Flexible and safe batteries, coupled with high performance and low cost, constitute a radical advance in portable and wearable electronics, especially considering the fact that these flexible devices are likely to experience more mechanical impacts and potential damage than well-protected rigid batteries. However, flexible lithium ion batteries (LIBs) are vastly limited by their intrinsic safety and cost issues. Here we introduce an extremely safe and wearable solid-state zinc ion battery (ZIB) comprising a novel gelatin and PAM based hierarchical polymer electrolyte (HPE) and an α-MnO2 nanorod/carbon nanotube (CNT) cathode. Benefiting from the well-designed electrolyte and electrodes, the flexible solid-state ZIB delivers a high areal energy density and power density (6.18 mW h cm−2 and 148.2 mW cm−2, respectively), high specific capacity (306 mA h g−1) and excellent cycling stability (97% capacity retention after 1000 cycles at 2772 mA g−1). More importantly, the solid-state ZIB offers a high wearability and an extreme safety performance over conventional flexible LIBs, and performs very well under various severe conditions, such as being greatly cut, bent, hammered, punctured, sewed, washed in water or even put on fire. In addition, flexible ZIBs were integrated in series to power a commercial smart watch, a wearable pulse sensor, and a smart insole, which has been achieved to the best of our knowledge for the first time. These results demonstrate the promising potential of ZIBs in many practical wearable applications and offer a new platform for flexible and wearable energy storage technologies.
Over the past two decades, a series of aqueous rechargeable metal-ion batteries (ARMBs) have been developed, aiming at improving safety, environmental friendliness and cost-efficiency in fields of consumer electronics, electric vehicles and grid-scale energy storage. However, the notable gap between ARMBs and their organic counterparts in energy density directly hinders their practical applications, making it difficult to replace current widely-used organic lithium-ion batteries. Basically, this huge gap in energy density originates from cell voltage, as the narrow electrochemical stability window of aqueous electrolytes substantially confines the choice of electrode materials. This review highlights various ARMBs with focuses on their voltage characteristics and strategies that can effectively raise battery voltage. It begins with the discussion on the fundamental factor that limits the voltage of ARMBs, i.e., electrochemical stability window of aqueous electrolytes, which decides the maximum-allowed potential difference between cathode and anode. The following section introduces various ARMB systems and compares their voltage characteristics in midpoint voltage and plateau voltage, in relation to respective electrode materials. Subsequently, various strategies paving the way to high-voltage ARMBs are summarized, with corresponding advancements highlighted. The final section presents potential directions for further improvements and future perspectives of this thriving field.
The Zn/Co3O4 battery is one of the few aqueous electrolyte batteries with a potential >2 V voltage. Unfortunately, so far, all reported Zn/Co3O4 batteries are using an alkaline electrolyte, resulting in poor cycling stability and environmental problems. Here, we report a Co(III) rich-Co3O4 nanorod material with vastly improved electrochemical kinetics. Zn/Co(III) rich-Co3O4 batteries can work well in ZnSO4 with a CoSO4 additive aqueous solution as a mild electrolyte, delivering a high voltage of 2.2 V, a capacity of 205 mA h g−1 (Co3O4) and an extreme cycling stability of 92% capacity retention even after 5000 cycles. Further mechanistic study reveals a conversion reaction between in situ formed CoO and Co3O4, which has never been observed in an alkaline Zn/Co3O4 battery. Subsequently, a flexible solid-state battery is constructed and reveals high flexibility and a high energy density of 360.8 W h kg−1 at a current density of 0.5 A g−1. Our research initiates the first Zn/Co3O4 battery working in a mild electrolyte, resulting in excellent electrochemical performance. It also indicates that the electrochemical kinetics can be effectively enhanced by fine tuning the atomic structure of electrode materials, opening a new door to improve the performance of aqueous electrolyte batteries.
The flourishing development of multifunctional flexible electronics cannot leave the beneficial role of nature, which provides continuous inspiration in their material, structural, and functional designs. During the evolution of flexible electronics, some originated from nature, some were even beyond nature, and others were implantable or biodegradable eventually to nature. Therefore, the relationship between flexible electronics and nature is undoubtedly vital since harmony between nature and technology evolution would promote the sustainable development. Herein, materials selection and functionality design for flexible electronics that are mostly inspired from nature are first introduced with certain functionality even beyond nature. Then, frontier advances on flexible electronics including the main individual components (i.e., energy (the power source) and the sensor (the electric load)) are presented from nature, beyond nature, and to nature with the aim of enlightening the harmonious relationship between the modern electronics technology and nature. Finally, critical issues in next‐generation flexible electronics are discussed to provide possible solutions and new insights in prospective exploration directions.
30 January 2019 in ACS Applied Materials & Interfaces