Search for: All records

The growing demand for bioelectronics has generated widespread interest in implantable energy storage. These implantable bioelectronic devices, powered by a complementary battery/capacitor system, have faced difficulty in miniaturization without compromising their functionality. This paper reports on the development of a promising high‐rate cathode material for implantable power sources based on Li‐exchanged Na_1.5VOPO₄F_0.5anchored on reduced graphene oxide (LNVOPF‐rGO). LNVOPF is unique in that it offers dual charge storage mechanisms, which enable it to exhibit mixed battery/capacitor electrochemical behavior. In this work, electrochemical Li‐ion exchange of the LNVOPF structure is characterized by operando X‐ray diffraction. Through designed nanostructuring, the charge storage kinetics of LNVOPF are improved, as reflected in the stored capacity of 107 mAh g⁻¹at 20C. A practical full cell device composed of LNVOPF and T‐Nb₂O₅, which serves as a pseudocapacitive anode, is fabricated to demonstrate not only high energy/power density storage (100 Wh kg⁻¹at 4000 W kg⁻¹) but also reliable pulse capability and biocompatibility, a desirable combination for applications in biostimulating devices. This work underscores the potential of miniaturizing biomedical devices by replacing a conventional battery/capacitor couple with a single power source.

 

Over the course of more than three decades, Li-ion batteries have come to revolutionize the way we store and transport energy. These incredibly compact electrochemical devices rely fundamentally on the ability to reversibly insert lithium ions into densely packed arrangements of atoms. Of the tens of thousands of materials reported in the structural databases, only a very small number have been shown to be capable of accommodating the kind of fast ionic diffusion necessary to operate in practical devices. In honor of John B. Goodenough’s 100th birthday, this perspective will overview the current understanding of the kinds of structural features that help and/or hurt fast lithium ion transport through insertion hosts, with a particular focus on the role that the rotation of rigid subunits plays in the movement of lithium through the solid state.