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Safety Risks and Countermeasures of Lithium-ion Battery Energy Storage Power Station
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作者 Lifei Lian hanbin hu 《Journal of Electronic Research and Application》 2025年第3期254-261,共8页
With the continuous emergence of new energy storage technology innovation in the field of electrochemical energy storage in China,different megawatt-grade lithium-ion battery energy storage projects have been implemen... With the continuous emergence of new energy storage technology innovation in the field of electrochemical energy storage in China,different megawatt-grade lithium-ion battery energy storage projects have been implemented,promoting the high-quality development of the energy storage industry.In the context of vigorously promoting the energy consumption revolution and enhancing the green transformation and development momentum,strengthening the safety construction of lithium-ion battery energy storage is of great importance to realize the transformation of energy structure and improve the utilization efficiency of renewable energy.However,in recent years,frequent safety accidents of lithium-ion battery energy storage power stations,such as fires,have aroused the public’s high attention to the construction of lithium-ion battery energy storage power stations,affecting the large-scale development of energy storage power stations.Based on this,this paper analyzes the safety risks of lithium-ion battery energy storage power stations and focuses on how to improve their safety performance. 展开更多
关键词 Lithium-ion battery energy storage power station Safety risk Apply policy
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多酸基多孔离子晶体的前沿与应用 被引量:1
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作者 田文玉 郭琳 +3 位作者 胡汉斌 楚进锋 何蕾 宋宇飞 《科学通报》 EI CAS CSCD 北大核心 2022年第7期655-669,共15页
多酸基多孔离子晶体(polyoxometalates-based porous ionic crystals,PPICs)是由带相反电荷的无机多酸阴离子(polyoxometalates,POMs)和配位化合物阳离子簇通过离子键或氢键相互作用形成的一类独特的多孔材料.其孔道尺寸可调、组成可控... 多酸基多孔离子晶体(polyoxometalates-based porous ionic crystals,PPICs)是由带相反电荷的无机多酸阴离子(polyoxometalates,POMs)和配位化合物阳离子簇通过离子键或氢键相互作用形成的一类独特的多孔材料.其孔道尺寸可调、组成可控、合成方法简便.PPICs兼具阴、阳离子的优点,各组分间协同驱动,表现出比单一组分更优异的性能.通过对PPICs各组分的合理设计,可以有效调控其理化性质.本文系统地总结了PPICs的结构组成,阐述了PPICs可调的孔道结构、独特的氧化还原特征、强酸性及磁性等性质,列举了PPICs在选择性吸附、酸催化、电化学等领域的应用进展,并对其未来发展方向进行了展望. 展开更多
关键词 多酸 离子晶体 多孔性 氧化还原性 选择性吸附
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Covalently tethering disulfonic acid moieties onto polyoxometalate boosts acid strength and catalytic performance for hydroxyalkylation/alkylation reaction 被引量:1
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作者 Lifei Lian Yubing Liu +6 位作者 Xianfeng Yi hanbin hu Xiang Chen Hongqiang Li Wei Chen Anming Zheng Yu-Fei Song 《Science China Chemistry》 SCIE EI CSCD 2022年第4期699-709,共11页
Solid acid catalysts are widely used in the production of various high-value added and industrially important chemicals.Although the use of organosilicon compounds to modify the vacancy site has been extensively studi... Solid acid catalysts are widely used in the production of various high-value added and industrially important chemicals.Although the use of organosilicon compounds to modify the vacancy site has been extensively studied,the covalent tethering-SO_(3)H functionalized organosilicon modified polyoxometalates(POMs)has been rarely reported.In this work,two catalysts(TBA_(4)[SiW_(11)O_(39)(O(SiC_(3)H_(6)SO_(3)H)_(2))](compound 2)and TBA_(4)[SiW_(11)O_(39)(O(SiC_(8)H_(8)SO_(3)H)_(2))](compound 3))were synthesized successfully through covalently grafting different sulfonic acid(-SO_(3)H)groups onto[SiW_(11)O_(39)]^(8−)cluster,respectively.Compound 2 was achieved by surface grafting and in situ oxidation(3-mercaptopropyl)-trimethoxysilane,while compound 3 was achieved by surface grafting of 2-(4-chlorosulfonylphenyl)ethyltrimethoxysilane.Strong Brønsted acid strength of compounds 2 and 3 can be demonstrated by different methods including potentiometric titration,pyridine adsorption studies,and the ^(31)P trimethylphosphine oxides(TMPO)nuclear magnetic resonance(NMR).The systematic investigation of the relationship among POM structures,acid strength,and electron density was carried out based on density functional theory(DFT)calculation and experimental results,which revealed that covalent modification of compounds 2 and 3 decreased the electron density of the O-H bond,and promoted the release of H^(+).When applied in hydroxyalkylation/alkylation(HAA)reaction of 2-methylfuran(2-MF)with cyclohexanone,compound 2 exhibited better catalytic performance with conversion of ~93%,monocyclic fuel precursors(1a)yield of 79.9% and selectivity of 85.7% than compound 3,which can be attributed to strong Brønsted acid and the intramolecular hydrogen-bonding interactions between the neighboring -SO_(3)H moieties in compound 2.Finally,compound 2 also showed excellent catalytic activity in the HAA reaction of 2-MF with several different aldehydes and ketones(e.g.,furfuraldehyde,5-methylfurfuraldehyde,acetone,butyraldehyde and 4-methoxybenzaldehyde).This result opens a new pathway for design and fabrication of novel solid acid catalysts. 展开更多
关键词 POLYOXOMETALATES sulfonic acid covalent modifications acid catalysis alkylation reaction
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