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CORROSION SCIENCE · 2022 · IF 7.72

Corrosion behaviour and mechanism of Mo in Lithium molten salt with SO42- at 500 °C

Jin Huang,Jian Zhang,Tingting Luo,Ruxia Liu,QinQin Wei,Guoqiang Luo,Qiang Shen

Corrosion test of Mo in LiF-LiCl-LiBr salt with different SO 4 2 content have been studied. MoO 2 , Mo 3 S 4 and MoS 2 was formed after corrosion. The SO 4 2- will corrode the grain boundary of Mo and lead to the decomposition of large Mo grain. Moreover, the formation of different corrosion products will lead to significant changes in volume and destroy the stable oxide layer which could be protective. The Mo will be severely corroded in LiF-LiCl-LiBr molten salt with a higher content of SO 4 2- .

CAS / MDL: 7439-98-7
研究领域: 材料科学 · 化学工程
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ENERGY · 2018 · IF 4.968

Water adsorption on the coated aluminum sheets by composite materials (LiCl + LiBr)/silica gel

Akram Entezari,T.S. Ge,R.Z. Wang

The desiccants made by confined salt in a porous matrix (CSPM) were proposed in the 1990s. Profiting off of a high sorption capacity and a low regeneration temperature made this field very interesting research topic. In absorption refrigeration cycles , adopting multi salts has been investigated widely. LiCl and LiBr are known for their high water adsorption capacity . The combinations of these two salts might be a tool for an intentional modification of CSPMs too. In this study, different ratios of these two salts were impregnated into silica gel pores. The textural properties, water sorption isotherms, and kinetics were analyzed. Four mathematical models were applied for estimating dynamic sorption coefficients. SIM and LDF were well-fitted to describe kinetics. The results showed that impregnated salts molar ratios affect the sorption characteristics. Adding a small amount of LiBr to the LiCl composites intensifies the sorption capacity up to 5.5% while adding LiCl to LiBr decrease this parameter by 12.7%. Besides, a mathematical simulation was used to estimate their performance in a real desiccant cooling heat exchanger . For a standard cooling and dehumidification conditions, the simulation results showed that the binary salt composites might improve the dehumidification if a proper salts ratio was selected.

CAS / MDL: 7550-35-8 7447-41-8
研究领域: 化学工程 · 材料科学
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2020 · IF 2.888

Solid−liquid phase equilibria of the quinary system containing lithium, sodium, calcium, strontium and chloride ions at 273.15 K and 101.325 kPa

Xia Wang,Kaiyu Zhao,Yafei Guo,Lingzong Meng,Tianlong Deng,Dan Li

The solid–liquid phase equilibria of systems LiCl–NaCl–CaCl 2 –SrCl 2 –H 2 O and CaCl 2 –SrCl 2 –H 2 O at 273.15 K and 0.1 MPa were investigated with the isothermal equilibrium method. The solid–liquid equilibrium phase diagrams were constructed with the experimental solubilities. The phase diagram in the ternary system consists of one univariant solubility curve saturated with solid solution (Ca,Sr)Cl 2 ·6H 2 O, and one crystallization field of the solid solution. There are three invariant points, seven isothermal univariant curves, and five crystallization regions saturated with NaCl corresponding to (Ca,Sr)Cl 2 ·6H 2 O, SrCl 2 ·2H 2 O, LiCl·2H 2 O, CaCl 2 ·4H 2 O and LiCl·CaCl 2 ·5H 2 O in the dry-salt diagram of the quinary system. The areas of crystallization zones decrease according to the above order. The J (NaCl), J (H 2 O), refractive index and density of the solution gradually change regularly with the increasing of J (CaCl 2 ) in the solution. These results on phase diagrams of the quinary system can supply theoretical reference for lithium salts and strontium salts separation from calcium chloride type brine.

研究领域: 化学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Single LiCl-driven synthesis of heptazine-/triazine-based crystalline carbon nitride homojunction for enhanced solar hydrogen evolution

Zhengliang Zhao,Zhu Shu,Jun Zhou,Tiantian Li,Kai Wang,Jingyang Song

LiCl-based molten salts have been widely used to induce the polymerization of melamine-derived monomer or intermediate into triazine-based or heptazine-based crystalline carbon nitride . Nevertheless, the role of LiCl beyond lowering melting point has not been fully revealed, and pure LiCl was exclusively reported to induce the formation of triazine-based crystalline counterpart. Herein, we firstly found that single LiCl can promote the deep deamination of melon-based pristine carbon nitride (PCN) to heptazine-based crystalline counterpart. As a result, a heptazine-/triazine-based crystalline carbon nitride homojunction was in situ formed by single LiCl-induced deamination and phase transition of PCN. It exhibits a favorable photocatalytic H 2 evolution reaction rate 18.3 times higher than PCN, which benefits from the promoted charges separation between heptazine and triazine units in phase homojunction. This work emphasizes that single LiCl can realize diverse modulation of carbon nitride framework with advanced photocatalytic activity.

CAS / MDL: 7447-41-8 108-78-1
研究领域: 材料科学 · 化学工程 · 能源科学
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

Stretchable PEDOT:PSS/Li-TFSI/XSB Composite Films for Electromagnetic Interference Shielding

Xin Jiang,Junwei Zhou,Xinke Zhong,Zhaopeng Hu,Rongyan Hu,Yihu Song,Qiang Zheng

Electromagnetic interference (EMI) shielding materials with stretchability are important for developing wearable and flexible appliances. Herein, lithium bis(trifloromethanesulfonyl)imide (Li-TFSI)-doped poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and carboxylated styrene-butadiene rubber (XSB) latex are used to prepare stretchable EMI shielding composite films of 0.2 mm in thickness. In these films, the doped PEDOT:PSS nanoparticles form tenuous conductive pathways between the hexagonally packed latex particles, resulting in higher EMI shielding efficiency (EMI SE) compared with the films containing traditional dopant ethylene glycol. For the purpose of stretchable EMI shielding, the films containing 6 wt % PEDOT:PSS and 6 wt % Li-TFSI demonstrate EMI SE of 50 and 30 dB (12.4 GHz) at 0 and 100% strains, respectively, being the highest values among the reported shielding composites except for those using liquid metal as the filler. The investigation also provides a simple and environmentally friendly preparation method being highlighted for the development of lightweight stretchable EMI shielding materials for applications in flexible electronics in the near future.

CAS / MDL: 90076-65-6
研究领域: 材料科学 · 电子工程
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Targeted research on the single role of lithium Bis(oxalate)borate in the film-forming process through a novel lithium salt-free electrolyte system

Shiyou Li,Li Yang,Peng Wang,Zhaojuan Li,Wenbo Li,Haining Liu,Xiaoling Cui

A blank comparison group of lithium salt-free electrolyte system, replacing the lithium salt of electrolyte with a redox shuttle agent, is constructed to give targeted research on the single role of lithium bis(oxalate)borate (LiBOB) salt, especially of bis(oxalate)borate anions (BOB − ) in the film-forming process. By combining and comparing all available studies, such as attenuated total reflectance (IR-ATR), X-Ray photoelectron diffraction spectrum (XPS), electrochemical impedance spectrum (EIS), scanning electron microscopy (SEM) tests and quantum chemical calculation , the formation mechanism of the solid electrolyte interphase (SEI) film is proposed. Results reveal that the prior reduction of BOB − anions can postpone the reduction potential and hinder the decomposition rate of carbonate solvents, but promote the formation of a dense, conductive and effective SEI film. This work provides a novel way to investigate the film-forming mechanism and has guiding significance for revealing the effect of other kinds of lithium salts on the surface film formation.

研究领域: 电化学 · 材料科学
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JOURNAL OF MOLECULAR LIQUIDS · 2020 · IF 5.065

(Solid + liquid) phase equilibria in the quaternary systems LiCl–Li2SO4–MgCl2–MgSO4–H2O and KCl–K2SO4–MgCl2–MgSO4–H2O at 288.15 K

Rui-Zhi Cui

The experimental solubility of LiCl–Li 2 SO 4 –MgCl 2 –MgSO 4 –H 2 O and KCl–K 2 SO 4 –MgCl 2 –MgSO 4 –H 2 O systems was measured at 288.15 K. The corresponding stable phase diagrams and water content diagrams were plotted by experimental results. Double salt was formed in both two systems. There are six phase fields, nine univariant solution curves and four invariant points in the phase diagram of LiCl–Li 2 SO 4 –MgCl 2 –MgSO 4 –H 2 O system. And the diagram of another system has seven invariant points and eight crystallization regions. By using multiple linear regression method, parameter Ψ Li,Cl,SO4 and the solubility equilibrium constants of double salt KCl·MgSO 4 ·3H 2 O were obtained by solubility data fitting at 288.15 K. The equilibrium solubility of salts in above systems at the same temperature was predicted with Pitzer's electrolyte solution model and mathematical calculation software. The results indicate that the predicted data are in correspondence with experiments.

研究领域: 化学 · 材料科学
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2022 · IF 3.119

Solid–Liquid Phase Equilibria and Boron Species Distribution in the Quaternary System LiCl–LiBO2–Li2B4O7–H2O at T = 323.15 K and P = 0.1 MPa

Tao Zhang,Liwei Zhuang,Dan Li,Lingzong Meng,Tianlong Deng,Yafei Guo,Yong Ma

The solubilities of salts, refractive indices, and pH values of the equilibrium liquid phases in the quaternary system LiCl–LiBO2–Li2B4O7–H2O at 323.15 K were investigated by the isothermal dissolution method for the first time. The dry-salt diagram of the quaternary system consisted of one invariant point, three univariant curves and three crystallization fields corresponding to LiCl·H2O, LiBO2·2H2O, and Li2B4O7·3H2O. The solution refractive indices and pH values change regularly with the changing of concentration. Combining the equilibrium constants for different boron species, the distributions of six boron species in the mixed solution in the systems LiCl–LiBO2–H2O, LiBO2–Li2B4O7–H2O, and LiCl–Li2B4O7–LiBO2–H2O were calculated with the total boron concentration and pH values. The main boron species in the mixed solution of the quaternary system are B3O3(OH)4–, B4O5(OH)42–, B(OH)3, and B5O6(OH)4–. The boron species distributions are mainly affected by the pH values and the concentration of total boron and LiCl in the solution. The results of phase diagram and boron species distribution in the quaternary system can supply foundation data for separating lithium borate from brines.

研究领域: 化学 · 材料科学
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LANGMUIR · 2024 · IF 3.7

Surface Coating of NCM523 Cathode Electrodes by the Difunctional Block Copolymer/Lithium Salt Composites

Qiaoyun Wu,Zhuijun Xu,Ying Yu,Meilan Peng,Jie Gao,Lei Nie,Ya-Jun Cheng,Peter Müller-Buschbaum,Yonggao Xia

Nickel-rich layered oxide cathodes, such as LiNi0.5Co0.2Mn0.3O2 (NCM523), are prevalent in high-power batteries owing to their high energy density. However, these cathodes suffer from undesirable side reactions occurring at the cathode/liquid electrolyte interface, leading to inferior interface stability and poor cycle life. To address these issues, herein, an amphiphilic diblock copolymer poly(dimethylsiloxane)-block-poly(acrylic acid) (PDMS-b-PAA) along with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) is utilized for modifying the electrode surface. This modification causes a thin and stable cathode–electrolyte interface (CEI) on the surface of NCM523 particles, as evidenced by XPS, TEM, and EIS analysis. The introduction of this modified interface successfully suppresses the capacity fading of NCM523. After 200 cycles at a rate of 1.0 C, the capacity of the modified NCM523 cathode is 108.7 mAh g–1, with a capacity retention of 82.8%, while the control samples without the polymer modification display a capacity retention of 72.7%. These results outline the distinct advantage of electrode surface modification with diblock copolymers/LiTFSI for the stabilization of Ni-rich layered oxide cathodes.

研究领域: 材料科学 · 电化学 · 能源存储
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Efficient adsorption of NH3 on Li salts@ hyper-crosslinked polymers: Equilibrium, kinetic, and thermodynamic analysis

Kai Zong,Xiaojun Bao,Kejie Jiang,Mei Zhang,Dongshun Deng

Gaseous ammonia (NH 3 ) pollution is harmful to human health and the environment. Developing adsorbents with excellent performance are in demand for NH 3 capture and separation. In this work, hyper-crosslinked polymer (HCP) with abundant pore and suitable surface property was prepared by one-step cross-linking reaction and applied to support various Li salts. The as-obtained Li salts@ HCPs were systematically characterized and evaluated for NH 3 adsorption at different composition and experimental conditions. The preferred [email protected] displayed reversible and outstanding NH 3 adsorption capacity of 37.33 mmol/g at 25℃ and 1.0 bar. Furthermore, kinetic and thermodynamics analysis revealed that the weak chemisorption of NH 3 on [email protected] was mainly controlled by adsorption equilibrium on the inner surface. The adsorption mechanism was elucidated using spectroscopic analysis and DFT calculations. Present work could provide more understanding of the gas–solid adsorption behavior and offer guidance for designing advanced materials for NH 3 capture and separation.

研究领域: 材料科学 · 环境科学
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Science China-Chemistry · 2011 ·Vol. 55 ·期 3 ·352-358 · IF 0

Capacitive properties of low potential electro-polymerized polyfluorene and activated carbon composite electrode

Liu Wei,Sun MingLiang,Wang Wei,Song LingXia,Ge HongLun,Sun Miao,Zhang QingJie

Polyfluorene (PF) film has been successfully electropolymerized at lower potential (0.91 V vs. Ag/AgCl) in the mixed electrolyte of boron trifluoride diethyl etherate and trifluoroacetic acid. The PF film is characterized to have about 10 repeat units and no presence of ketonic defect site. UV-vis and photoluminescent spectral studies indicate that the PF film is blue light emitting. From cyclic voltammetry and galvanostatic charge-discharge tests in 1 M lithium perchlorate/acetonitrile electrolyte, the polyfluorene/activated carbon electrode shows a specific capacitance of 227.1 F g −1 (per active layer mass) and reversible redox reaction at the potential of 1.4 V in a three electrode configuration. An asymmetric electrochemical capacitor based on this composite electrode and activated carbon electrode exhibits a specific energy of 14.7 Wh kg −1 (per active layer mass). These results indicate that electrochemically prepared polyfluorene could be used as energy storage component for electrochemical application.

CAS / MDL: 109-63-7 7791-03-9
研究领域: 材料科学 · 电化学
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IONICS · 2018 ·Vol. 24 ·期 7 ·2147-2155 · IF 2.347

Regularities of ionic solvation and association of lithium difluoro(oxalate)borate in dimethyl carbonate and sulfolane solvent systems

Li Jian,Meng Pengyu,Zhou Hongming

Lithium difluoro(oxalate)borate (LiODFB) is acknowledged as a new type of electrolyte lithium salt with great potential for high-voltage lithium-ion batteries. Utilizing Raman spectroscopy, a conductivity tester, and a viscometer, this study concentrates on the solution structures and properties of LiODFB-solvent systems. The results demonstrated that in the sulfolane (SL) solvent, the main coordination form is among the Li + cation. The ODFB − anion and SL molecules form an ionic solvation as a contact ion pair (CIP). The content of free Li + cations is very considerable, which is beneficial to improve the solubility and conductivity of LiODFB in the SL solvent. In the dimethyl carbonate (DMC) solvent, the main coordination form is ionic association as an aggregate (AGG). In addition, the solvent can display the comprehensive superiority of the SL solvent and LiODFB salt when a high concentration is dissolved in the SL-DMC as a mixed solvent.

研究领域: 化学 · 材料科学
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