物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2012年
4期
818-821
,共4页
李田田%王朝阳%邢丽丹%李伟善%彭彬%许梦清%顾凤龙%胡社军
李田田%王朝暘%邢麗丹%李偉善%彭彬%許夢清%顧鳳龍%鬍社軍
리전전%왕조양%형려단%리위선%팽빈%허몽청%고봉룡%호사군
锂离子电池%过充电保护添加剂%1,4-二甲氧基苯%反应机理%密度泛函理论
鋰離子電池%過充電保護添加劑%1,4-二甲氧基苯%反應機理%密度汎函理論
리리자전지%과충전보호첨가제%1,4-이갑양기분%반응궤리%밀도범함이론
Lithium ion battery%Overcharge protection additive%1,4-Dimethoxy benzene%Reaction mechanism%Density functional theory
采用密度泛函理论(B3LYP/6-311+G(d,p))和MP216-311+G(d,p)方法,研究锂离子电池过充电保护添加剂1,4-二甲氧基苯(p-DMOB)的作用机理.计算结果表明,在过充时,p-DMOB优先于溶剂分子(乙基甲基碳酸酯、二甲基碳酸酯、碳酸乙酯)发生氧化反应.用B3LYP和MP2计算所得的p-DMOB理论氧化电位接近,分别为4.12和4.05V (vs Li/Li+).p-DMOB氧化时首先失去一个电子,生成p-DMOB+*正离子自由基,用B3LYP和MP2方法计算所得的相应能量变化分别为701.24和728.27 kJ· mol-1.失去电子后苯环的共轭性受到破坏,随后p-DMOB”苯环上的CH键发生断裂,失去H+并形成p-DMOB·自由基,用B3LYP和MP2方法计算所得的相应能量变化分别为1349.78和1810.99 kJ· mol-1,p-D MOB·自由基很小稳定,会在电极表面发生聚合反应形成聚合物膜,用B3LYP和MP2方法计算所得的相应能量变化分别为-553.37和-1331.20kJ·mol-1.
採用密度汎函理論(B3LYP/6-311+G(d,p))和MP216-311+G(d,p)方法,研究鋰離子電池過充電保護添加劑1,4-二甲氧基苯(p-DMOB)的作用機理.計算結果錶明,在過充時,p-DMOB優先于溶劑分子(乙基甲基碳痠酯、二甲基碳痠酯、碳痠乙酯)髮生氧化反應.用B3LYP和MP2計算所得的p-DMOB理論氧化電位接近,分彆為4.12和4.05V (vs Li/Li+).p-DMOB氧化時首先失去一箇電子,生成p-DMOB+*正離子自由基,用B3LYP和MP2方法計算所得的相應能量變化分彆為701.24和728.27 kJ· mol-1.失去電子後苯環的共軛性受到破壞,隨後p-DMOB”苯環上的CH鍵髮生斷裂,失去H+併形成p-DMOB·自由基,用B3LYP和MP2方法計算所得的相應能量變化分彆為1349.78和1810.99 kJ· mol-1,p-D MOB·自由基很小穩定,會在電極錶麵髮生聚閤反應形成聚閤物膜,用B3LYP和MP2方法計算所得的相應能量變化分彆為-553.37和-1331.20kJ·mol-1.
채용밀도범함이론(B3LYP/6-311+G(d,p))화MP216-311+G(d,p)방법,연구리리자전지과충전보호첨가제1,4-이갑양기분(p-DMOB)적작용궤리.계산결과표명,재과충시,p-DMOB우선우용제분자(을기갑기탄산지、이갑기탄산지、탄산을지)발생양화반응.용B3LYP화MP2계산소득적p-DMOB이론양화전위접근,분별위4.12화4.05V (vs Li/Li+).p-DMOB양화시수선실거일개전자,생성p-DMOB+*정리자자유기,용B3LYP화MP2방법계산소득적상응능량변화분별위701.24화728.27 kJ· mol-1.실거전자후분배적공액성수도파배,수후p-DMOB”분배상적CH건발생단렬,실거H+병형성p-DMOB·자유기,용B3LYP화MP2방법계산소득적상응능량변화분별위1349.78화1810.99 kJ· mol-1,p-D MOB·자유기흔소은정,회재전겁표면발생취합반응형성취합물막,용B3LYP화MP2방법계산소득적상응능량변화분별위-553.37화-1331.20kJ·mol-1.
The reaction mechanism of 1,4-dimethoxybenzene (p-DMOB) as an overcharge protection additive for lithium ion batteries was determined by theoretical calculation of density functional theory (DFT) at the level of B3LYP/6-311 +G(d,p) and MP2/6-311 +G(d,p).It was found that p-DMOB is oxidized prior to the solvents,ethyl methyl carbonate,dimethyl carbonate,and ethylene carbonate,when the lithium ion battery is overcharged.The calculated oxidative potentials of p-DMOB by B3LYP and MP2 methods are well in agreement at 4.12 and 4.05 V (vs Li/Li+),respectively.The initial oxidation of p-DMOB involves a one-electron transfer resulting in a radical cation p-DMOB+*.The corresponding energy variations were 701.24 and 728.27 kJ.mol-1 from B3LYP and MP2 calculations,respectively.The p-DMOB+* species then loses one proton forming a radical p-DMOB- through the breaking of a C-- H bond on the benzene ring,with the corresponding energy variations of 1349.78 and 1810.99 kJ·mol-1 for B3LYP and MP2,respectively.The p-DMOB·species is unstable and copolymerizes forming an insulated polymer with the corresponding energy variations of -553.37 and -1331.20 kJ.mol-~ for B3LYP and MP2,respectively.