Exceptionally Reversible Li-/Na-Ion Storage and Ultrastable Solid-Electrolyte Interphase in Layered GeP Anode.

In this study, we synthesize two layered and amorphous structures of germanium phosphide (GeP) and compare their electrochemical performances to better understand the role of layered, crystalline structures and their ability to control large volume expansions. We compare the results obtained with those of previous, conventional viewpoints addressing the effectiveness of amorphous phases in traditional anodes (Si, Ge, and Sn) to hinder electrode pulverization. By means of both comprehensive experimental characterizations and density functional theory calculations, we demonstrate that layered, crystalline GeP in a hybrid structure with multiwalled carbon nanotubes exhibits exceptionally good transport of electrons and electrolyte ions and tolerance to extensive volume changes and provides abundant reaction sites relative to an amorphous structure, resulting in a superior solid-electrolyte interphase layer and unprecedented initial Coulombic efficiencies in both Li-ion and Na-ion batteries.

Nanoscale Zirconium-Abundant Surface Layers on Lithium- and Manganese-Rich Layered Oxides for High-Rate Lithium-Ion Batteries.

Battery performance, such as the rate capability and cycle stability of lithium transition metal oxides, is strongly correlated with the surface properties of active particles. For lithium-rich layered oxides, transition metal segregation in the initial state and migration upon cycling leads to a significant structural rearrangement, which eventually degrades the electrode performance. Here, we show that a fine-tuning of surface chemistry on the particular crystal facet can facilitate ionic diffusion and thus improve the rate capability dramatically, delivering a specific capacity of ∼110 mAh g at 30C.

Reversible crystalline-amorphous phase transformation in Si nanosheets with lithi-/delithiation.

Silicon (Si) has a large theoretical capacity of 4200 mAhg and has great potential as a high-performance anode material for Li ion batteries (LIBs). Meanwhile, nanostructures can exploit the potential of Si and, accordingly, many zero-dimensional (0D) and one-dimensional (1D) Si nanostructures have been studied. Herein, we report on two-dimensional (2D) Si nanostructures, Si nanosheets (SiNSs), as anodes for LIBs.

Lithium intercalation mechanism into FeF·0.5HO as a highly stable composite cathode material.

The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF·0.5HO and reduced graphene oxide (RGO) is synthesized for use as a high-performance cathode in LIBs, where RGO provides high electrical conductivity to the composite material.

Enhanced performance of sulfur-infiltrated bimodal mesoporous carbon foam by chemical solution deposition as cathode materials for lithium sulfur batteries.

The porous carbon matrix is widely recognized to be a promising sulfur reservoir to improve the cycle life by suppressing the polysulfide dissolution in lithium sulfur batteries (LSB). Herein, we synthesized mesocellular carbon foam (MSUF-C) with bimodal mesopore (4 and 30 nm) and large pore volume (1.72 cm/g) using MSUF silica as a template and employed it as both the sulfur reservoir and the conductive agent in the sulfur cathode.

Critical Role of pH Evolution of Electrolyte in the Reaction Mechanism for Rechargeable Zinc Batteries.

The reaction mechanism of α-MnO having 2×2 tunnel structure with zinc ions in a zinc rechargeable battery, employing an aqueous zinc sulfate electrolyte, was investigated by in situ monitoring structural changes and water chemistry alterations during the reaction. Contrary to the conventional belief that zinc ions intercalate into the tunnels of α-MnO , we reveal that they actually precipitate in the form of layered zinc hydroxide sulfate (Zn (OH) (SO )⋅5 H O) on the α-MnO surface. This precipitation occurs because unstable trivalent manganese disproportionates and is dissolved in the electrolyte during the discharge process, resulting in a gradual increase in the pH value of the electrolyte.

Polythiophene-Wrapped Olivine NaFePO4 as a Cathode for Na-Ion Batteries.

The surface of olivine NaFePO4 was modified with polythiophene (PTh) to develop a high-performance cathode material for use in Na-ion batteries. The Rietveld refinement results of the prepared material reveal that PTh-coated NaFePO4 belongs to a space group of Pnma with lattice parameters of a = 10.40656 Å, b = 6.

Investigation of the Na Intercalation Mechanism into Nanosized V2O5/C Composite Cathode Material for Na-Ion Batteries.

There is a significant interest to develop high-performance and cost-effective electrode materials for next-generation sodium ion batteries. Herein, we report a facile synthesis method for nanosized V2O5/C composite cathodes and their electrochemical performance as well as energy storage mechanism. The composite exhibits a discharge capacity of 255 mAh g(-1) at a current density of 0.

Layered-Layered-Spinel Cathode Materials Prepared by a High-Energy Ball-Milling Process for Lithium-ion Batteries.

In this work, we report the electrochemical properties of 0.5Li2MnO3·0.25LiNi0.

Elucidating the intercalation mechanism of zinc ions into α-MnO2 for rechargeable zinc batteries.

The intercalation mechanism of zinc ions into 2 × 2 tunnels of an α-MnO2 cathode for rechargeable zinc batteries was revealed. It involves a series of single and two-phase reaction steps and produces buserite, a layered compound with an interlayer spacing of 11 Å as a discharge product.

Controlling the intercalation chemistry to design high-performance dual-salt hybrid rechargeable batteries.

We have conducted extensive theoretical and experimental investigations to unravel the origin of the electrochemical properties of hybrid Mg(2+)/Li(+) rechargeable batteries at the atomistic and macroscopic levels. By revealing the thermodynamics of Mg(2+) and Li(+) co-insertion into the Mo6S8 cathode host using density functional theory calculations, we show that there is a threshold Li(+) activity for the pristine Mo6S8 cathode to prefer lithiation instead of magnesiation. By precisely controlling the insertion chemistry using a dual-salt electrolyte, we have enabled ultrafast discharge of our battery by achieving 93.

Electrochemically-induced reversible transition from the tunneled to layered polymorphs of manganese dioxide.

Zn-ion batteries are emerging energy storage systems eligible for large-scale applications, such as electric vehicles. These batteries consist of totally environmentally-benign electrode materials and potentially manufactured very economically. Although Zn/α-MnO2 systems produce high energy densities of 225 Wh kg(-1), larger than those of conventional Mg-ion batteries, they show significant capacity fading during long-term cycling and suffer from poor performance at high current rates.

Investigating local degradation and thermal stability of charged nickel-based cathode materials through real-time electron microscopy.

In this work, we take advantage of in situ transmission electron microscopy (TEM) to investigate thermally induced decomposition of the surface of Li(x)Ni(0.8)Co(0.15)Al(0.

Mechanochemical synthesis of Li₂MnO₃ shell/LiMO₂ (M = Ni, Co, Mn) core-structured nanocomposites for lithium-ion batteries.

Core/shell-like nanostructured xLi2MnO3·(1-x)LiMO2 (M = Ni, Co, Mn) composite cathode materials are successfully synthesized through a simple solid-state reaction using a mechanochemical ball-milling process. The LiMO2 core is designed to have a high-content of Ni, which increases the specific capacity. The detrimental surface effects arising from the high Ni-content are countered by the Li2MnO3 shell, which stabilizes the nanoparticles.

Stabilization of oxygen-deficient structure for conducting Li4Ti5O12-δ by molybdenum doping in a reducing atmosphere.

Li4Ti5O12 (LTO) is recognized as being one of the most promising anode materials for high power Li ion batteries; however, its insulating nature is a major drawback. In recent years, a simple thermal treatment carried out in a reducing atmosphere has been shown to generate oxygen vacancies (VO) for increasing the electronic conductivity of this material. Such structural defects, however, lead to re-oxidization over time, causing serious deterioration in anode performance.

Free standing acetylene black mesh to capture dissolved polysulfide in lithium sulfur batteries.

Herein, we report a cheap and simple approach to solve the polysulfide dissolution problem in lithium sulfur batteries. It was interestingly revealed that a simple insertion of acetylene black mesh enabled us to obtain the capacity of 1491 mA h g(-1) at initial discharge and 1062 mA h g(-1) after 50 cycles.

Influence of vanadium doping on the electrochemical performance of nickel oxide in supercapacitors.

In this study, V-doped NiO materials were prepared by simple coprecipitation and thermal decomposition, and the effect of the vanadium content on the morphology, structural properties, electrochemical behavior, and cycling stability of NiO upon oxidation and reduction was analyzed for supercapacitor applications. The results show an improvement in the capacitive characteristics of the V-doped NiO, including increases in the specific capacitance after the addition of just 1.0, 2.

Effect of multilayer structure on cyclic performance of Si/Fe anode electrode in lithium-ion secondary batteries.

A buffer-strengthened Si/Fe multilayer film, consisting of amorphous silicon layers and polycrystalline Fe layers, is investigated as the anode for Li-ion batteries. This film can achieve a stable cycle-life performance with a high capacity. Decreasing the thickness of the Fe layer can lead to a higher capacity, which is related to the fast transport of the Li ion, but the cyclic performance deteriorates with repeated cycling.

Photoelectrochemical polymerization of thiophene on self-assembled RuL2(NCS)2/di(3-aminopropyl)viologen on indium thin oxide.

Polythiophene layers were formed on self-assembled monolayers (SAMs)/indium tin oxide (ITO) using photoelectrochemical polymerization. The SAMs on ITO was prepared using Ru(4,4'-dicarboxylic acid-2,2'-bipyridine)2(NCS)2 and di(3-aminopropyl)viologen. The photoelectrochemically polymerized polythiophene layers on SAMs/ITO were characterized using UV-vis.

Enhancement of photoconversion efficiency of ZnO nanorod-based dye-sensitized solar cells in presence of ZrO2 thin energy barrier.

In order to enhance the power conversion efficiency of ZnO nanorods-based dye-sensitized solar cells (DSSCs), ZrO2 thin energy barriers were formed on ZnO nanorods using a sol-gel method. In DSSCs, the short-circuit current was substantially increased, and the dark current was significantly reduced in the presence of the ZrO2 layer. Due to suppressed recombination in the presence of the ZrO2 layer, 81.

Enhanced photocurrent generation of binary self-assembled monolayers of di-(3-aminopropyl)-viologen and methylviologen on indium tin oxide.

The binary self-assembled monolayers (SAMs) of di-(3-aminopropyl)-viologen (DAPV) and methylviologen (MV) molecules on indium tin oxide (ITO) were prepared by dipping the DAPV SAMs/ITO substrates into MV solution. The DAPV-MV SAM films were characterized by UV-vis. absorption spectroscopy, Rutherford backscattering spectroscopy, and cyclic voltammetry.

Modification of ion permeability utilizing pH-dependent selective swelling of polyelectrolyte multilayer films.

The selective swelling behavior of polyelectrolyte multilayer (PEM) films prepared by layer-by-layer (L-b-L) assembly influences the ion-permeability in contrast to surface charge density of the films. The cation terminated polyethylene amine (PEI) and anion terminated polyacrylic acid (PAA) were dissolved in DI water, and the pH was adjusted to 10 and 4, respectively, exemplifies thick denser film with good layering structure. The layered polyelectrolyte films has selective swelling behavior at pH 4 (PEI) or pH 10 (PAA), influences the permeability of both Ru(NH3)6(2+) and Fe(CN)6(3-) rather than surface charge character or film charge density.

Reduced recombination and photodegradation processes of photoelectrochemical cell-based on CdSe nanofibers in the presence of PEDOT:PSS layers.

This paper reports the use of poly(3,4-ethylenedioxythiophen):poly(styrene sulfonate) (PEDOT: PSS) as a protective layer to reduce the photodegradation and recombination processes of CdSe nanofiber films. Due to reduced photodegradation and recombination processes of photoelectrochemical cell-based CdSe nanofiber films, the power conversion efficiency of CdSe nanofibers films was 1.81% in the presence of PEDOT:PSS layers under the 1.

Enhanced photocurrent in the RuL2(NCS)2/ di-(3-aminopropyl)-viologen/Au nanoparticles/ITO system: use of Au nanoparticles for retardation of the back electron transfer reaction.

This paper reports the use of Au nanoparticles (NPs) as electron transfer bridge layers to improve the photocurrent of viologen/Ru complex-based photoelectrochemical cells. The Ru complex/ viologen/Au NPs on electrodes were prepared using self-assembled monolayers. The cell system showed an excellent photocurrent of 25 nA/cm2 under the 1.

Heterojunction of hydrophobic poly(1,4-phenylenevinylene) and hydrophilic PEDOT:PSS on hydrophilic CdS nanoparticles.

Heterojunction of hydrophobic poly(1,4-phenylenevinylene) (PPV) on hydrophilic CdS nanoparticles was successfully prepared by the multi-layering of poly(p-xylene tetrahydrothiophenium chloride) (pre-PPV: precursor of PPV polymer) and poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT:PSS) in an aqueous solution followed by a thermal treatment. CdS nanoparticles thin films were prepared on tin-doped indium oxide (ITO) by a chemical-bath-deposition method. The CdS surface was hydrophilic with low water contact angle of 15 degrees.