Although carbonaceous materials possess long cycle stability and high power density, their low-energy density greatly limits their applications. On the contrary, metal oxides are promising pseudocapacitive electrode materials for supercapacitors due to their high-energy density. Nevertheless, poor electrical conductivity of metal oxides constitutes a primary challenge that significantly limits their energy storage capacity. Here, an advanced integrated electrode for high-performance pseudocapacitors has been designed by growing N-doped-carbon-tubes/Au-nanoparticles-doped-MnO2 (NCTs/ANPDM) nanocomposite on carbon fabric. The excellent electrical conductivity and well-ordered tunnels of NCTs together with Au nanoparticles of the electrode cause low internal resistance, good ionic contact, and thus enhance redox reactions for high specific capacitance of pure MnO2 in aqueous electrolyte, even at high scan rates. A prototype solid-state thin-film symmetric supercapacitor (SSC) device based on NCTs/ANPDM exhibits large energy density (51 Wh/kg) and superior cycling performance (93% after 5000 cycles). In addition, the asymmetric supercapacitor (ASC) device assembled from NCTs/ANPDM and Fe2O3 nanorods demonstrates ultrafast charge/discharge (10 V/s), which is among the best reported for solid-state thin-film supercapacitors with both electrodes made of metal oxide electroactive materials. Moreover, its superior charge/discharge behavior is comparable to electrical double layer type supercapacitors. The ASC device also shows superior cycling performance (97% after 5000 cycles). The NCTs/ANPDM nanomaterial demonstrates great potential as a power source for energy storage devices.
In this work, we report the development of well-ordered hydrogenated CoMoO (H-CoMoO) and hydrogenated FeO (H-FeO) nanoplate arrays on 3D graphene foam (GF) and explore their practice application as binder-free electrodes in assembling flexible all-solid-state asymmetric supercapacitor (ASC) devices. Our results show that the monolithic 3D porous GF prepared by solution casting method using Ni foam template possesses large surface area, superior electrical conductivity, and sufficient surface functional groups, which not only facilitate in situ growth of CoMoO and FeO nanoplates but also contribute the double-layer capacitance of the resultant supercapacitor. The well-ordered pseudocapacitive metal oxide nanoplate arrays standing up on 3D GF scaffold can provide efficient space and shorten the length for electrolyte diffusion from the outer to the inner region of the electrode material for Faradaic energy storage. Furthermore, one of our major findings is that the introduction of oxygen vacancies in CoMoO and FeO nanoplates by hydrogenation treatment can increase their electronic conductivity as well as improve their donor density and surface properties, which gives rise to a substantially improved electrochemical performance. Benefiting from the synergistic contributions of different components in the nanohybrid electrode, the resultant flexible ASC device with GF/H-CoMoO as the positive electrode and GF/H-FeO as the negative electrode achieves a wide operation voltage of 1.5 V and a maximum volumetric specific capacitance of 3.6 F cm, which is two times larger than that of the Ni/GF/CoMoO//Ni/GF/FeO device (1.8 F cm), and the rate capability is up to 70% as the current density increases from 2 to 200 mA cm. Moreover, the Ni/GF/H-CoMoO//Ni/GF/H-FeO device also exhibits a high energy density of 1.13 mWh cm and a high power density of 150 mW cm, good mechanical flexibility with the decrease in capacitance of less than 4% after being bent inward to different angles and inward to 90° 200 times, and good cycling stability of 93.1% capacitance retention after 5000 cycles.
A bifunctional self-supported electrode for water splitting to achieve a dynamic balance between HER and OER constructed via a one-step direct thermal sulfidization of NF.
Stroke is one of most common causes of death and disability. Most of neuroprotective agents fail to rescue neurons from cerebral ischemic insults, mainly because of targeting downstream cascading events, such as excitotoxicity, oxidative and nitrosative stress, and inflammation, rather than improving hypoxia that initially occurs. Here, we report a near-infrared light (NIR)-driven nanophotosynthesis biosystem capable of generating oxygen and absorbing carbon dioxide, thus rescuing neurons from ischemia toward treating stroke. Through cerebral delivery of S. elongatus that spontaneously photosynthesize and upconversion nanoparticles (UCNPs), NIR with excellent tissue penetrating capability is converted to visible light by UCNPs to activate S. elongatus generating oxygen in vivo, enhancing angiogenesis, reducing infarction, and facilitating repair of brain tissues, thus improving neuronal function recovery. The combination of cell-biological, biochemical, and animal-level behavioral data provides compelling evidence demonstrating that this oxygen-generating biosystem through jointly utilizing microorganism and nanotechnology represents a novel approach to stroke treatment.
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