Attenuating the Polysulfide Shuttle Mechanism by Separator Coating.

Lithium-sulfur batteries have a high energy density but lack cycle stability to reach market maturity. This is mainly due to the polysulfide shuttle mechanism, i. e.

Synergistic effect of p-type and n-type dopants in semiconductors for efficient electrocatalytic water splitting.

The main challenge for acidic water electrolysis is the lack of active and stable oxygen evolution catalysts based on abundant materials, which are globally scalable. Iridium oxide is the only material which is active and stable. However, Ir is extremely rare.

Sodiation Of Hard Carbon: How Separating Enthalpy And Entropy Contributions Can Find Transitions Hidden In The Voltage Profile.

Sodium-ion batteries (NIBs) utilize cheaper materials than lithium-ion batteries (LIBs) and can thus be used in larger scale applications. The preferred anode material is hard carbon, because sodium cannot be inserted into graphite. We apply experimental entropy profiling (EP), where the cell temperature is changed under open circuit conditions.

Interface Phenomena.

This special collection on Interface Phenomena is dedicated to R. Jürgen Behm on the occasion of his retirement and 70th birthday. Jürgen Behm's research over the past 40 years has addressed a wide variety of interface processes in the fields of growth, corrosion, heterogeneous catalysis, electrocatalysis, and batteries.

Voltammetric Behaviour of LMO at the Nanoscale: A Map of Reversibility and Diffusional Limitations.

Understanding and optimizing single particle rate behaviour is normally challenging in composite commercial lithium-ion electrode materials. In this regard, recent experimental research has addressed the electrochemical Li-ion intercalation in individual nanosized particles. Here, we present a thorough theoretical analysis of the Li intercalation voltammetric behaviour in single nano/micro-scale LiMn O (LMO) particles, incorporating realistic interactions between inserted ions.

Quantifying structure dependent responses in Li-ion cells with excess Li spinel cathodes: matching voltage and entropy profiles through mean field models.

Measurements of the open circuit voltage of Li-ion cells have been extensively used as a non-destructive characterisation tool. Another technique based on entropy change measurements has also been applied for this purpose. More recently, both techniques have been used to make qualitative statements about aging in Li-ion cells.

Hierarchically porous three-dimensional electrodes of CoMoO₄ and ZnCo₂O₄ and their high anode performance for lithium ion batteries.

Ternary metal oxides have been receiving wide attention in electrochemical energy storage due to their rich redox reactions and tuneable conductivity. We present a simple solution-based method to prepare a 3D interconnected porous network of ternary metal oxide (CoMoO₄ and ZnCo₂O₄) nanostructures on macroporous nickel foam. The open-structured networks with different degrees of porosity endow them with high surface areas of electro-active sites.

Sodium vanadium oxide: a new material for high-performance symmetric sodium-ion batteries.

Room-temperature sodium-ion batteries have the potential to become the technology of choice for large-scale electrochemical energy storage because of the high sodium abundance and low costs. However, not many materials meet the performance requirements for practical applications. Here, we report a novel sodium-ion battery electrode material, Na(2.

Layered NaxMnO₂+z in sodium ion batteries-influence of morphology on cycle performance.

Due to its potential cost advantage, sodium ion batteries could become a commercial alternative to lithium ion batteries. One promising cathode material for this type of battery is layered sodium manganese oxide. In this investigation we report on the influence of morphology on cycle performance for the layered NaxMnO2+z.

Bulk antimony sulfide with excellent cycle stability as next-generation anode for lithium-ion batteries.

Nanomaterials as anode for lithium-ion batteries (LIB) have gained widespread interest in the research community. However, scaling up and processibility are bottlenecks to further commercialization of these materials. Here, we report that bulk antimony sulfide with a size of 10-20 μm exhibits a high capacity and stable cycling of 800 mAh g(-1).

History effects in lithium-oxygen batteries: how initial seeding influences the discharge capacity.

In laboratory experiments, Li-O2 systems show "sudden death" at capacities far below the theoretical value. Identifying how discharge products limit the total capacity is crucial in Li-O2 system. We investigated the effect of Li2O2 seed layer deposited on carbon cathode under potentiostatic conditions at increasing overpotentials to the subsequent slow discharge at galvanostatic condition.

Iron(III) sulfate: a stable, cost effective electrode material for sodium ion batteries.

Iron(iii) sulfate, a rhombohedral NASICON compound, has been demonstrated as a sodium intercalation host. This cost-effective material is attractive, as it can be slurry processed in bulk with ball-milling, while utilizing the iron 2(+)/3(+) redox couple, offering stable 3.2 V performance for over 400 cycles.

Building 3D structures of vanadium pentoxide nanosheets and application as electrodes in supercapacitors.

Various two-dimensional (2D) materials have recently attracted great attention owing to their unique properties and wide application potential in electronics, catalysis, energy storage, and conversion. However, large-scale production of ultrathin sheets and functional nanosheets remains a scientific and engineering challenge. Here we demonstrate an efficient approach for large-scale production of V2O5 nanosheets having a thickness of 4 nm and utilization as building blocks for constructing 3D architectures via a freeze-drying process.

Cu doped V2O5 flowers as cathode material for high-performance lithium ion batteries.

Hierarchical Cu doped vanadium pentoxide (V2O5) flowers were prepared via a simple hydrothermal approach followed by an annealing process. The flower precursors are self-assembled with 1D nanobelts surrounding a central core. The morphological evolution is investigated and a plausible mechanism is proposed.

Facile preparation of ordered porous graphene-metal oxide@C binder-free electrodes with high Li storage performance.

A facile and general method is reported to prepare ordered porous graphene-based binder-free electrodes on a large scale. This preparation process allows the easy adjustment of the selected components, weight ratio of componets, and the thickness of the electrodes. Such ordered porous electrodes demonstrate superior Li storage properties; for example, graphene-Fe3 O4 @C depicts high capacities of 1123.

Synthesis of cobalt phosphides and their application as anodes for lithium ion batteries.

A facile thermal decomposing method has been developed for the fabrication of Co(x)P nanostructures with controlled size, phase, and shape (e.g., Co(2)P rod and spheres, CoP hollow and solid particles).

Synthesis of one-dimensional hierarchical NiO hollow nanostructures with enhanced supercapacitive performance.

One-dimensional hierarchical hollow nanostructures composed of NiO nanosheets are successfully synthesized through a facile carbon nanofiber directed solution method followed by a simple thermal annealing treatment. With the advantages of high electro-active surface area, carbon nanofiber supported robust structure and short ion and electron transport pathways, the hierarchical hybrid nanostructures deliver largely enhanced capacitance with excellent cycling stability when evaluated as electrode materials for supercapacitors. More specifically, a high capacitance of 642 F g(-1) is achieved when the charge-discharge current density is 3 A g(-1) and the total capacitance loss is only 5.

Stabilization of large adsorbates by rotational entropy: a time-resolved variable-temperature STM study.

Investigating the dynamics in an adlayer of the oligopyridine derivative 2-phenyl-4,6-bis(6-(pyridine-2-yl)-4-(pyridine-4-yl)pyridine-2-yl)pyrimidine (2,4'-BTP) on Ag(111) by fast scanning tunneling microscopy (video-STM), we found that rotating 2,4'-BTP adsorbates coexist in a two-dimensional (2D) liquid phase (β-phase) in a dynamic equilibrium with static adsorbate molecules. Furthermore, exchange between an ordered phase (α-phase) and β-phase leads to fluctuations of the domain boundary on a time scale of seconds. Quantitative evaluation of the temperature-dependent equilibrium between rotating and static adsorbates, evaluated from a large number of STM images, gains insight into energetic and entropic stabilization and underlines that the rotating adsorbate molecules are stabilized by an entropy contribution, which is compatible with that derived by using statistical mechanics.

The role of surface defects in large organic molecule adsorption: substrate configuration effects.

The role of the configuration of metal surface atoms in the interaction between individual large, planar organic molecules and a metal substrate was investigated by low-temperature scanning tunneling microscopy and density functional theory calculations, including a semi-empirical correction scheme to account for dispersion effects. As test case, we used the adsorption of the oligopyridine derivative 2-phenyl-4,6-bis(6-(pyridine-2-yl)-4-(pyridine-4-yl)pyridine-2-yl)pyrimidine (2,4'-BTP) on a stepped Ag(100) surface. Both experiment, via statistical evaluation of the adsorption site and orientation of 2,4'-BTP admolecules, and theory indicate distinct structural effects.

Formation, atomic distribution and mixing energy in two-dimensional Pd(x)Ag(1-x) surface alloys on Pd(111).

The formation and atom distribution in two-dimensional Pd(x)Ag(1-x)/Pd(111) monolayer surface alloys were studied by high resolution scanning tunnelling microscopy (STM) with chemical contrast. From short-range order (SRO) parameters, we calculate preferences for like or unlike nearest neighbours to elucidate the mixing behaviour of the two components for various sub monolayer Ag surface contents. In the regime of low Ag surface contents (<40% Ag), the system shows a weak tendency towards phase separation, high Ag coverages (>60% Ag) result in a disperse distribution of the atoms in the surface.

Formation of ZnMn2O4 ball-in-ball hollow microspheres as a high-performance anode for lithium-ion batteries.

Novel ZnMn(2)O(4) ball-in-ball hollow microspheres are fabricated by a facile two-step method involving the solution synthesis of ZnMn-glycolate hollow microspheres and subsequent thermal annealing in air. When evaluated as an anode material for lithium-ion batteries, these ZnMn(2)O(4) ball-in-ball hollow microspheres show significantly enhanced electrochemical performance with high capacity, excellent cycling stability and good rate capability.

Oxidation of an organic adlayer: a bird's eye view.

The reaction of O(2) with an adlayer of the oligopyridine 2-phenyl-4,6-bis(6-(pyridine-2-yl)-4-(pyridine-4-yl)-pyridine-2-yl)pyrimidine (2,4'-BTP), adsorbed on the (111) surfaces of silver and gold and on HOPG--which can be considered as a model system for inorganic|organic contacts--was investigated by fast scanning tunneling microscopy (video STM) and dispersion corrected density functional theory (DFT-D) calculations. Only on Ag(111), oxidation of the 2,4'-BTP adlayer was observed, which is related to the fact that under the experimental conditions O(2) adsorbs dissociatively on this surface leading to reactive O adatoms, but not on Au(111) or HOPG . There is a distinct regiospecifity of the oxidation reaction caused by intermolecular interactions.

Intermolecular vs molecule-substrate interactions: A combined STM and theoretical study of supramolecular phases on graphene/Ru(0001).

The competition between intermolecular interactions and long-range lateral variations in the substrate-adsorbate interaction was studied by scanning tunnelling microscopy (STM) and force field based calculations, by comparing the phase formation of (sub-) monolayers of the organic molecules (i) 2-phenyl-4,6-bis(6-(pyridin-3-yl)-4-(pyridin-3-yl)pyridin-2-yl)pyrimidine (3,3'-BTP) and (ii) 3,4,9,10-perylene tetracarboxylic-dianhydride (PTCDA) on graphene/Ru(0001). For PTCDA adsorption, a 2D adlayer phase was formed, which extended over large areas, while for 3,3'-BTP adsorption linear or ring like structures were formed, which exclusively populated the areas between the maxima of the moiré structure of the buckled graphene layer. The consequences for the competing intermolecular interactions and corrugation in the adsorption potential are discussed and compared with the theoretical results.