Dynamic Polymers for Transient Electronics.

The emergent transient electronics that can be destroyed or degraded harmlessly under an environmental stimulus are attracting extensive attentions toward eco‐friendly electronic devices and confidential communication applications. However, currently available transient electronics are limited by the poor recyclability of components, which fails to meet the ever‐increasing demands of advanced electronic devices. Here, this work reports a fully recyclable transient electronic device based on a multi‐layered architecture, comprising a liquid metal (LM) as the conductor and a NaOH solution‐embedded paraffin composite (NPC) as the degradation agent. Upon thermally triggered by the bottom heater, the middle‐layer LM circuit and the top NPC layer melt, releasing the aqueous alkali to destroy the circuit at a quick transient rate (46 ± 4 s). Afterward, both the free LM and paraffin are recycled at extremely high efficiencies, that is, 98% for LM owing to the self‐aggregation and fluidic nature, 95% for paraffin arising from the low melting point and good recoverability. The successful integration of transience and recycling abilities dramatically improves the feasibility of transient electronics in real applications, as further demonstrated in a radio‐frequency transmission device and a remote destructible memristor, which hold great promises for confidential data storage devices and next‐generation electronics.

Rapid development of electronic technology shortens the development time for new products and accelerates the obsolescence of consumer electronics, resulting in the explosive growth of electronic waste that is difficult to recycle and hazardous to the environment and human health. Transient electronics that can dissolve in water may potentially be adopted to tackle the issues of electronic waste; however, promising approaches to yield large-scale and high-performance transient consumer electronics have not yet been developed. Here, the joint effect of galvanic corrosion and redeposition has been utilized to develop bimetallic transient nanocomposites, which can be printed and water-sintered to yield high-performance transient PCB circuits with excellent electrical conductivity and mechanical robustness. The entire sintering process requires no external energy and strict environmental conditions. The achieved PCB circuits offer a conductivity of 307,664.4 S/m that is among the highest in comparison with other printed transient circuits. The supreme performance of the transient circuits eventually leads to the first dissolvable smartwatch that offers the same functions and similar performance as conventional smartwatches and dissolves in water within 40 h. The joint effect of galvanic corrosion and redeposition between two metals with distinct activities leads to novel nanocomposites and processing techniques of transient electronics. The resulting high-performance transient devices may reshape the appearance of consumer electronics and reform the electronics recycling industry by reducing recycling costs and minimizing environmental pollution and health hazard.

Transient electronics with degradability or dissolvability on demand possess remarkable characteristics for wearable, bioelectronic, and implanted electronic devices. While synthetic materials have made significant progress in degradability and stretchability, they suffer from intrinsic limitations, including low degradation rates, poor mechanical compliance, and high production cost, which restrict the growth of transient electronic devices. Herein, a versatile fabrication strategy is presented for transient electronics that combine a resilient biopolymer substrate (gelatin biogels) with liquid metal (Galinstan). The circuits made from gelatin biogel‐based and liquid metal are mechanically resilient and durable, exhibiting good compliance with irregular and deformable surfaces, and thus can withstand long‐term exposure to dynamic deformation (about 60 000 cycles at a strain of 50%). More importantly, gelatin biogels are naturally derived and endowed with thermally reversible gelling, which enables on‐demand rapid dissolution and recycling of the materials. As a proof‐of‐concept, transient circuit‐based capacitive sensors, which can be degraded within 20 s, are fabricated for monitoring finger touching, morse code generation, and electrical touchpad. Such a strategy provides a guideline for designing transient electronics with a combination of biopolymer gels and liquid metal, and this approach is anticipated to find applications in human–machine interfaces and wearable devices.

Foundry-based routes to transient silicon electronic devices have the potential to serve as the manufacturing basis for "green" electronic devices, biodegradable implants, hardware secure data storage systems, and unrecoverable remote devices. This article introduces materials and processing approaches that enable state-of-the-art silicon complementary metal-oxide-semiconductor (CMOS) foundries to be leveraged for high-performance, water-soluble forms of electronics. The key elements are (i) collections of biodegradable electronic materials (e.g., silicon, tungsten, silicon nitride, silicon dioxide) and device architectures that are compatible with manufacturing procedures currently used in the integrated circuit industry, (ii) release schemes and transfer printing methods for integration of multiple ultrathin components formed in this way onto biodegradable polymer substrates, and (iii) planarization and metallization techniques to yield interconnected and fully functional systems. Various CMOS devices and circuit elements created in this fashion and detailed measurements of their electrical characteristics highlight the capabilities. Accelerated dissolution studies in aqueous environments reveal the chemical kinetics associated with the underlying transient behaviors. The results demonstrate the technical feasibility for using foundry-based routes to sophisticated forms of transient electronic devices, with functional capabilities and cost structures that could support diverse applications in the biomedical, military, industrial, and consumer industries.

In this study, a flexible strain sensor is devised using corrugated bilayer thin films consisting of poly(3-hexylthiophene) (P3HT) and poly(3,4-ethylenedioxythiophene)-polystyrene(sulfonate) (PEDOT:PSS). In previous studies, the P3HT-based photoactive non-corrugated thin film was shown to generate direct current (DC) under broadband light, and the generated DC voltage varied with applied tensile strain. Yet, the mechanical resiliency and strain sensing range of the P3HT-based thin film strain sensor were limited due to brittle non-corrugated thin film constituents. To address this issue, it is aimed to design a mechanically resilient strain sensor using corrugated thin film constituents. Buckling is induced to form corrugation in the thin films by applying pre-strain to the substrate, where the thin films are deposited, and releasing the pre-strain afterwards. It is known that corrugated thin film constituents exhibit different optical and electronic properties from non-corrugated ones. Therefore, to design the flexible strain sensor, it was studied to understand how the applied pre-strain and thickness of the PEDOT:PSS conductive thin film affects the optical and electrical properties. In addition, strain effect was investigated on the optical and electrical properties of the corrugated thin film constituents. Finally, flexible strain sensors are fabricated by following the design guideline, which is suggested from the studies on the corrugated thin film constituents, and the DC voltage strain sensing capability of the flexible strain sensors was validated. As a result, the flexible strain sensor exhibited a tensile strain sensing range up to 5% at a frequency up to 15 Hz with a maximum gauge factor ~7.

Degradable features are highly desirable to advance next-generation organic mixed ionic-electronic conductors (OMIECs) for transient bioinspired artificial intelligence devices. It is highly challenging that OMIECs exhibit excellent mixed ionic-electronic behavior and show degradability simultaneously. Specially, in OMIECs, doping is often a tradeoff between structural disorder and charge carrier mobilities. Here, we describe a regiochemistry-driven backbone curvature approach to prepare OMIECs, enabling doped state ordered within efficient ionic-electronic conduction in organic electrochemical transistors (OECTs) and presenting degradable characteristics. Significantly, i-3gTIT shows an outstanding mobility (1.99 cm2 V-1 s-1) and μC* (302 F V-1 cm-1 s-1), and presents higher disorder-tolerance upon doping and faster degradation behavior than its regioisomer, o-3gTIT. Especially, the resulting OECT-based inverter shows a high voltage gain of 31.6 V V-1 at a low driving voltage of 0.6 V. Moreover, we demonstrate an application of transient OECT, i. e., biodegradable solid-state electrolyte of OECT-based artificial synapses. Remarkably, the regiochemistry-driven film crystallinity modulation enables the conversion from volatile to non-volatile operation in such synapses. The transient synapse based on i-3gTIT achieves over 90 % recognition accuracy for small digit handwritten images, showing potential in security neuromorphic computing. Our work is the first presentation enabling excellent mixed conduction of OMIECs with degradable features for transient bioinspired electronics.

A sustainable and efficient multicatalytic chemical transformation approach is devised for the development of all-biobased environmentally adaptable polymers and gels with multifunctional properties. The catalytic system, utilizing Lignin aluminum nanoparticles (AlNPs)-aluminum ions (Al3+ ), synergistically combines multiple catalytic cycles to create robust, mechanically stable, and versatile organohydrogels. Single catalytic cycles alone fail to achieve desired results, highlighting the importance of cooperatively combining different cycles for successful outcomes. The transformation involves free radical crosslinking, reversible quinone-catechol reactions, and an autocatalytic mechanism, resulting in a dual crosslinking strategy that incorporates both covalent and ionic crosslinking. This approach creates a dynamic gel system with combined energy dissipation and storage mechanisms. The engineered organohydrogels demonstrate vital multifunctionalities such as good thermal stability, self-healing, and adhesive properties, flame-retardancy, mechanical resilience and durability, conductivity, viscoelastic properties, environmental adaptability, and resistance to extreme conditions such as freezing and drying. The developed catalytic technology and resulting gels hold significant potential for applications in flexible electronics, energy storage, actuators, and sensors.

We report a flexible hydrogen sensor, composed of WS2 nanosheet–Pd nanoparticle composite film, fabricated on a flexible polyimide substrate. The sensor offers the advantages of light-weight, mechanical durability, room temperature operation, and high sensitivity. The WS2–Pd composite film exhibits sensitivity (R1/R2, the ratio of the initial resistance to final resistance of the sensor) of 7.8 to 50 000 ppm hydrogen. Moreover, the WS2–Pd composite film distinctly outperforms the graphene–Pd composite, whose sensitivity is only 1.14. Furthermore, the ease of fabrication holds great potential for scalable and low-cost manufacturing of hydrogen sensors.

Gels that are freeze-resistant and heat-resistant and have high ultimate tensile strength are desirable in practical applications owing to their potential in designing flexible energy storage devices, actuators, and sensors. Here, a simple method for fabricating ionic liquid (IL)-based click-ionogels using thiol-ene click chemistry under mild condition is reported. These click-ionogels continue to exhibit excellent mechanical properties and resilience after 10,000 fatigue cycles. Moreover, due to several unique properties of ILs, these click-ionogels exhibit high ionic conductivity, transparency, and nonflammability performance over a wide temperature range (-75° to 340°C). Click-ionogel-based triboelectric nanogenerators exhibit excellent mechanical, freeze-thaw, and heat stability. These promising features of click-ionogels will promote innovative applications in flexible and safe device design.

Biological systems inspire the design of high-performance biomimetic materials, yet replicating their synergistic interactions and hierarchical structures remains challenging. Here, we present an orthogonal photochemistry-mediated strategy for one-step fabrication of muscle-inspired protein materials. This approach integrates covalent, electrostatic, and hydrogen-bonding interactions to form robust multinetwork architectures within hierarchically organized protein matrices. Prestretching enhances molecular alignment, yielding anisotropic materials with a factor of 3.0, tensile strengths up to 300 MPa, toughness over 22 MJ m-3, and a fatigue threshold of 760 J m-2─surpassing natural proteins such as wool, cotton, and silk. The rapid (∼20 s), precisely controllable process supports scalable 3D manufacturing of continuous fibers exceeding 10 m. Beyond mechanical robustness, the materials dynamically respond to force, humidity, and pH, mimicking biological tissues. As a proof of concept, the fibers function as artificial muscles and flexible capacitive sensors, highlighting their potential for advanced applications in biomaterials, bioengineering, and soft electronics.

The performance of flexible and stretchable sensors relies on the optimization of both the flexible substrate and the sensing element, and their synergistic interactions. Herein, a novel strategy is reported for cost‐effective and scalable manufacturing of a new class of porous materials as 3D flexible and stretchable piezoresistive sensors, by assembling carbon nanotubes onto porous substrates of tunable Poisson ratios. It is shown that the piezoresistive sensitivity of the sensors increases as the substrate's Poisson's ratio decreases. Substrates with negative Poisson ratios (auxetic foams) exhibit significantly higher piezoresistive sensitivity, resulting from the coherent mode of deformation of the auxetic foam and enhanced changes of tunneling resistance of the carbon nanotube networks. Compared with conventional foam sensors, the auxetic foam sensor (AFS) with a Poisson's ratio of –0.5 demonstrates a 300% improvement in piezoresistive sensitivity and the gauge factor increases as much as 500%. The AFS has high sensing capability, is extremely robust, and capable of multimodal sensing, such as large deformation sensing, pressure sensing, shear/torsion sensing, and underwater sensing. AFS shows great potential for a broad range of wearable and portable devices applications, which are described by reporting on a series of demonstrations.

Enhanced performance of fiber-based perovskite solar cell achieved by multi-functional high polymer doping strategy

Flexible sensors based on the highly elastic Polyurethane (PU)-containing textile substrates have been frequently incorporated in enormous wearable applications. However, the desirable sensing properties such as stable sensitivity, small hysteresis and good repeatability depend on the mechanical resilience of the textile substrates. This paper conducts a systematic investigation into the mechanical hysteresis of the PU-containing textile substrates, from fibers to yarns and then fabrics. The impact of fiber materials, yarn structures, and fabric constructions on the overall tensile properties of the PU-containing substrates were examined. It was found that fibers of high elasticity, stable yarn structure with excellent recovery, as well as appropriate fabric construction are effective to reduce the mechanical hysteresis of the textile substrates. Coated strain sensors based on different substrates were then fabricated. Results show that smaller mechanical hysteresis of the PU-containing substrates generally led to lower electromechanical hysteresis and better repeatability of sensors. This paper gives all-round consideration of the fibers and structure features of substrates to provide recommendation for reducing mechanical and electromechanical hysteresis of sensors based on PU-containing textiles and benefiting the design and optimization of other flexible sensors.

Scalable manufacturing of real-time self-healing strain sensors based on brominated natural rubber

Flexible electronics have received considerable attention in academies and industries for their promising applications in enormous fields, such as flexible displays, wearable sensors, artificial skins, and flexible energy devices. Challenges remain in developing a flexible and scalable manufacturing method to facilitate the fabrication of multi-functional structures in a flexible electronic system. Nanoimprint lithography is a high resolution and low-cost approach to fabricate nanostructures over a large area. This paper reviews recent progress of nanoimprint lithography and its applications in flexible electronics. The basic principles, classification, research focus, and critical issues of nanoimprint lithography are elaborated. Then, the advantages of nanoimprint lithography are demonstrated in several typical applications related to flexible electronics, including conductive films, optoelectronic devices, flexible sensors, energy harvesting and storage devices, and bioinspired electronic devices. Finally, the challenges and perspectives of nanoimprint lithography in flexible electronic systems are discussed.