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O+H(D)_(2)^(+)(v=0,1^(2)j=0)在两个不同势能面上的络合物动力学
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作者 王尉昱 卫来 《广东化工》 CAS 2022年第8期24-28,共5页
本文在基态势能面1^(2)A’’和第一激发态势能面1^(2)A’上研究了氧原子和氢分子离子的碰撞。这两个势能面的最小反应路径上均存在深势阱。本文计算了依赖碰撞能的中间络合物的平均寿命。结果显示在这两个势能面上,中间络合物的平均寿... 本文在基态势能面1^(2)A’’和第一激发态势能面1^(2)A’上研究了氧原子和氢分子离子的碰撞。这两个势能面的最小反应路径上均存在深势阱。本文计算了依赖碰撞能的中间络合物的平均寿命。结果显示在这两个势能面上,中间络合物的平均寿命随着碰撞能的增加而减小。反应存在两种机制,一个是直接反应,另外一个是间接反应。在研究的碰撞能范围内,间接反应占据了主导地位。然而,随着碰撞能的升高,直接反应机制变得越来越重要。另外,本工作还详细研究了反应物激发态和同位素效应对标量性质的影响。尽管反应物振动激发对中间络合物的平均寿命影响很小,但它显著地提高了基态势能面上直接反应的轨线数。相反,在激发态势能面上,反应物振动激发减少了间接反应的轨线数并减小了中间络合物的平均寿命。同位素效应对标量性质没有影响。 展开更多
关键词 分子动力学 络合物寿命 势能面 反应截面 振转态分布
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High interfacial-energy heterostructure facilitates large-sized lithium nucleation and rapid Li+desolvation process
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作者 Zhipeng Wen Yuanhong Kang +5 位作者 Qilong Wu Xiu Shen Pengbin Lai Yang Yang Cheng Chao Li Jinbao Zhao 《Science Bulletin》 SCIE EI CAS CSCD 2022年第24期2531-2540,M0004,共11页
High interfacial energy Li^(0)-electrolyte interface contributes to larger Li^(0) nucleation embryos and a more stable interface,so the interfacial energy is essential for highly reversible Li^(0) deposition/stripping... High interfacial energy Li^(0)-electrolyte interface contributes to larger Li^(0) nucleation embryos and a more stable interface,so the interfacial energy is essential for highly reversible Li^(0) deposition/stripping.Herein,a high interfacial-energy artificial solid electrolyte interphase(SEI)with rich LiF embedded in lithiated poly-2-acrylamido-2-methylpropane sulfonic acid(PAMPS-Li)network is designed to realize favorable Li^(0) nucleation and rapid desolvation of Li+simultaneously.The Li-F bonds in LiF(001)exhibit stronger ion-dipole interactions with Li atoms,offering higher interfacial energies.When the growth surface energy and total interfacial energy of Li^(0) are balanced,the high interfacial energy SEI with abundant LiF can promote the formation of larger Li^(0) nucleation embryos.In addition,the PAMPS-Li with immobilized anions presents weaker interaction with Li^(0) and possesses higher polymer-Li interfacial energy,and its amide and sulfonic acid groups exhibit higher binding energies with Li^(+).Therefore,PAMPS-Li can easily promote the Li+to escape from the solvent sheath and weaken the desolvation energy barrier.The highly reversible Li^(0) deposition behavior with restricted side reactions is achieved based on the synergistic modification of high interfacial energy SEI with heterostructure.Most importantly,lifespan of multi-layered Li^(0) pouch cell(330 Wh kg-1)with a low N/P ratio(1.67)is over 100 cycles,verifying its potential practical application. 展开更多
关键词 Crystalline LiF-rich High interfacial energy Large metallic Li^(0) nucleate size Rapid Li^(+) desolvation Pouch cell
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