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1.
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. EP has been used to characterize LIBs; here, we demonstrate the first application of EP to any NIB material. The voltage versus sodiation fraction curves (voltage profiles) of hard carbon lack clear features, consisting only of a slope and a plateau, making it difficult to clarify the structural features of hard carbon that could optimize cell performance. We find additional features through EP that are masked in the voltage profiles. We fit lattice gas models of hard carbon sodiation to experimental EP and system enthalpy, obtaining: 1. a theoretical maximum capacity, 2. interlayer versus pore filled sodium with state of charge.  相似文献   
2.
暴露于硫酸盐环境中的混凝土输水管易遭受硫酸盐化学侵蚀,导致其耐久性退化、提前失效;而环境中硫酸根离子传输进入混凝土是其化学侵蚀的前提.为获得混凝土内硫酸根离子的扩散进程,首先基于Fick定律及质量守恒定律,建立饱和混凝土管内硫酸根离子的扩散-反应模型.其次,将扩散-反应模型的边界条件齐次化,建立其有限元控制方程.然后,开展硫酸钠溶液中水泥砂浆圆柱试件的腐蚀试验,测定试件不同深度处的硫酸根离子浓度,与模型计算结果对比,以验证模型.最后,开展数值模拟研究,分析混凝土输水管外表面、内外表面暴露于浓度恒定或振荡的硫酸盐溶液情况下管内硫酸根离子浓度的时空分布.  相似文献   
3.
土壤硝态氮反映土壤短期氮素供应水平,实时了解土壤硝态氮的含量为精准农业和农业面源污染防控提供支撑,因此,在线实时检测土壤硝态氮方法突破就显得十分迫切。土壤硝态氮中的硝酸根离子在土壤中的高水溶性和流动性为全固态硝酸根离子选择电极高敏感检测土壤中硝态氮提供了条件,固态硝态氮离子选择电极的离子选择膜反应硝酸根离子在被测溶液中的浓度。采用全固态硝酸根离子选择电极,且与温度电极和pH电极融合组成电极阵列对土壤饱和溶液中的硝态根离子进行检测。设计了高输入阻抗运算放大电路对电极信号进行采集,并通过微处理控制蠕动泵完成土壤硝态氮待测溶液连续流动测量及实时传输结果。实验结果表明,电极响应时间≤15 s,斜率-51.63 mV/decade,线性范围10-5-10-2.2 mol/L,最低检测限10-5.23 mol/L。相对标准差在0.78%-4.47%范围内,加标回收率均在90%-110%以内。与国家标准紫外可见分光光度法测试结果相比,相关系数(R2)为0.9952,为土壤硝态氮在现场检测奠定技术基础。  相似文献   
4.
Multivalent ion storage and aqueous electrochemical systems continue to build interest for energy application. The Zn-ion system with 2 electron transfer and an ideal metal anode is a strong candidate but is still at the early stage of development. Using both in situ near-edge (XANES) and X-ray absorption fine structure spectroscopy, EXAFS, a nanostructured cathode material, CaxV2O5-H2O (CVO), was probed at the V-K absorption edge. This operando study reveals the local electronic and geometric structure changes for CVO during galvanostatic cycling as the active material in an aqueous Zn-ion cell. The XANES data provides a fine resolution to track the evolution of the vanadium oxidative state and near-neighbor coordination sphere showing subtle shifts and delocalized charge. The Zn-ion influence on the V-K absorption edge is visualized using a difference technique called Δμ. Coupled with theoretical calculations and modelling, the extended region extracted local bonding information further confirms excellent electronic and structural reversibility of this vanadium oxide bronze in an aqueous Zn-ion electrochemical cell.  相似文献   
5.
Xinwen Ma 《中国物理 B》2022,31(9):93401-093401
The research progresses on the investigations of atomic structure and collision dynamics with highly charged ions based on the heavy ion storage rings and electron ion beam traps in recent 20 years are reviewed. The structure part covers test of quantum electrodynamics and electron correlation in strong Coulomb field studied through dielectronic recombination spectroscopy and VUV/x-ray spectroscopy. The collision dynamics part includes charge exchange dynamics in ion-atom collisions mainly in Bohr velocity region, ion-induced fragmentation mechanisms of molecules, hydrogen-bound and van de Waals bound clusters, interference, and phase information observed in ion-atom/molecule collisions. With this achievements, two aspects of theoretical studies related to low energy and relativistic energy collisions are presented. The applications of data relevant to key atomic processes like dielectronic recombination and charge exchanges involving highly charged ions are discussed. At the end of this review, some future prospects of research related to highly charged ions are proposed.  相似文献   
6.
Linear and nonlinear phenomena are investigated in toroidal ion temperature gradient (TITG)-driven pure drift mode. The model includes inhomogeneity in background magnetic field, ion temperature, and density. Finite Larmor radius effect is incorporated to understand the effect of low-frequency wave on ion dynamics. Electrons are assumed to follow nonthermal distribution, that is, kappa and Cairns distributions. Dispersion relation is obtained to analyse the linear behaviour of the TITG mode in the presence of non-Maxwellian electron distribution. In the nonlinear regime, exact solutions (soliton and shocks) are obtained (in dispersive and dissipative medium respectively) by using functional variable method to solve the nonlinear partial differential equation obtained for the system under consideration. Graphical illustrations are used to exhibit the characteristics of linear and nonlinear structures and their dependence on different physical parameters. It is observed that for TITG-driven pure drift mode, rarefactive solitons are formed for both thermal and nonthermal electron distributions. It is also observed that variation of electrons from standard thermal distribution affects the propagation characteristics of linear and nonlinear structures in TITG-driven modes. Results of our investigations will be helpful to understand the low-frequency waves in inhomogeneous plasmas in the presence of nonthermal electron distributions which are frequently observed by satellite missions and are also observed in laboratory plasmas.  相似文献   
7.
In this paper, the problem of large amplitude dust acoustic (DA) solitons has been addressed in a charge varying dusty plasma with ions following a Cairns-Gurevich distribution. Based on the orbit motion limited approach, the correct Cairns-Gurevich ion charging current is presented for the first time. The expression relating the variable dust charge to the plasma potential is given in terms of the Lambert function and we take advantage of this transcendental function to, carefully, analyse DA solitons in a charge varying dusty plasma with trapped nonthermal ions. Our results show that the spatial patterns of the variable charge solitary wave are significantly changed due to the presence of ion population modelled by the Cairns-Gurevich distribution. An addition of a small concentration of trapped nonthermal ions makes the solitary structure less spiky, grows the net negative charge residing on the dust grain surface, and contributes to the electron depletion. Finally, our investigation is extended to highlight the effect of the grain dust charge variation. We have shown that under certain conditions, the impact of dust charge fluctuation may furnish an alternate physical mechanism rasing anomalous dissipation, which becomes more strong and may predominate over the dispersion as the nonthermal character of ions following the Cairns-Gurevich distribution increases.  相似文献   
8.
Rechargeable Mg batteries (RMBs) are advantageous large-scale energy-storage devices because of the high abundance and high safety, but exploring high-performance cathodes remains the largest difficulty for their development. Compared with oxides and sulfides, selenides show better Mg-storage performance because the weaker interaction with the Mg2+ cation favors fast kinetics. Herein, nanorod-like FeSe2 was synthesized and investigated as a cathode for RMBs. Compared with microspheres and microparticles, nanorods exhibit higher capacity and better rate capability with a smaller particle size. The FeSe2 nanorods show a high capacity of 191 mAh g−1 at 50 mA g−1 and a good rate performance of 39 mAh g−1 at 1000 mA g−1. Ex situ characterizations demonstrate the Mg2+ intercalation mechanism for FeSe2, and a slight conversion reaction occurs on the surface of the particles. The capacity fading is mainly because of the dissolution of Fe2+, which is caused by the reaction between Fe2+ and Cl of the electrolyte during the charge process on the surface of the particles. The surface of FeSe2 is mainly selenium after long cycling, which may also dissolve in the electrolyte during cycling. The present work develops a new type of Mg2+ intercalation cathode for RMBs. More importantly, the fading mechanism revealed herein has considered the specificity of Mg battery electrolyte and would assist a better understanding of selenide cathodes for RMBs.  相似文献   
9.
Novel processes have recently been developed that provide for the enhancement of ozonation through combination with electrochemical treatments. These are processes that can be included among those defined as advanced oxidation processes as they proceed via electrogeneration of highly oxidizing radical species.These processes are generally carried out by sparging ozone in both divided and undivided electrochemical cells in order to promote its decomposition through different mechanisms, depending on the electrode materials adopted, and in some cases still debated.This mini review presents the most recent advances in the field of electrochemically assisted ozonation.In particular, the first section is focused on the process known as electroperoxone (EP) where the ozone decomposition is enhanced by the adoption of carbon-based cathodes, due to the electrogeneration of hydrogen peroxide, while the second section is focused on the process that implies ozonation in a cell adopting metal-based cathodes.  相似文献   
10.
Yuejun Ding 《中国物理 B》2022,31(6):68201-068201
Na-ion batteries (NIBs) are regarding as the optimum complement for Li-ion batteries along with the rapid development of stationary energy storage systems. In order to meet the commercial demands of cathodes for NIBs, O3-type Cu containing layered oxide Na0.90Cu0.22Fe0.30Mn0.48O2 with good comprehensive performance and low-cost element components is very promising for the practical use. However, only part of the Cu3+/Cu2+ redox couple participated in the redox reaction, thus impairing the specific capacity of the cathode materials. Herein, Mg2+-doped O3-Na0.90Mg0.08Cu0.22Fe0.30Mn0.40O2 layered oxide without Mn3+ was synthesized successfully, which exhibited improved reversible specific capacity of 118 mAh/g in the voltage range of 2.4-4.0 V at 0.2 C, corresponding to the intercalation/deintercalation of 0.47 Na+ (0.1 more than that of Na0.90Cu0.22Fe0.30Mn0.48O2). This work demonstrates an important strategy to obtain advanced layered oxide cathodes for NIBs.  相似文献   
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