A review on emerging biodegradable polymers for environmentally benign transient electronic skins

Journal of Materials Science - Biodegradable or transient electronics is an emerging technology whose key characteristic is an ability to dissolve, resorb, physically disappear or disintegrate in...     

A Fully Biodegradable Battery for Self‐Powered Transient Implants

Biodegradable transient devices represent an emerging type of electronics that could play an essential role in medical therapeutic/diagnostic processes, such as wound healing and tissue regeneration. The associated biodegradable power sources, however, remain as a major challenge toward future clinical applications, as the demonstrated electrical stimulation and sensing functions are limited by wired external power or wireless energy harvesters via near‐field coupling. Here, materials' strategies and fabrication schemes that enable a high‐performance fully biodegradable magnesium–molybdenum trioxide battery as an alternative approach for an in vivo on‐board power supply are reported. The battery can deliver a stable high output voltage as well as prolonged lifetime that could satisfy requirements of representative implantable electronics. The battery is fully biodegradable and demonstrates desirable biocompatibility. The battery system provides a promising solution to advanced energy harvesters for self‐powered transient bioresorbable implants as well as eco‐friendly electronics.     

25th Anniversary Article: Materials for High‐Performance Biodegradable Semiconductor Devices

We review recent progress in a class of silicon‐based electronics that is capable of complete, controlled dissolution when immersed in water or bio‐fluids. This type of technology, referred to in a broader sense as transient electronics, has potential applications in resorbable biomedical devices, eco‐friendly electronics, environmental sensors, secure hardware systems and others. New results reported here include studies of the kinetics of hydrolysis of nanomembranes of single crystalline silicon in bio‐fluids and aqueous solutions at various pH levels and temperatures. Evaluations of toxicity using live animal models and test coupons of transient electronic materials provide some evidence of their biocompatibility, thereby suggesting potential for use in bioresorbable electronic implants.     

Laser-Triggered Degradation of Silicon Circuits by Lithiation and Moisture Uptake for On-Demand Transient Electronics

Data security risks of unauthorized access of confidential information have attracted considerable attention. Transient electronics capable of physical disappearance or disintegration upon external stimuli could potentially offer an alternative solution at the device level. Despite great advances, smart, efficient, wireless, and nonrecoverable degradation of foundry-compatible silicon (Si)-integrated circuit (IC) chips remains a challenge. Herein, a laser-triggered degradation of Si circuits by lithiation and moisture uptake is proposed. By integrating IC chips with a small amount of lithium sources and a fluidic reservoir consisting of hygroscopic materials, on-demand, wireless, rapid, and complete degradation of Si IC chips built at 600 nm node is achieved upon activation by laser irradiation. This work paves a new route to accomplish smart, tether-free, and thorough degradation of devices compatible with existing foundry processes, offering an essential baseline for the development of intelligent transient electronics for secured hardware.     

Flammable carbon nanotube transistors on a nitrocellulose paper substrate for transient electronics

Transient electronics represent an emerging class of technology comprising materials that can vanish in a controlled manner in response to stimuli. In contrast to conventional electronic devices that are designed to operate over the longest possible period, transient electronics are defined by operation typically over a short and well-defined period; when no longer needed, transient electronics undergo self-deconstruction and disappear completely. In this work, we demonstrate the fabrication of thermally triggered transient electronic devices based on a paper substrate, specifically, a nitrocellulose paper. Nitrocellulose paper is frequently used in acts of magic because it consists of highly flammable components that are formed by nitrating cellulose by exposure to nitric acid. Therefore, a complete and rapid destruction of electronic devices fabricated on nitrocellulose paper is possible without producing any residue (i.e., ash). The transience rates can be modified by controlling radio frequency signal-induced voltages that are applied to a silver (Ag) resistive heater, which is stamped on the backside of the nitrocellulose paper. The Ag resistive heater was prepared by a simple, low-cost stamping fabrication, which requires no harsh chemicals or complex thermal treatments. For the electronics on the nitrocellulose paper substrate, we employed semiconducting carbon nanotube (CNT) network channels in the transistor for superior electrical and mechanical properties.

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Biodegradable Electronic Systems in 3D,Heterogeneously Integrated Formats

Biodegradable electronic systems represent an emerging class of technology with unique application possibilities, from temporary biomedical implants to “green” consumer gadgets. This paper introduces materials and processing methods for 3D, heterogeneously integrated devices of this type, with various functional examples in sophisticated forms of silicon‐based electronics. Specifically, techniques for performing multilayer assembly by transfer printing and for fabricating layer‐to‐layer vias and interconnects by lithographic procedures serve as routes to biodegradable, 3D integrated circuits composed of functional building blocks formed using specialized approaches or sourced from commercial semiconductor foundries. Demonstration examples range from logic gates and analog circuits that undergo functional transformation by transience to systems that integrate multilayer resistive sensors for in situ, continuous electrical monitoring of the processes of transience. The results significantly expand the scope of engineering options for biodegradable electronics and other types of transient microsystem technologies.     

Fabricating functional circuits on 3D freeform surfaces via intense pulsed light-induced zinc mass transfer

Deployment of functional circuits on a 3D freeform surface is of significant interest to wearable devices on curvilinear skin/tissue surfaces or smart Internet-of-Things with sensors on 3D objects. Here we present a new fabrication strategy that can directly print functional circuits either transient or long-lasting onto freeform surfaces by intense pulsed light-induced mass transfer of zinc nanoparticles (Zn NPs). The intense pulsed light can locally raise the temperature of Zn NPs to cause evaporation. Lamination of a kirigami-patterned soft semi-transparent polymer film with Zn NPs conforming to a 3D surface results in condensation of Zn NPs to form conductive yet degradable Zn patterns onto a 3D freeform surface for constructing transient electronics. Immersing the Zn patterns into a copper sulfate or silver nitrate solution can further convert the transient device to a long-lasting device with copper or silver. Functional circuits with integrated sensors and a wireless communication component on 3D glass beakers and seashells with complex surface geometries demonstrate the viability of this manufacturing strategy.     

Flashlight-material interaction for wearable and flexible electronics

Light-material interaction has received significant attention for wearable electronics because of its exceptional ability to excite multi-physical, transient, and non-equilibrium photon interactions in a spatiotemporally controlled manner. It has realized unique photothermal and photochemical reactions with various types of materials, including metal nanomaterials, ceramics, graphene, polymers, and perovskites, enabling the substantial performance improvement of soft electronics without damaging a temperature-sensitive substrates. Among the numerous optical sources, flash lamps have been considered to be a suitable platform for commercial applications owing to their excellent light-output efficiency, rapid processing capability, and outstanding compatibility with large-scale roll-to-roll manufacturing. These exclusive features offer considerable advantages in a broad range of wearable and flexible electronics such as solar cells, thin-film-transistors, optoelectronics, and sensors on polymer substrates compared to the conventional high-temperature microfabrication processes. The flash lamp technology has consistently advanced to provide novel concepts of nanomaterials/devices with unlimited form factors and strategies for future wearable electronics. Here, the recent progress in the field of flashlight-material interaction for soft electronics is summarized with regard to the process parameters, materials, and devices, together with the latest updates on the flash lamp technology.     

Liquid Metal–Based Soft Microfluidics

Motivated by the increasing demand of wearable and soft electronics, liquid metal (LM)‐based microfluidics has been subjected to tremendous development in the past decade, especially in electronics, robotics, and related fields, due to the unique advantages of LMs that combines the conductivity and deformability all‐in‐one. LMs can be integrated as the core component into microfluidic systems in the form of either droplets/marbles or composites embedded by polymer materials with isotropic and anisotropic distribution. The LM microfluidic systems are found to have broad applications in deformable antennas, soft diodes, biomedical sensing chips, transient circuits, mechanically adaptive materials, etc. Herein, the recent progress in the development of LM‐based microfluidics and their potential applications are summarized. The current challenges toward industrial applications and future research orientation of this field are also summarized and discussed.     

Transient Light‐Emitting Diodes Constructed from Semiconductors and Transparent Conductors that Biodegrade Under Physiological Conditions

Transient forms of electronics, systems that disintegrate, dissolve, resorb, or sublime in a controlled manner after a well‐defined operating lifetime, are of interest for applications in hardware secure technologies, temporary biomedical implants, “green” consumer devices and other areas that cannot be addressed with conventional approaches. Broad sets of materials now exist for a range of transient electronic components, including transistors, diodes, antennas, sensors, and even batteries. This work reports the first examples of transient light‐emitting diodes (LEDs) that can completely dissolve in aqueous solutions to biologically and environmentally benign end products. Thin films of highly textured ZnO and polycrystalline Mo serve as semiconductors for light generation and conductors for transparent electrodes, respectively. The emitted light spans a range of visible wavelengths, where nanomembranes of monocrystalline silicon can serve as transient filters to yield red, green, and blue LEDs. Detailed characterization of the material chemistries and morphologies of the constituent layers, assessments of their performance properties, and studies of their dissolution processes define the underlying aspects. These results establish an electroluminescent light source technology for unique classes of optoelectronic systems that vanish into benign forms when exposed to aqueous conditions in the environment or in living organisms.     

A Solid-State Synchronous Switch for Use in Transient and Modeling Stuies

This paper describes a new synchronous switch employing solid-state electronics, that extends the usefulness of the CRO in viewing transient phenomena in electrical circuits by means of a repetitive trace on the CRO. This device is particularly useful in normal research projects and has a unique place in repetitive and "one-time" switching in power system models such as the conventional transient analyzer and the newer EHV simulators.     

Optical nutation in GaAs/GaxA11−xAs quantum well structures

Abstract

The possibility of occurrence of the coherent optical transient effect known as optical nutation has been analytically established in the semiconductor quantum well (QW) structure, namely GaAs/Ga_xA1_1?xAs most extensively used in optical electronics. Ultra-short-pulse low-intensity band-to-band excitation of electrons to the 1s Wannier-Mott exciton state of the crystal has been considered to play an important role in the coherent radiation—QW interaction. Numerical estimations of the complex optical susceptibility and the transmitted intensity under the transient regime reveal ringing behaviour confirming the occurrence of optical nutation in III-V semiconducting QW structures.     

Biosafe,Eco‐Friendly Levan Polysaccharide toward Transient Electronics

New options in the material context of transient electronics are essential to create or expand potential applications and to progress in the face of technological challenges. A soft, transparent, and cost‐effective polymer of levan polysaccharide that is capable of complete, programmable dissolution is described when immersed in water and implanted in an animal model. The results include chemical analysis, the kinetics of hydrolysis, and adjustable dissolution rates of levan, and a simple theoretical model of reactive diffusion governed by temperature. In vivo experiments of the levan represent nontoxicity and biocompatibility without any adverse reactions. On‐demand, selective control of dissolution behaviors with an animal model demonstrates an effective triggering strategy to program the system's lifetime, providing the possibility of potential applications in envisioned areas such as bioresorbable electronic implants and drug release systems.     

Ultrathin Hydrogel Films toward Breathable Skin-Integrated Electronics

On-skin electronics that offer revolutionary capabilities in personalized diagnosis, therapeutics, and human–machine interfaces require seamless integration between the skin and electronics. A common question remains whether an ideal interface can be introduced to directly bridge thin-film electronics with the soft skin, allowing the skin to breathe freely and the skin-integrated electronics to function stably. Here, an ever-thinnest hydrogel is reported that is compliant to the glyphic lines and subtle minutiae on the skin without forming air gaps, produced by a facile cold-lamination method. The hydrogels exhibit high water-vapor permeability, allowing nearly unimpeded transepidermal water loss and free breathing of the skin underneath. Hydrogel-interfaced flexible (opto)electronics without causing skin irritation or accelerated device performance deterioration are demonstrated. The long-term applicability is recorded for over one week. With combined features of extreme mechanical compliance, high permeability, and biocompatibility, the ultrathin hydrogel interface promotes the general applicability of skin-integrated electronics.     

Large‐Scale Direct‐Writing of Aligned Nanofibers for Flexible Electronics

Nanofibers/nanowires usually exhibit exceptionally low flexural rigidities and remarkable tolerance against mechanical bending, showing superior advantages in flexible electronics applications. Electrospinning is regarded as a powerful process for this 1D nanostructure; however, it can only be able to produce chaotic fibers that are incompatible with the well‐patterned microstructures in flexible electronics. Electro‐hydrodynamic (EHD) direct‐writing technology enables large‐scale deposition of highly aligned nanofibers in an additive, noncontact, real‐time adjustment, and individual control manner on rigid or flexible, planar or curved substrates, making it rather attractive in the fabrication of flexible electronics. In this Review, the ground‐breaking research progress in the field of EHD direct‐writing technology is summarized, including a brief chronology of EHD direct‐writing techniques, basic principles and alignment strategies, and applications in flexible electronics. Finally, future prospects are suggested to advance flexible electronics based on orderly arranged EHD direct‐written fibers. This technology overcomes the limitations of the resolution of fabrication and viscosity of ink of conventional inkjet printing, and represents major advances in manufacturing of flexible electronics.     

Molecularly inherent voltage-controlled conductance switching

Molecular electronics has been proposed as a pathway for high-density nanoelectronic devices. This pathway involves the development of a molecular memory device based on reversible switching of a molecule between two conducting states in response to a trigger, such as an applied voltage. Here we demonstrate that voltage-triggered switching is indeed a molecular phenomenon by carrying out studies on the same molecule using three different experimental configurations-scanning tunnelling microscopy, crossed-wire junction, and magnetic-bead junction. We also demonstrate that voltage-triggered switching is distinctly different from stochastic switching, essentially a transient (time-dependent) phenomenon that is independent of the applied voltage.     

Biodegradable Natural Pectin‐Based Flexible Multilevel Resistive Switching Memory for Transient Electronics

Transient electronics that can physically vanish in solution can offer opportunities to address the ecological challenges for dealing with the rapidly growing electronic waste. As one important component, it is desirable that memory devices combined with the transient feature can also be developed as secrecy information storage systems besides the above advantage. Resistive switching (RS) memory is one of the most promising technologies for next‐generation memory. Herein, the biocompatible pectin extracted from natural orange peel is introduced to fabricate RS memory devices (Ag/pectin/indium tin oxides (ITO)), which exhibit excellent RS characteristics, such as forming free characteristic, low operating voltages (≈1.1 V), fast switching speed (<70 ns), long retention time (>10⁴ s), and multilevel RS behaviors. The device performance is not degraded after 10⁴ bending cycles, which will be beneficial for flexible memory applications. Additionally, instead of using acid solution, the Ag/pectin/ITO memory device can be dissolved rapidly in deionized water within 10 min thanks to the good solubility arising from ionization of its carboxylic groups, which shows promising application for green electronics. The present biocompatible memory devices based on natural pectin suggest promising material candidates toward enabling high‐density secure information storage systems applications, flexible electronics, and green electronics.     

Microfluidics for flexible electronics

Flexible electronics has extensively drawn attention in an extremely wide range of areas due to its unique advantages like portability, biocompatibility, wearability, and superior mechanical stability. Recently, microfluidic technology has been considered as an effective tool to fabricate flexible electronics because of its precise control and manipulation of fluids in microchannels. In this review, we provide a comprehensive and in-depth insight into flexible electronics from microfluidic technology, covering the basic elements as well as microfluidic fabrication of flexible electronics and various applications in biomedical engineering. Furthermore, an outlook for the future challenges and perspectives of the flexible electronics is proposed.     

A Transient Pseudo-Capacitor Using a Bioderived Ionic Liquid with Na Ions

A pseudo-capacitor with transient behavior is applied in implantable, disposable, and bioresorbable devices, incorporating an Na ion-doped bioderived ionic liquid, molybdenum trioxide (MoO₃)-covered molybdenum foil, and silk sheet as the electrolyte, electrode, and separator, respectively. Sodium lactate is dissolved in choline lactate as a source of Na ions. The Experimental results reveal that the Na ions are intercalated into the van der Waals gaps in MoO₃, and the pseudo-capacitor shows an areal capacitance (1.5 mF cm⁻²) that is three times larger than that without the Na ion. The fast ion diffusion of the electrolyte and the low resistance of the MoO₃ and Mo interface result in an equivalent series resistance of 96 Ω. A cycle test indicates that the pseudo-capacitor exhibited a high capacitance retention of 82.8% after 10 000 cycles. The transient behavior is confirmed by the dissolution of the pseudo-capacitor into phosphate-buffered saline solution after 101 days. Potential applications of transient pseudo-capacitors include electronics without the need for device retrieval after use, including smart agriculture, implantable, and wearable devices.     

Physically Transient Threshold Switching Device Based on Magnesium Oxide for Security Application

Transient memristors are prospective candidates for both secure memory systems and biointegrated electronics, which are capable to physically disappear at a programmed time with a triggered operation. However, the sneak current issue has been a considerable obstacle to achieve high‐density transient crossbar array of memristors. To solve this problem, it is necessary to develop a transient switch device to turn the memory device on and off controllably. Here, a dissolvable and flexible threshold switching (TS) device with a vertically crossed structure is introduced, which exhibits a high selectivity of 10⁷, steep turn‐on slope of <8 mV dec⁻¹, and fast ON/OFF switch speed within 50/25 ns. Triggered failure could be achieved after soaking the device in deionized water for 8 min at room temperature. Furthermore, a water‐assisted transfer printing method is used to fabricate flexible and transient TS device arrays for bioresorbable systems, in which none of any significant degradation is observed under a bending radius of 2 mm. Integrating the selector with a transient memristor is capable of 10⁷ Gb memory implementation, indicating that the transient TS device could provide great opportunities to achieve highly integrated transient memory arrays.