A Force-Assisted Li−O2 Battery Based on Piezoelectric Catalysis and Band Bending of MoS2/Pd Cathode

The high overpotential caused by the slow kinetics of oxygen reduction (ORR) and oxygen evolution (OER) has greatly limited the practical application of lithium-oxygen (Li−O₂) batteries. The adoption of force-field-assisted system based on a newly developed piezocatalysis is promising in reducing the overpotential. Herein, a force-assisted Li−O₂ battery is first established by employing MoS₂/Pd nanocomposite cathode, in which the piezoelectric polarization as well as built-in electric field are formed in MoS₂ piezoelectric catalyst under ultrasound activation, leading to the continuously separated electrons and holes to enhance the ORR and OER kinetics. Moreover, the introduction of Pd can promote the electrons transfer and further inhibit the complexation of electron–hole pairs, contributing to enhanced catalytic activity in the decomposition/generation of discharge products, resulting in reduced discharge/charge overpotentials. Thus, the force-assisted MoS₂/Pd-based Li−O₂ battery is capable of adjusting the output and input energies by the assisted ultrasonic wave. An ultra-low charging platform of 2.86 V and a high discharging platform of 2.77 V are achieved. The proposed unique force-assisted strategy can also be applied to lithium carbon dioxide battery system through the effective reduction and separation of CO₂ and CO₃²⁻, providing significant insights in achieving efficient energy conversion for metal−air batteries.     

Luminescence study of Eu3+doped Li6Y(BO3)3 phosphor for solid‐state lighting

In this study, Li₆Y_1–xEu_x(BO₃)₃ phosphor was successfully synthesized using a modified solid‐state diffusion method. The Eu³⁺ ion concentration was varied at 0.05, 0.1, 0.2, 0.5 and 1 mol%. The phosphor was characterized for phase purity, morphology, luminescent properties and molecular transmission at room temperature. The XRD pattern suggests a result closely matching the standard JCPDS file (#80‐0843). The emission and excitation spectra were followed to discover the luminescence traits. The excitation spectra indicate that the current phosphor can be efficiently excited at 395 nm and at 466 nm (blue light) to give emission at 595 and 614 nm due to the ⁵D₀ → ⁷F_j transition of Eu³⁺ ions. Concentration quenching was observed at 0.5 mol% Eu³⁺ in the Li₆Y_1–xEu_x(BO₃)₃ host lattice. Strong red emission with CIE chromaticity coordinates of phosphor is x = 0.63 and y = 0.36 achieved with dominant red emission at 614 nm the ⁵D₀ → ⁷ F₂ electric dipole transition of Eu³⁺ ions. The novel Li₆Y_1–xEu_x(BO₃)₃ phosphor may be a suitable red‐emitting component for solid‐state lighting using double‐excited wavelengths, i.e. near‐UV at 395 nm and blue light at 466 nm. Copyright © 2015 John Wiley & Sons, Ltd.     

Ti‐Gradient Doping to Stabilize Layered Surface Structure for High Performance High‐Ni Oxide Cathode of Li‐Ion Battery

High‐Ni layered oxide cathodes are considered to be one of the most promising cathodes for high‐energy‐density lithium‐ion batteries due to their high capacity and low cost. However, surfice residues, such as NiO‐type rock‐salt phase and Li₂CO₃, are often formed at the particle surface due to the high reactivity of Ni³⁺, and inevitably result in an inferior electrochemical performance, hindering the practical application. Herein, unprecedentedly clean surfaces without any surfice residues are obtained in a representative LiNi_0.8Co_0.2O₂ cathode by Ti‐gradient doping. High‐resolution transmission electron microscopy (TEM) reveals that the particle surface is composed of a disordered layered phase (≈6 nm in thickness) with the same rhombohedra structure as its interior. The formation of this disordered layered phase at the particle surface is electrochemically favored. It leads to the highest rate capacity ever reported and a superior cycling stability. First‐principles calculations further confirm that the excellent electrochemical performance has roots in the excellent chemical/structural stability of such a disordered layered structure, mainly arising from the improved robustness of the oxygen framework by Ti doping. This strategy of constructing the disordered layered phase at the particle surface could be extended to other high‐Ni layered transition metal oxides, which will contribute to the enhancement of their electrochemical performance.     

Realizing Interfacial Electronic Interaction within ZnS Quantum Dots/N‐rGO Heterostructures for Efficient Li–CO2 Batteries

With high theoretical energy density, rechargeable metal–gas batteries (e.g., Li–CO₂ battery) are considered as one of the most promising energy storage devices. However, their practical applications are hindered by the sluggish reaction kinetics and discharge product accumulation during battery cycling. Currently, the solutions focus on exploration of new catalysts while the thorough understanding of their underlying mechanisms is often ignored. Herein, the interfacial electronic interaction within rationally designed catalysts, ZnS quantum dots/nitrogen‐doped reduced graphene oxide (ZnS QDs/N‐rGO) heterostructures, and their effects on transformation and deposition of discharge products in the Li–CO₂ battery are revealed. In this work, the interfacial interaction can both enhance the catalytic activities of ZnS QDs/N‐rGO heterostructures and induce the nucleation of discharge products to form a homogeneous Li₂CO₃/C film with excellent electronic transmission and high electrochemical activities. When the batteries cycle within a cutoff specific capacity of 1000 mAh g^?1 at a current density of 400 mA g^?1, the cycling performance of the Li–CO₂ battery using a ZnS QDs/N‐rGO cathode is over 3 and 9 times than those coupled with a ZnS nanosheets (NST)/N‐rGO cathode and a N‐rGO cathode, respectively. This work provides comprehensive understandings on designing catalysts for Li–CO₂ batteries as well as other rechargeable metal–gas batteries.     

The Chemical Constituents of Garctnia xishuanbannanensis Y. H. Li Native to China

Garcinia xishuanbannanensis Y. H. Li is a rare tree species belonging to the Guttiferae and endemic in Xishuangbanna District of Yunnan. From its stem-bark two polyisoprenyl benzophenones-xanthochymol and isoxanthochymol have been isolated. They were identified on the basis of physico-chemical properties and UV, IR, 1HNMR, 13CNMR and MS analysis. The test of antitumor and antibacteria properties of these two compounds in mam- mals will be reported subsequently.     

Unusual Activation of Cation Disordering by Li/Fe Rearrangement in Triplite LiFeSO4F

It is reported that cation disordering in triplite LiFeSO₄F can be activated by Li/Fe rearrangement that results from irreversible and nondestructive structural changes during the 1st charge/discharge cycle, especially during the charge. This rearrangement decreases the number of edge‐shared FeO₄F₂ connection environments, compared to the pristine material. With this activation, triplite LiFeSO₄F exhibits several unexpected electrochemical features in subsequent cycles; a decrease in open‐circuit voltage indicating the change in thermodynamic property, negligible volumetric change, enhanced Li diffusion, and facile phase transformation pathway. As a consequence, the cation‐disordered triplite LiFeSO₄F achieves superior rate capability up to ≈66 mA h g^?1 at 40 C rate (1.5 min discharge) and has excellent capacity retention for 500 cycles at 5 C charge/5 C discharge rate and for 1200 cycles at 2 C charge/2 C discharge rate. Therefore, triplite LiFeSO₄F can be one of the most promising electrode materials for Li ion batteries.     

Surface Engineering Strategies of Layered LiCoO2 Cathode Material to Realize High‐Energy and High‐Voltage Li‐Ion Cells

Battery industries and research groups are further investigating LiCoO₂ to unravel the capacity at high‐voltages (>4.3 vs Li). The research trends are towards the surface modification of the LiCoO₂ and stabilize it structurally and chemically. In this report, the recent progress in the surface‐coating materials i.e., single‐element, binary, and ternary hybrid‐materials etc. and their coating methods are illustrated. Further, the importance of evaluating the surface‐coated LiCoO₂ in the Li‐ion full‐cell is highlighted with our recent results. Mg,P‐coated LiCoO₂ full‐cells exhibit excellent thermal stability, high‐temperature cycle and room‐temperature rate capabilities with high energy‐density of ≈1.4 W h cc^?1 at 10 C and 4.35 V. Besides, pouch‐type full‐cells with high‐loading (18 mg cm^?2) electrodes of layered‐Li(Ni,Mn)O₂ ‐coated LiCoO₂ not only deliver prolonged cycle‐life at room and elevated‐temperatures but also high energy‐density of ≈2 W h cc^?1 after 100 cycles at 25 °C and 4.47 V (vs natural graphite). The post‐mortem analyses and experimental results suggest enhanced electrochemical performances are attributed to the mechanistic behaviour of hybrid surface‐coating layers that can mitigate undesirable side reactions and micro‐crack formations on the surface of LiCoO₂ at the adverse conditions. Hence, the surface‐engineering of electrode materials could be a viable path to achieve the high‐energy Li‐ion cells for future applications.     

Thalassomonhystera traesti n.sp., Eumonhystera andrassyi and three Monhystrella species (Monhysteridae: Nematoda) from Li River, China

A new Thalassomonhystera species, i.e. T. traesti n.sp., and a new subspecies, Monhystrella lepidura chinensis n. subsp., together with Eumonhystera andrassyi (Biró, 1969) Andrássy, 1981, Monhystrella macrura (de Man, 1880) Andrássy, 1981 and Monhystrella iranica Schiemer, 1965 are described from Li River at Guiling, China. Thalassomonhystera traesti n.sp. is characterised by a combination of the following characters: expanded lip region, large and anteriorly situated amphids, prominent inner labial sensilla, and slender spicules and tube-like gubernaculum in males. Monhystrella lepidura chinensis n. subsp. belongs to Monhystrella lepidura (Andrássy, 1963) Andrássy, 1968 but differs from the three hitherto described subspecies in its possession of a pharynx that posteriorly expands into a double bulb. Monhystrella macrura, M. iranica and Eumonhystera andrassyiare reported here for the first time from China.