Xiangya Wang

Abstract In recent years, the development of implantable bioelectronics has garnered significant attention. With the continuous advancement of IoT and information technology, implantable bioelectronics can be utilized more effectively for health monitoring to enhance treatment outcomes, reduce healthcare costs, and improve quality of life. Implantable energy storage devices have been widely studied as critical components for energy supply. Conventional power sources are bulky, inflexible, and potentially contain materials that are dangerous to the body. Meanwhile, human tissues are soft, flexible, dynamic, and closed, which puts new requirements on energy storage devices to improve the safety, stability, and matching of implantable batteries or supercapacitors. Herein, recent advances in state‐of‐the‐art nonconventional power options for implantable electronics, specifically biocompatible, miniaturized, stretchable/deformable, biodegradable/bioresorbable, edible, and injectable energy storage devices, are reviewed in this paper. The material strategy and architectural design of the next‐generation implantable energy storage device are discussed, including the selection principle of electrolytes, the all‐in‐one structure design strategy, and the way to realize self‐charging. Finally, the challenges and prospects of emerging design strategies toward developing next‐generation implantable batteries and supercapacitors for the future are put forward.

Abstract With the development of flexible and wearable electronic devices, it is a new challenge for polymer hydrogel electrolytes to combine high mechanical flexibility and electrochemical performance into one membrane. In general, the high content of water in hydrogel electrolyte membranes always leads to poor mechanical strength, and limits their applications in flexible energy storage devices. In this work, based on the “salting out” phenomenon in Hofmeister effect, a kind of gelatin‐based hydrogel electrolyte membrane is fabricated with high mechanical strength and ionic conductivity by soaking pre‐gelated gelatin hydrogel in 2 m ZnSO 4 aqueous. Among various gelatin‐based electrolyte membranes, the gelatin‐ZnSO 4 electrolyte membrane delivers the “salting out” property of Hofmeister effect, which improves both the mechanical strength and electrochemical performance of gelatin‐based electrolyte membranes. The breaking strength reaches 1.5 MPa. When applied to supercapacitors and zinc‐ion batteries, it can sustain over 7500 and 9300 cycles for repeated charging and discharging processes. This study provides a very simple and universal method to prepare polymer hydrogel electrolytes with high strength, toughness, and stability, and its applications in flexible energy storage devices provide a new idea for the construction of secure and stable flexible and wearable electronic devices.

In this study, thermoresponsive and mussel-inspired polypeptides were synthesized using ring-opening polymerization of α-amino acid derivatives of N-carboxyanhydride (NCA). The tissue adhesive properties of these polypeptides were evaluated using in vitro adhesive strength tests on porcine skin and bone. The results indicated that the species of the functional polypeptide side groups and the adhesive temperature have a significant influence on the adhesion strength. The maximum of the lap-shear adhesion strength on porcine skin was 101.2 kPa, and the maximum of tensile adhesion strength on bone was 603 kPa. The in vivo antibleeding activity and tissue adhesive ability were also evaluated using a rat model. These polypeptides exhibited superior hemostatic properties and healing effects in the skin incision and osteotomy gap, and the skin incision healing and osteotomy gap remodeling were completed in all rats after 2–9 weeks. These polypeptides are expected to be good candidates for surgical tissue adhesives, tissue engineering materials, and antibleeding materials, etc.

With the rapid advancement of implantable electronic medical devices, implantable supercapacitors have emerged as popular energy storage devices. However, supercapacitors inevitably come into direct contact with blood when implanted, potentially causing adverse clinical reactions such as coagulation and thrombosis, impairing the performance of implanted energy storage devices, and posing a serious threat to human health. Therefore, this work aims to design an anticoagulant supercapacitor by heparin doped poly(3, 4-ethylenedioxythiophene) (PEDOT) for possible applications in implantable bioelectronics. Heparin (Hep), the as-known anticoagulant macromolecule acts as the counterion for PEDOT doping to enhance its conductivity, and the bioelectrode material PEDOT: Hep with anticoagulant activity is synthesized via chemical oxidation polymerization. Concurrently, the anticoagulant supercapacitor is constructed through in-situ polymerization, where PEDOT: Hep and bacterial cellulose as electrode material and electrolyte layer, respectively. Owing to the incorporation of heparin, the supercapacitor exhibits high hemocompatibility with hemolysis rate <5 %, good anticoagulant performance with coagulation time of 63.4 s, reasonable cycle stability with capacitance retention rate of 76.24 % after 20, 000 cycles, and supplies power for implanted heart rate sensors in female mice. This work provides a platform for implantable electronics to achieve anticoagulant activity in vivo.