Fermi Pressure and Coulomb Repulsion Driven Rapid Hot Plasma Expansion in a van der Waals Heterostructure.

Transition metal dichalcogenide heterostructures provide a versatile platform to explore electronic and excitonic phases. As the excitation density exceeds the critical Mott density, interlayer excitons are ionized into an electron-hole plasma phase. The transport of the highly non-equilibrium plasma is relevant for high-power optoelectronic devices but has not been carefully investigated previously. Here, we employ spatially resolved pump-probe microscopy to investigate the spatial-temporal dynamics of interlayer excitons and hot-plasma phase in a MoSe2/WSe2 twisted bilayer. At the excitation density of ∼1014 cm-2, well exceeding the Mott density, we find a surprisingly rapid initial expansion of hot plasma to a few microns away from the excitation source within ∼0.2 ps. Microscopic theory reveals that this rapid expansion is mainly driven by Fermi pressure and Coulomb repulsion, while the hot carrier effect has only a minor effect in the plasma phase.

Electrochemical properties of lithium powder anode cell with gel polymer electrolyte and lithium trivanadate cathode.

A Li secondary cell composed of a Li powder anode with a gel polymer electrolyte (GPE) and a lithium trivanadate cathode was assembled, and its morphology and electrochemical properties were investigated. The cell had an initial charge/discharge capacity of about 190 mA h g(-1) at 0.1 C-rate, with 70% capacity retention over more than 30 cycles. The morphologies in the anode after Li deposition/dissolution were observed by scanning electron microscopy. The GPE soaked well into the porous Li powder electrode before curing, enveloping the Li powder. The cured GPE suppressed dendrite formation of the Li powder anode and increased its reactive surface area.

Mechanical and Biocompatibility Properties of Sintered Titanium Powder for Mimetic 3D-Printed Bone Scaffolds.

A composite comprising Ti and NaCl powders was sintered similar to a three-dimensional (3D)-printed patient-customized artificial bone scaffold. Additionally, a proper microstructure of the mimetic scaffold and the optimum processing parameters for its development were analyzed. The mechanical properties of the metal-based porous-structured framework used as an artificial bone scaffold were an optimum replacement for the human bone. Thus, it was confirmed that patient-customized scaffolds could be manufactured via 3D printing. The 3D-printed mimetic specimens were fabricated by a powder-sintering method using Ti for the metal parts, NaCl as the pore former, and polylactic acid as the biodegradable binder. Scanning electron microscopy (SEM) images showed that pores were formed homogeneously, while X-ray computed tomography confirmed that open pores were generated. The porosity and pore size distribution were measured using a mercury porosimeter, while the flexural strength and flexural elastic modulus were calculated using the three-point bending test. Based on these measurements, a pore-former content of 15 vol % optimized the density and flexural strength to 2.52 g cm-2 and 283 MPa, respectively, similar to those of the actual iliac bone. According to the 3D-printing production method, a selective laser-sintering process was applied for the fabrication of the mimetic specimen, and it was determined that the microstructure and properties similar to those of previous metal specimens could be achieved in the as-prepared specimen. Additionally, a decellularized extracellular matrix (dECM) was used to coat the surfaces and interiors of the specimens for evaluating their biocompatibilities. SEM image analysis indicated that the adipose-derived stem cells grew evenly inside the pores of the coated specimens, as compared with the bulky Ti specimens without the dECM coating. The doubling time at 65% was measured at 72, 75, and 83 h for specimens with pore-former contents of 5, 10, and 15 vol %, respectively. The doubling time without the pore former was 116 h. As compared with the specimens without the pore former (73 h), 15% of the dECM-coated specimens showed a doubling time of 64%, measured at 47 h.

Reconfigurable Dipole-Induced Resistive Switching of MoS2 Thin Layers on Nb:SrTiO3.

The controllable band gap and charge-trapping capability of MoS2 render it suitable for use in the fabrication of various electrical devices with high-k dielectric oxides. In this study, we investigated reconfigurable resistance states in a MoS2/Nb:SrTiO3 heterostructure by using conductive atomic force microscopy. Low-resistance and high-resistance states were observed in all MoS2 because of barrier height modification resulting from redistribution of charge and oxygen vacancies in the vicinity of interfaces. In a thin layer of the MoS2 film, the carrier density was high, and layer-dependent transport properties appeared because of the charge separation in MoS2. The hysteresis and switching voltage of the MoS2/Nb:SrTiO3 heterostructure could be varied by controlling the number of layers of MoS2.

Energy-Density Improvement in Li-Ion Rechargeable Batteries Based on LiCoO2 + LiV3O8 and Graphite + Li-Metal Hybrid Electrodes.

We developed a novel battery system consisting of a hybrid (LiCoO2 + LiV3O8) cathode in a cell with a hybrid (graphite + Li-metal) anode and compared it with currently used systems. The hybrid cathode was synthesized using various ratios of LiCoO2:LiV3O8, where the 80:20 wt% ratio yielded the best electrochemical performance. The graphite and Li-metal hybrid anode, the composition of which was calculated based on the amount of non-lithiated cathode material (LiV3O8), was used to synthesize a full cell. With the addition of LiV3O8, the discharge capacity of the LiCoO2 + LiV3O8 hybrid cathode increased from 142.03 to 182.88 mA h g-1 (a 28.76% improvement). The energy density of this cathode also increased significantly, from 545.96 to 629.24 W h kg-1 (a 15.21% improvement). The LiCoO2 + LiV3O8 hybrid cathode was characterized through X-ray diffraction analysis, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Its electrochemical performance was analyzed using a battery-testing system and electrochemical impedance spectroscopy. We expect that optimized synthesis conditions will enable the development of a novel battery system with an increase in energy density and discharge capacity.

Effect of Tungsten Nanolayer Coating on Si Electrode in Lithium-ion Battery.

Tungsten (W) was coated onto a silicon (Si) anode at the nanoscale via the physical vaporization deposition method (PVD) to enhance its electrochemical properties. The characteristics of the electrode were identified by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray analysis, and electron probe X-ray microanalysis. With the electrochemical property analysis, the first charge capacities of the W-coated and uncoated electrode cells were 2558 mAh g- 1 and 1912 mAh g- 1, respectively. By the 50th cycle, the capacity ratios were 61.1 and 25.5%, respectively. Morphology changes in the W-coated Si anode during cycling were observed using SEM and TEM, and electrochemical characteristics were examined through impedance analysis. Owing to its conductivity and mechanical properties from the atomic W layer coating through PVD, the electrode improved its cyclability and preserved its structure from volumetric demolition.

Virtual Out-of-Plane Piezoelectric Response in MoS2 Layers Controlled by Ferroelectric Polarization.

The MoS2 carrier distribution can be controlled with the use of a dielectric environment substrate. Ferroelectric thin films are used to investigate the electrical responses at the MoS2 layer. The MoS2/(111)-PbTiO3 vertical heterostructure is investigated, and the electrical responses, including piezoelectricity, are obtained using piezoresponse force microscopy. The piezoelectric response modifications obtained at the MoS2 layer on the ferroelectric thin films are a result of the depolarizing effect. In particular, the piezoelectricity enhancement is observed at the 19-layer MoS2 because of an induced dipole effect. By considering the polarization effects of ferroelectric thin films, the electrical responses at the MoS2 layers can be controlled, and the interfacial carrier distribution at the interface results in different electrical performances at the MoS2.

Electrochemical Behaviors of a Vapor-Phase Polymerized Conductive Polymer Coated on LiV3O8 in Li-Metal Rechargeable Batteries.

A new coating method called vapor-phase polymerization (VPP) is used to coat a conductive polymer on LiV3O8 (LVO) surfaces for the first time in lithium-metal secondary batteries to protect the interface layer and enhance the electrochemical properties of the cathode. The VPP method can be used to coat an appropriate amount of the polymer and homogeneously coat the LVO active material surfaces because of the use of vapor-phase monomers. The presence of the coating layer was confirmed by X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and transmission electron microscopy. Polymer coating of LVO by VPP results in enhanced cyclic stability and rate capability at various C-rates. At 0.2 C-rate, it has high specific capacities of 254.7 and 272.2 mA h g-1 in the first and second cycles, respectively. Further, the capacity retention is 94.6% from the 2nd cycle to the 100th cycle. The improved electrochemical performance is attributed to the homogeneously conductive polymer formed by VPP, which can improve the electrical conductivity of the active material and inhibit dissolution by preventing direct contact with the electrolyte.

Quasi-Solid-State Rechargeable Li-O2 Batteries with High Safety and Long Cycle Life at Room Temperature.

As interest in electric vehicles and mass energy storage systems continues to grow, Li-O2 batteries are attracting much attention as a candidate for next-generation energy storage systems owing to their high energy density. However, safety problems related to the use of lithium metal anodes have hampered the commercialization of Li-O2 batteries. Herein, we introduced a quasi-solid polymer electrolyte with excellent electrochemical, chemical, and thermal stabilities into Li-O2 batteries. The ion-conducting QSPE was prepared by gelling a polymer network matrix consisting of poly(ethylene glycol) methyl ether methacrylate, methacrylated tannic acid, lithium trifluoromethanesulfonate, and nanofumed silica with a small amount of liquid electrolyte. The quasi-solid-state Li-O2 cell consisted of a lithium powder anode, a quasi-solid polymer electrolyte, and a Pd3Co/multiwalled carbon nanotube cathode, which enhanced the electrochemical performance of the cell. This cell, which exhibited improved safety owing to the suppression of lithium dendrite growth, achieved a lifetime of 125 cycles at room temperature. These results show that the introduction of a quasi-solid electrolyte is a potentially new alternative for the commercialization of solid-state Li-O2 batteries.

Electrochemical Behavior of Li-Cu Composite Powder Electrodes in Lithium Metal Secondary Batteries.

A new type of Li-Cu composite powder electrode (Li-Cu CE) was fabricated via mechanical blending of Li and Cu powders. The new Li-Cu electrode is capable of replacing Li metal anodes in Li metal secondary battery (LMSB) systems without exhibiting typical intrinsic problems such as dendrite growth, volume change, and electrolyte depletion. Thus, Li-Cu CE cells can offer longer lives and very high capacities. The Li particles in Li-Cu CEs are surrounded by Cu particles and thus cannot form networks that extend throughout the electrode. Isolation of the Li powder enables the control of Li+ ion migration during deposition and dissolution. The Li-Cu CE can thus prevent problematic volume changes and dendrite growth on the anode during battery operation. Symmetric Li-Cu CE cells are stable for up to 200 cycles at a rate of 3 C, and the anode capacity is estimated to be 1158 mAh g-1 (Li+ ion usage of 30%). These results are thought to represent a largest anode capacity for Li-metal in LMSBs.

Dendrite Suppression by Synergistic Combination of Solid Polymer Electrolyte Crosslinked with Natural Terpenes and Lithium-Powder Anode for Lithium-Metal Batteries.

Lithium-metal anode has fundamental problems concerning formation and growth of lithium dendrites, which prevents practical applications of next generation of high-capacity lithium-metal batteries. The synergistic combination of solid polymer electrolyte (SPE) crosslinked with naturally occurring terpenes and lithium-powder anode is promising solution to resolve the dendrite issues by substituting conventional liquid electrolyte/separator and lithium-foil anode system. A series of SPEs based on polysiloxane crosslinked with natural terpenes are prepared by facile thiol-ene click reaction under mild condition and the structural effect of terpene crosslinkers on electrochemical properties is studied. Lithium powder with large surface area is prepared by droplet emulsion technique (DET) and used as anode material. The effect of the physical state of electrolyte (solid/liquid) and morphology of lithium-metal anode (powder/foil) on dendrite growth behavior is systematically studied. The synergistic combination of SPE and lithium-powder anode suggests an effective solution to suppress the dendrite growth owing to the formation of a stable solid-electrolyte interface (SEI) layer and delocalized current density.

Flexible, Freestanding, and Binder-free SnO(x)-ZnO/Carbon Nanofiber Composites for Lithium Ion Battery Anodes.

Here, we demonstrate the production of electrospun SnO(x)-ZnO polyacrylonitrile (PAN) nanofibers (NFs) that are flexible, freestanding, and binder-free. This NF fabric is flexible and thus can be readily tailored into a coin for further cell fabrication. These properties allow volume expansion of the oxide materials and provide shortened diffusion pathways for Li ions than those achieved using the nanoparticle approach. Amorphous SnO(x)-ZnO particles were uniformly dispersed in the carbon NF (CNF). The SnO(x)-ZnO CNFs with a Sn:Zn ratio of 3:1 exhibited a superior reversible capacity of 963 mA·h·g(-1) after 55 cycles at a current density of 100 mA·g(-1), which is three times higher than the capacity of graphite-based anodes. The amorphous NFs facilitated Li2O decomposition, thereby enhancing the reversible capacity. ZnO prevented the aggregation of Sn, which, in turn, conferred stable and high discharge capacity to the cell. Overall, the SnO(x)-ZnO CNFs were shown to exhibit remarkably high capacity retention and high reversible and rate capacities as Li ion battery anodes.

Solid Polymer Electrolytes Based on Functionalized Tannic Acids from Natural Resources for All-Solid-State Lithium-Ion Batteries.

Solid polymer electrolytes (SPEs) for all-solid-state lithium-ion batteries are prepared by simple one-pot polymerization induced by ultraviolet (UV) light using poly(ethylene glycol) methyl ether methacrylate (PEGMA) as an ion-conducting monomeric unit and tannic acid (TA)-based crosslinking agent and plasticizer. The crosslinking agent and plasticizer based on natural resources are obtained from the reaction of TA with glycidyl methacrylate and glycidyl poly(ethylene glycol), respectively. Dimensionally stable free-standing SPE having a large ionic conductivity of 5.6×10(-4)  Scm(-1) at room temperature can be obtained by the polymerization of PEGMA into P(PEGMA) with a very small amount (0.1 wt %) of the crosslinking agent and 2.0 wt % of the plasticizer. The ionic conductivity value of SPE with a crosslinked structure is one order of magnitude larger than that of linear P(PEGMA) in the waxy state.

Preventing the dissolution of lithium polysulfides in lithium-sulfur cells by using Nafion-coated cathodes.

The principal drawback of lithium-sulfur batteries is the dissolution of long-chain lithium polysulfides into the electrolyte, which limits cycling performance. To overcome this problem, we focused on the development of a novel cathode as well as anode material and designed Nafion-coated NiCrAl/S as a cathode and lithium powder as an anode. Nafion-coated NiCrAl/S cathode was synthesized using a two-step dip-coating technique. The lithium-powder anode was used instead of a lithium-foil anode to prohibit dendrite growth and to improve on the electrochemical behaviors. The cells showed an initial discharge capacity of about 900 mA g(-1) and a final discharge capacity of 772 mA g(-1) after 100 cycles at 0.1 C-rate. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) demonstrate that using the Nafion-coated NiCrAl/S cathode can suppress the dissolution of long-chain lithium polysulfides.

Electrochemical analysis of the effect of Cr coating the LiV3O8 cathode in a lithium ion battery with a lithium powder anode.

Rechargeable 2032-coin-type cells were produced with Li-powder anodes (i.e., Li-powder electrodes, LPEs) and either Cr-coated lithium trivanadate (Li1+xV3O8, LVO) cathodes or uncoated LVO cathodes. The initial discharge capacity of a cell with an LPE and a Cr-coated LVO cathode (Cellcoated) was 252 mAh g(-1) at a 0.2 C-rate and that of a cell with an LPE and an uncoated LVO cathode (Cellbare) was 223 mAh g(-1). After the 50th cycle, Cellcoated exhibited higher capacity retention (about 89%) than Cellbare (about 78%). Changes in the surface morphology of the Cr-coated LVO cathode were observed using scanning electron microscopy and energy-dispersive X-ray spectroscopy. The change in the electrical conductivity of the cell was measured using the impedance analysis. The electrochemical properties of the cells were also evaluated based on the differential capacity curve, voltage profiles, and capacity versus number of cycles.