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LiCl熔盐
CERAMICS INTERNATIONAL · 2020 · IF 3.83

Formation and growth of LaOCl:Eu3+ crystal in KCl-LiCl molten flux and its luminescent properties

Yuan-Pei Lan,Chaoyi Chen,Junqi Li,Xuewen Xia,Xisong Mao,Hao Zhou

Homogeneously Eu 3+ doped LaOCl single crystals are firstly synthesized in a molten KCl-LiCl flux, and the well-shaped LaOCl:Eu 3+ polyhedral micro-plates exhibit noticeable luminescent properties. The bulk LaOCl:Eu 3+ micro-plate with a width of 1.03 μm and 1.37 μm in length shows a single crystal characteristic with the crystal face orientation of [00 1 ‾ ]. Both XRD patterns and EDS mapping indicate that the Eu 3+ ions have been homogeneously doped into LaOCl lattice. LaOCl:Eu 3+ nucleuses generated in molten KCl-LiCl flux at even 350 °C benefited to the decomposition of La(OH) 3 :Eu 3+ precursor, and polyhedral LaOCl micro-plate is easily formed in molten KCl-LiCl salt due to the solid-ionic reaction and crystal growth. The luminescent properties of LaOCl:Eu 3+ are firstly enhanced and then weakened with the increasing concentration of the doped Eu 3+ , 6% Eu 3+ doped LaOCl:Eu 3+ exhibits the best luminescent properties which can be used as a potential LED material.

研究领域: 材料科学 · 光学
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2019 ·Vol. 166 ·期 8 ·D276 · IF 3.12

Preparation of γ-Uranium-Molybdenum Alloys by Electrochemical Reduction of Solid Oxides in LiCl Molten Salt

Yu-Ke Zhong,Kui Liu,Ya-Lan Liu,Yue-Xiang Lu,Tai-Qi Yin,Lin Wang,Zhi-fang Chai,Wei-Qun Shi

Uranium-molybdenum (U-Mo) alloys especially the γ-U-Mo phase, with excellent irradiation performance at high temperatures, have been extensively studied as low-enriched-uranium candidate fuels for strengthening nuclear security and nonproliferation worldwide. Herein, we provide a facile method to successfully prepare the γ-U-Mo alloys (U-10Mo and U-8Mo) directly from oxide precursors via electro-reduction by constant cell voltage electrolysis in LiCl molten salt at 986 K. The reduction mechanism was elucidated through cyclic voltammetry using the metallic cavity electrode (MCE) combined with XRD, SEM and EDS characterizations toward the electrolysis products under different conditions. It was found that the reduction of mixed MoO3-UO2 oxides may take place in three steps. Firstly, MoO3 was reduced to Li4Mo5O12, and then Li4Mo5O12 was converted into Mo. Finally, the U-Mo alloys were formed due to the underpotential deposition of U on the pre-formed Mo. In addition, the effects of cell voltage, sintering temperature and mixture composition on the electrochemical reduction were investigated. The results found that the reduction rate increased with the augmentation of applied potential and the decrease of sintering temperature. Moreover, the favorable composition of the mixed precursor varied from 24 at% to 21at%. The reduction conversion rate was determined to be 93.7% by ICP and TGA.

CAS / MDL: 7447-41-8
研究领域: 材料科学 · 核能工程
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

KCl–LiCl molten salt synthesis of LaOCl/CeO2-g-C3N4 with excellent photocatalytic-adsorbed removal performance for organic dye pollutant

Zhiyao Chu,Junqi Li,Yuan-Pei Lan,Chaoyi Chen,Jian Yang,Deyang Ning,Xuewen Xia,Xisong Mao

A ternary photocatalyst of LaOCl/CeO 2 -g-C 3 N 4 was designed and firstly synthesized by a facile KCl–LiCl molten salt method. The 60 %LaOCl/40 %CeO 2 -g-C 3 N 4 with a 6: 4 weight ratio of LaOCl to CeO 2 has an optimal degradation ratio (nearly 100%) for methylene blue (MB) with an impressive cyclic stability. Both of adsorption and photodegradation contribute to the high MB removal ratio, and kinetic study results show that the rate constant of photocatalytic degradation route is 0.0174 min −1 , which is less than that of adsorption process (2.4406 min −1 ). The excellent adsorption performance of 60 %LaOCl/40 %CeO 2 -g-C 3 N 4 is attributed to its negative zeta potential (−35.40 mV) and larger average pore size. The photochemical characterizations suggest that the 60 %LaOCl/40 %CeO 2 -g-C 3 N 4 form a dual Z-scheme heterojunction , which enhances its separation efficiency of photogenerated e - / h + with an outstanding redox ability, and further promotes the photocatalytic activity.

研究领域: 材料科学 · 环境科学
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JOURNAL OF NUCLEAR MATERIALS · 2022 · IF 3.555

Diffusion behavior of oxygen in the electro-deoxidation of uranium oxide in LiCl-rich melt

Benlin Yao,Yiqun Xiao,Yanhong Jia,Sida Wu,Mingshuai Yang,Hui He

The role of oxygen in the electrolytic reduction of uranium oxide in molten salt has received increased attention in recent years. In contrast to solubility, few studies were reported on the kinetic property of oxygen in LiCl. In this work, diffusion behaviors of oxygen anion in the bulk salt and oxide cathode were both studied. A gold working electrode was used to conduct corresponding voltammetry studies in LiCl-rich melt at 923 K. The obtained diffusion coefficient increased when another salt (KCl or LiF) was introduced to LiCl. A model based on ohmic, concentration and electrochemical polarizations was derived and used to describe the electro-deoxidation of uranium oxide in molten salt. By analyzing experimental current-time curves obtained from potentiostatic electrolysis, parameters such as exchange current density, conductivity of porous uranium filled with electrolyte and diffusion coefficient of oxygen anion in porous uranium were calculated. Taken together, the behavior of oxygen in the electro-deoxidation of uranium oxide in LiCl-rich melt can be better understood.

CAS / MDL: 12057-24-8 1313-99-1
研究领域: 材料科学 · 电化学 · 核工程
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Nanoscale · 2019 ·Vol. 11 ·期 26 ·12537-12546 · IF 6.97

High-efficiency transformation of amorphous carbon into graphite nanoflakes for stable aluminum-ion battery cathodes

Jiguo Tu,Junxiang Wang,Shijie Li,Wei-Li Song,Mingyong Wang,Hongmin Zhu,Shuqiang Jiao

Highly efficient strategies for the transformation of amorphous carbon into graphite with high graphitization and crystallinity features have been significantly pursued in recent years; however, critical issues, including high processing temperature, insufficient graphitization, introduction of catalyst impurities, complicated post-purification procedures, and generation of greenhouse gas, still remain in traditional approaches. For significantly addressing these challenges, herein, a highly efficient catalyst-free, eco-friendly and low-temperature electrochemical transformation strategy was proposed for the preparation of highly graphitized porous graphite nanoflakes. Using inert SnO2 as an anode in CaCl2-LiCl molten salts, the graphitization transformation of amorphous carbon materials could be realized at 700 °C, approaching the record in high-efficiency converting amorphous carbon to graphite; moreover, systematical analysis was performed to understand the electrochemical transformation of amorphous carbon into highly graphitized graphite nanoflakes. For extending their valuable applications, the as-prepared graphite nanoflakes were further utilized as cathodes in aluminum-ion batteries, which exhibited significantly promising energy storage performance; moreover, an initial discharge capacity of 63.6 mA h g−1 at a current density of 200 mA g−1 was achieved, which eventually became 55.5 mA h g−1 with a coulombic efficiency of 95.4% after 1000 cycles; thus, these cathodes exhibited stable long-term cycling performance. The combination of low-temperature electrochemical transformation and the subsequent high-performance applications of these nanoflakes in energy storage indicates that the proposed strategy is highly efficient for the transformation and utilization of abundant amorphous carbon resources for the realization of high value-added applications.

CAS / MDL: 65039-09-0
研究领域: 材料科学 · 电化学 · 能量存储 · 纳米技术
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY · 2023 ·Vol. 332 ·期 4 ·1353-1365 · IF 1.6

Electrochemical separation of fission element samarium on lead electrodes from KCl–LiCl molten salts and the kinetic research of the process

Wang Zhaoyang,Shen Yubo,Zhang Yinshan,Liu Yuhui,Dong Zhimin,Quan Meiyang,Yu Fengtao,Cao Xiaohong,Zhang Zhibin,Wang Yingcai,Liu Yunhai

In order to improve the utilization of spent fuel, electrolysis is used to recover fissile elements from nuclear waste samarium. The electrochemical behaviors of Sm(III) and Pb(II) were examined by CV, SWV, and OCP techniques in LiCl–KCl molten salts at 773 K. The redox mechanism of Sm(III) ions on the liquid Pb thin film electrode was analyzed. The results demonstrate that Sm(III) electro-reduction at the inert W electrode only occurred in a soluble–soluble electrochemical transition Sm(III)/Sm(II). Additionally, the kinetic parameters of samarium and lead ions were computed. The activation energies of diffusion for Sm(III) and Pb(II) were 32.92 kJ mol −1 and 35.21 kJ mol −1 , respectively. SmPb 3 and Sm 2 Pb intermetallic compounds were derived using constant potential electrolysis and constant current electrolysis at the Pb electrode in a molten salt system. The cathodic deposition output was characterized by XRD and SEM–EDS. The ICP-AES results showed that the average extraction ratio of Sm on the Pb electrode was about 94.23%.

研究领域: 核化学 · 电化学 · 材料科学
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