3D Porous Cu-Composites for Stable Li-Metal Battery Anodes.

Lithium (Li) metal is a promising anode material for lithium-ion batteries (LIBs) because of its high theoretical specific capacity of 3860 mAh g-1 and the low potential of -3.04 V versus the standard hydrogen electrode (SHE). However, these anodes rely on repeated plating and stripping of Li, which leads to consumption of Li inventory and the growth of dendrites that can lead to self-discharge and safety issues. To address these issues, as well as problems related to the volume change of these anodes, a number of different porous conductive scaffolds have been reported to create high surface area electrode on which Li can be plated reliably. While impressive results have been reported in literature, current processes typically rely on either expensive or poorly scalable techniques. Herein, we report a scalable fabrication method to create robust 3D Cu anodes using a one-step electrodeposition process. The areal loading, pore structure, and electrode thickness can be tuned by changing the electrodeposition parameters, and we show how standard mechanical calendering provides a way to further optimize electrode volume, capacity, and cycling stability. Optimized electrodes achieve high Coulombic efficiencies (CEs) of 99% during 800 cycles in half cells at a current density of 0.5 mA cm-2 with a total capacity of 0.5 mAh cm-2. To the best of our knowledge, this is the highest value ever reported for a host for Li-metal anodes using lithium bis(trifluoromethanesulfonyl)imide LITFSI based electrolyte.

Spinodal Decomposition Method for Structuring Germanium-Carbon Li-Ion Battery Anodes.

To increase the energy density of lithium-ion batteries (LIBs), high-capacity anodes which alloy with Li ions at a low voltage against Li/Li+ have been actively pursued. So far, Si has been studied the most extensively because of its high specific capacity and cost efficiency; however, Ge is an interesting alternative. While the theoretical specific capacity of Ge (1600 mAh g-1) is only half that of Si, its density is more than twice as high (Ge, 5.3 g cm-3; Si, 2.33 g cm-3), and therefore the charge stored per volume is better than that of Si. In addition, Ge has a 400 times higher ionic diffusivity and 4 orders of magnitude higher electronic conductivity compared to Si. However, similarly to Si, Ge needs to be structured in order to manage stresses induced during lithiation and many reports have achieved sufficient areal loadings to be commercially viable. In this work, spinodal decomposition is used to make secondary particles of about 2 µm in diameter that consist of a mixture of ∼30 nm Ge nanoparticles embedded in a carbon matrix. The secondary structure of these germanium-carbon particles allows for specific capacities of over 1100 mAh g-1 and a capacity retention of 91.8% after 100 cycles. Finally, high packing densities of ∼1.67 g cm-3 are achieved in blended electrodes by creating a bimodal size distribution with natural graphite.

Photo-Enhanced Magnesium-Ion Capacitors Using Photoactive Electrodes.

Off-grid power sources are becoming increasingly important for applications ranging from autonomous sensor networks to fighting energy poverty. Interactions of light with certain classes of battery and capacitor materials have recently gained attention to enhance the rate performance or to even charge energy storage devices directly with light. Interestingly, these devices have the potential to reduce the volume and cost of autonomous power sources. Here, a light-enhanced magnesium (Mg)-ion capacitor is shown. The latter is interesting because of the large natural abundance of Mg and its ability to operate in low cost and non-flammable aqueous electrolytes. Photoelectrodes using a combination of vanadium dioxide and reduced graphene oxide can achieve capacitance enhancements of up to 56% under light exposure alongside a 21% higher energy density of 20.5 mAh kg-1 .

Spontaneous rupture of pyogenic liver abscess with subcapsular hemorrhage mimicking ruptured hepatocellular carcinoma: A case report.

RATIONALE: Spontaneous rupture of PLA (pyogenic liver abscess) is an extremely rare and life-threatening event. Ruptured PLA is very difficult to distinguish from malignant HCC (hepatocellular cancer) rupture or cholangiocarcinoma rupture on CT (computed tomography) scan. PATIENT CONCERNS: We describe the case of a 71-year-old man with fever, right upper abdominal pain, nausea with intermittent vomiting, and general fatigue. He had no medical or surgical history. DIAGNOSIS: CT scan showed a hypodense mass in right hepatic lobe and MRI (magnetic resonance imaging) revealed a heterogenous mass of ∼6 cm in segment VI of the liver and heterogenous fluid in the subcapsular region. We made a tentative diagnosis of HCC rupture with subcapsular hemorrhage based on these findings. INTERVENTION: After improving the patient's condition by administering empirical therapy consisting of intravenous antibiotics and fluids, we performed surgical exploration. Gross examination of the abdomen showed that almost the entire right hepatic lobe was hemorrhagic and affected by peritonitis. Therefore, we performed right hepatectomy. The intraoperative frozen biopsy revealed suspicious PLA with marked necrosis, neutrophil infiltration, and hemorrhagic rupture, although no malignant tissue or fungus was observed. The postoperative secondary pathology report confirmed the diagnosis of PLA with hemorrhagic rupture. OUTCOMES: The patient was discharged 13 days after the operation. Follow-up CT was performed 5 months after discharge and revealed no abnormal findings. LESSONS: A high index of suspicion is key to preventing misdiagnosis of ruptured PLA and improving prognosis. Furthermore, even if rupture of the PLA is initially localized, delayed peritonitis may occur during medical treatment. Therefore, vigilant monitoring is essential.

Revealing molecular-level surface redox sites of controllably oxidized black phosphorus nanosheets.

Bulk and two-dimensional black phosphorus are considered to be promising battery materials due to their high theoretical capacities of 2,600 mAh g-1. However, their rate and cycling capabilities are limited by the intrinsic (de-)alloying mechanism. Here, we demonstrate a unique surface redox molecular-level mechanism of P sites on oxidized black phosphorus nanosheets that are strongly coupled with graphene via strong interlayer bonding. These redox-active sites of the oxidized black phosphorus are confined at the amorphorized heterointerface, revealing truly reversible pseudocapacitance (99% of total stored charge at 2,000 mV s-1). Moreover, oxidized black-phosphorus-based electrodes exhibit a capacitance of 478 F g-1 (four times greater than black phosphorus) with a rate capability of ~72% (compared to 21.2% for black phosphorus) and retention of ~91% over 50,000 cycles. In situ spectroelectrochemical and theoretical analyses reveal a reversible change in the surface electronic structure and chemical environment of the surface-exposed P redox sites.

Surface functional groups of carbon nanotubes to manipulate capacitive behaviors.

The covalent functionalization of carbon nanotubes (CNTs) is a basic but important chemistry that can modify their physicochemical properties, resolve their poor dispersion capability, and improve their capacitance to enable their use as high-energy supercapacitors. However, the relationship between functional groups on the CNT surface and their capacitive characteristics has not yet been explored. Here, we demonstrate the influence of carboxylic, sulfonic, and amine groups tethered to CNTs (Cf-CNTs, Sf-CNTs, and Nf-CNTs, respectively) on capacitor performance in an organic electrolyte. The Cf-CNTs show the highest specific capacitance of 129.4 F g(-1), four-fold greater than 31.2 F g(-1) of pristine CNTs, but they reveal the lowest rate capability of 57%. In contrast, the Sf- and Nf-CNTs exhibit specific capacitances of 70.9 F g(-1) and 83.6 F g(-1), two-fold greater than that of pristine CNTs, along with a good rate capability greater than 80%. Despite their pseudocapacitive nature, all functionalized CNTs show a cyclic stability of more than 80% after 500 cycles due to the electrochemical stability of the functional groups. As demonstrated by spectroscopic analysis, the supercapacitive behaviors of the functionalized CNTs originate from specific interactions between functional groups and lithium ions and the alteration of the electronic structure arising from covalent functionalization.