We demonstrate the design and fabrication of novel nanoarchitectures of MnO(2)/Mn/MnO(2) sandwich-like nanotube arrays for supercapacitors. The crystalline metal Mn layers in the MnO(2)/Mn/MnO(2) sandwich-like nanotubes uniquely serve as highly conductive cores to support the redox active two-double MnO(2) shells with a highly electrolytic accessible surface area and provide reliable electrical connections to MnO(2) shells. The maximum specific capacitances of 937 F/g at a scan rate of 5 mV/s by cyclic voltammetry (CV) and 955 F/g at a current density of 1.5 A/g by chronopotentiometry were achieved for the MnO(2)/Mn/MnO(2) sandwich-like nanotube arrays in solution of 1.0 M Na(2)SO(4). The hybrid MnO(2)/Mn/MnO(2) sandwich-like nanotube arrays exhibited an excellent rate capability with a high specific energy of 45 Wh/kg and specific power of 23 kW/kg and excellent long-term cycling stability (less 5% loss of the maximum specific capacitance after 3000 cycles). The high specific capacitance and charge-discharge rates offered by such MnO(2)/Mn/MnO(2) sandwich-like nanotube arrays make them promising candidates for supercapacitor electrodes, combining high-energy densities with high levels of power delivery.

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Lithium is the most attractive anode material for high-energy density rechargeable batteries, but its cycling is plagued by morphological irreversibility and dendrite growth that arise in part from its heterogeneous “native” solid electrolyte interphase (SEI). Enriching the SEI with lithium fluoride (LiF) has recently gained popularity to improve Li cyclability. However, the intrinsic function of LiF—whether chemical, mechanical, or kinetic in nature—remains unknown. Herein, we investigated the stability of LiF in model LiF-enriched SEIs that are either artificially preformed or derived from fluorinated electrolytes, and thus, the effect of the LiF source on Li electrode behavior. We discovered that the mechanical integrity of LiF is easily compromised during plating, making it intrinsically unable to protect Li. The ensuing in situ repair of the interface by electrolyte, either regenerating LiF or forming an extra elastomeric “outer layer,” is identified as the more critical determinant of Li electrode performance. Our findings present an updated and dynamic picture of the LiF-enriched SEI and demonstrate the need to carefully consider the combined role of ionic and electrolyte-derived layers in future design strategies.

Lithium-ion batteries connected in series are prone to be overdischarged. Overdischarge results in various side effects, such as capacity degradation and internal short circuit (ISCr). However, most of previous research on the overdischarge of a cell was terminated when the cell voltage dropped to 0 V, leaving the further impacts of overdischarge unclear. This paper investigates the entire overdischarge process of large-format lithium-ion batteries by discharging the cell to −100% state of charge (SOC). A significant voltage platform is observed at approximately −12% SOC, and ISCr is detected after the cell is overdischarged when passing the platform. The scanning electron microscopy (SEM) and X-ray diffraction (XRD) results indicate that the overdischarge-induced ISCr is caused by Cu deposition on electrodes, suggesting possible Cu collector dissolution at the voltage platform near −12% SOC. A prognostic/mechanistic model considering ISCr is used to evaluate the resistance of ISCr (RISCr), the value of which decreases sharply at the beginning of ISCr formation. Inducing the ISCr by overdischarge is effective and well controlled without any mechanical deformation or the use of a foreign substance.

Lithium (Li) anodes suffer numerous challenges arising from the chemically inhomogeneous nature of the native solid electrolyte interphase (SEI), which impedes smooth plating and leads to dendrite growth. In spite of much attention paid to engineering Li interfaces of late, there is still limited understanding of the desired chemical composition of an improved Li SEI. One major challenge has been a lack of empirical data on the structure-property-performance relations in individual SEI phases, and specifically those present at a metallic Li interface, where the chemical potential imposed by Li will yield different material properties than the bulk analogues typically invoked to understand SEI behavior. Herein, we report preparation of single-component SEIs of lithium oxide (Li2O) grown ex situ onto Li foils by controlled metal-gas reactions, generating 'deconstructed' model interfaces with nanoscale thickness (20-100 nm) similar to the native, yet more complex multiphasic SEI. The model Li|Li2O electrodes serve as a platform for further chemical and electrochemical characterization. In particular, electrochemical impedance spectroscopy, combined with interface modeling, is used to extract transport properties (ionic conductivity, diffusivity, charge carrier concentration and activation energy barriers) of Li|Li2O in symmetric cells with EC/DEC electrolyte. The Li2O SEI is further studied as a function of synthesis condition, revealing microstructural sensitivities that can be tuned to modulate transport behaviors. Finally, results are compared with single-phase Li|LiF interfaces synthesized herein and with the native SEI to isolate chemistry-and structure-specific differences.

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Polyaniline (PANI) nanotube arrays were facilely synthesized via electrochemical polymerization in the presence of ZnO nanorod arrays as sacrificial templates, and they were tested as promising flexible electrode materials for supercapacitor applications.

The morphologies and structures for the thin film of blend systems consisting of two asymmetric polystyrene-block-polybutadiene (SB) diblock copolymers induced by annealing in the vapor of different solvents, namely, cyclohexane, benzene, and heptane, which have different selectivity or preferential affinity for a certain block, were investigated by tapping mode atomic force microscopy (AFM) and transmission electron microscopy (TEM). The results revealed that even a slight preferential affinity of good solvent for one block would strongly alter the morphology of the blend thin film. An interesting structure of so-called “spheres-between-cylinders” (“sph-b-cyl”) was obtained when annealing the blend thin film with a weight fraction ratio of 50/50 of the two components in the saturated vapor of cyclohexane, which is a good solvent for PB and a (near) ϑ solvent for PS at 34.5 °C. The influence of the kinetic factors, such as the annealing time and vapor pressure of the solvent, together with the factors of the blend composition and the film thickness, on the morphology forming in the blend thin film systems was also investigated. Blending the block copolymers together with the solvent treatments is proved to be an effective way to control the structure and morphology of the thin films.