the advantages of nanophotonic design and roll‐to‐roll large‐scale lithography fabrication tools, granting an ultimate balance between optical, electrical, and mechanical properties. The design is based on an array of silica microspheres deposited on a patterned thin aluminum film attached to a flexible polymer matrix. Microspheres are designed to squeeze 80% light through nanoscale apertures with the aid of the photonic nanojet effect given the light impinges the structure from the top. The photonic structure blocks the transmission for the backpropagation direction thus granting the device with the high 5‐fold level of asymmetry. The patterned layer demonstrates a remarkable 2.8 Ω sq−1 sheet resistance comparable to that of a continuous metal layer. The high conductivity is shown to be maintained after a repeatable application of strain on the flexible electrode. Such remarkable optical, mechanical and electrical properties, makes the demonstrated device an essential component for applications, where such attributes are critically required.

Folding behaviors of two-dimensional flexible polymers.

Unlike one-dimensional polymers, the theoretical framework on the behaviors of two-dimensional (2D) polymers is far from completeness. In this study, we model single-layer flexible 2D polymers of different sizes and examine their scaling behaviors in solution, represented by Rg ∼ Lν, where Rg is the radius of gyration and L is the side length of a 2D polymer. We find that the scaling exponent ν is 0.96 for a good solvent and 0.64 for under poor solvent condition. Interestingly, we observe a previously unnoticed phenomenon: under intermediate solvent conditions, the 2D polymer folds to maintain a flat structure, and as L becomes larger, multiple folded structures emerge. We introduce a shape parameter Q to diagram the relationship of folded structures with the polymer size and solvent condition. Theoretically, we explain the folding transitions by the competition between bending and solvophobic free energies.

Positional Isomerism Toward Tunable Organic Afterglow and Reversible Photoactivation Behavior for Anti‐Counterfeiting and Encryption

AbstractAchieving amorphous polymers with ultralong room‐temperature phosphorescence (RTP), tunable organic afterglow, and reversible photoactivation behavior is highly desirable for practical applications but challenging. Herein, simple positional isomers with three carboxyl groups located in the ortho, meta, and para positions of the triphenylamine skeleton are designed and synthesized. By physically blending with the poly(vinyl alcohol) matrix, these isomers show ultralong RTP properties, among which the meta‐isomer has the longest RTP lifetime (620.1 ms). Theoretical calculations reveal that the more efficient intersystem crossing, the slower radiative decay rate of the lowest triplet excitons, and stronger intermolecular hydrogen‐bonding interactions should be responsible for the superior RTP property of meta‐isomer. Furthermore, the tunable organic afterglow is readily realized via a triplet‐to‐singlet energy transfer process. More impressively, the meta and para isomers exhibit reversible photoactivated ultralong RTP properties after embedding into the rigid poly(methyl methacrylate) matrix. Finally, amorphous and flexible polymer films prepared from these positional isomers show potential applications in advanced anti‐counterfeiting and multilevel encryption through subtly combining ultralong RTP lifetime, tunable organic afterglow, and reversible photoactivation behavior.

Silage harvesting for small farms by using vacuum sealing in flexible polymer containers on a converted trailer

The article presents an analysis of milk production in Kazakhstan and identifies the reason for its low level, which is due to deficient feed, especially in small farms and in the private sector. The difficulty of saving the limited silage volume is due to the lack of preparation technology for preventing spoilage. The objective of this work is to complete the necessary equipment of a mobile tractor-trailer to reduce the specific energy consumption when preparing silage in flexible containers using a vacuum seal to increase the productivity of dairy cattle farming in smallholder and the private sector of the Republic. The basic rational parameters for sealing the silage by vacuum in the field on a mobile tractor-trailer for ease of transport and storage are obtained: silage weight in a flexible container – 769.6 kg, geometric dimensions of the sealed container by height (0.90 m), width (0.85 m) and length (0.85 m). The efficiency of the specific energy consumption of the proposed method for silage preparation is established at 35% compared with the traditional method. The recommended technology of silage preparation in flexible containers will be possible when conventional tractor-trailers are retrofitted with standard portable equipment (internal combustion engine-based (ICE) electric generator, vacuum pump, film welder).

An acoustic nanogenerator based on porous PDMS/ZnO/PVDF-TrFE structure for self-powered intermediated-frequency sound monitoring

Abstract Sound energy is widely present in natural environment, nowadays predominantly collected using voluminous and heavy rigid devices, limiting their portability. Till now, there are few reports about using flexible materials to collect sound energy, and it is usually susceptible to environmental humidity. This study combines flexible polymer polydimethylsiloxane (PDMS), piezoelectric material polyvinylidene difluoride trifluoroethylene (PVDF-TrFE), nano zinc oxide (ZnO), and conductive carbon nanotubes (CNTs) to fabricate a porous nano ZnO/PVDF-TrFE/CNTs PDMS sound-driven nanogenerator (PZPCP SNG). It amalgamates frictional and piezoelectric effects: its porous structure enables efficient collection of vibration and frictional energy generated by sound waves; the piezoelectric effect of PVDF-TrFE and nano ZnO facilitates the conversion of acoustic mechanical energy, collectively enhancing the generator's output. Experimental optimization yields the best production conditions, achieving optimal outputs of 481.1 mV (open-circuit voltage), 209.13 nA (short-circuit current) under 400 Hz/125 dB sound stimuli, with a surface power density of 9.1 µW/m² (volumetric power density of 2.28 mW/m³). And it can convert sound ranging from 63-3000 Hz. With hardware circuitry, up to 5 series-connected light-emitting diodes (LEDs) can be illuminated within the circuit, demonstrating a certain degree of sound recognition capability. The proposed PZPCP SNG design is simple, effective, and lightweight, enabling flexible and stable intermediated-frequency acoustic energy harvesting. Its hydrophobic structural characteristics render it adaptable to various humidity, presenting a new approach toward widespread low-power sound detection and self-powering applications.

Chain rigidity controlled aggregation ability and solid-state microstructures for efficient stretchable conjugated polymer films

Stretchable conjugated polymer films with good electrical performance under mechanical deformation are highly desirable for soft electronics. However, the mechanical and electrical properties of these films, particularly in conjugated polymer:elastomer blends, are not fully understood at molecular level. This study explores the relationships among molecular structure, aggregation ability, film microstructure, and the electrical/mechanical properties of three diketopyrrolopyrrole -based conjugated polymers (P1, P2, P3) with decreasing backbone rigidity and their corresponding polymer:elastomer blends. The most flexible polymer P3 shows strong aggregation, which forms highly crystalline fibers to produce fragile neat film and produces large isolated crystallites restricting charge transport in blend film. As chain rigidity increases, the P1 and P2 polymers show weaker aggregation, and produce smaller crystallites in neat films with enhanced ductility. P1 and P2 based blend films display nanocrystallites polymer networks with dispersed elastomer domains. As a result, we achieved near-constant charge mobility before and after stretching under 50 % strain for P2-based blend films with well-controlled pathways for both charge transport and energy dissipation. This study demonstrates the critical role of backbone rigidity in regulating the properties of stretchable conjugated polymer films, paving the way for more reliable and deformable materials in soft electronics.

Synergistic Reduction and Oxidation Resistant Interface Modifier for High‐Voltage and High‐Loading Solid‐State Lithium Batteries

AbstractSolid‐state batteries (SSBs) with high‐voltage cathodes and Li‐anodes offer promising energy density and safety for next‐generation batteries. However, poor contact and electrochemical instability of solid electrolyte interfaces hinder their long‐term performance. Traditional rigid solidification interlayers possess restricted capability to address these issues. Herein, a composite buffer interlayer (CBI) with localized high‐concentration electrolytes (LHCEs) in a flexible polymer scaffold, tackling contact and stability problems and ensuring a perfect interface is developed. The extended electrochemical window provides it with synergistic antioxidation and antireduction capabilities, making it compatible with high‐voltage cathodes and Li anodes, while an in situ formed LiF‐Li3N rich inorganic interface ensures uniform lithium deposition and prevents dendrite formation. This CBI enables lithium symmetric cells to achieve a super high critical current density of 7.2 mA cm−2. Most impressively, coupled with a high‐voltage LiNi0.83Co0.12Mn0.05O2 cathode (NCM83), the full cell achieves 94.1% capacity retention after 125 cycles (coulombic efficiency &gt;99.8%) at a mass loading of 14.6 mg cm−2 and a high voltage of 4.45 V. Additionally, a pouch cell with 17.2 mg cm−2 NCM83 achieves an initial discharge capacity of 3.82 mAh cm−2 an superior cycling stability (75 cycles, 89% capacity retention), showcasing the practical potential of LHCE‐CBI enabled SSBs.

CoFe2O4-BaTiO3 core-shell-embedded flexible polymer composite as an efficient magnetoelectric energy harvester

Flexible magnetoelectric (ME) generators gained immense interest due to the broad applications in wearable and Internet of Things (IoT)-based devices. The key to achieving high energy conversion performance of 0–3 type ME composite films is the prevention of filler aggregation in the polymer matrix and accessing the full potential of intrinsic properties of filler. To achieve high performance, a flexible ME composite film was fabricated by homogeneous distribution of magnetostrictive CoFe2O4-BaTiO3 core-shell (CBCS) fillers into piezoelectric polyvinylidene fluoride (PVDF) polymer. The ME composite film generates an enhanced energy conversion efficiency by optimizing the shell thickness of CBCS and maximizing the electroactive β-phase at the BaTiO3 shell-PVDF interfacial region. The observed ME coefficient of the film reached up to 710 mV/cm∙Oe. Multiphysics simulations based on the finite element analysis were adopted to investigate the role of BaTiO3 shell thickness on the performance of ME film. This study paves the way to achieve higher filler loading content in the ME composite films to develop an efficient, flexible ME generator for eco-friendly permanent power sources.