P掺杂LiNH_(2)团簇与LiH反应机理的密度泛函理论研究及一种新储放氢机制  

Density functional theory on reaction mechanism between p-doped LiNH_(2) clusters and LiH and a new hydrogen storage and desorption mechanism

作　　者：董肖 Dong Xiao(Xinjiang Laboratory of Phase Transitions and Microstructures in Condensed Matters,College of Physical Science and Technology,Yili Normal University,Yining 835000,China)

机构地区：[1]伊犁师范大学物理科学与技术学院,新疆凝聚态相变与微结构实验室,伊宁835000

出　　处：《物理学报》2023年第15期36-44,共9页Acta Physica Sinica

基　　金：新疆维吾尔自治区高校科研计划(批准号:XJEDU2022P094,XJEDU2017S050)资助的课题.

摘　　要：采用密度泛函理论,对P掺杂的(LiNH_(2))_(n)(n=1-4)团簇与LiH的反应机理进行理论分析,反应中的驻点进行了构型优化,通过频率和内禀反应坐标的计算来判断各驻点及其相互连接关系的正确性.计算了能够反映反应物的稳定性参数.结果表明:P掺杂后对最低未占据轨道影响较小,最高占据轨道分布有较大幅度向掺杂原子处的转移,失电子区域集中在P原子处.经P原子掺杂,降低了氨基锂团簇的稳定性,反应脱氢能垒有所降低.反应更倾向于由-PH_(2)官能团脱氢和在—NH2官能团处储氢.在循环储放氢过程中,实现氢在—NH2和-PH_(2)官能团之间的有效转移,可进一步改善该材料的储放氢的可逆性.Hydrogen energy is considered a clean energy with great development prospects.In the field of hydrogen energy applications,the solid-state chemical hydrogen storage method using hydrogen storage materials as media has received widespread attention due to its safety and high hydrogen storage density.In the research on metal-N-H system hydrogen storage materials,current studies focus on improving the kinetic conditions for hydrogen storage.In this study,the B3LYP hybrid functional method of density functional theory is used to investigate the reaction mechanism between P-doped LiNH2 clusters and LiH at a cluster level,and explore the effects of doping,in addition a new hydrogen storage mechanism called“secondary hydrogen transfer”is proposed.The full-geometry optimization of(LiNH2)n(n=1–4)clusters and their P-doped clusters at the 6-31G(d,p)basis set level are carried out,and their corresponding most stable configurations are obtained.The distribution and stability of the frontier orbitals of the relevant reactants are calculated.Using the same method and basis set,the theoretical calculation and analysis of the reaction mechanism between P-doped(LiNH2)n(n=1–4)clusters and LiH are conducted,including the configuration optimization of the stationary points in each reaction path,and the correctness of the connection between the stationary points is determined through frequency and intrinsic reaction coordinate calculations.The results show that P doping has a small effect on the lowest unoccupied molecular orbital,while the highest occupied molecular orbital has a significant transition towards the doping atom,and the electron-deficient region is concentrated at the P atom.P doping reduces the stability of the lithium amide clusters and enhances their ability to participate in chemical reactions and reaction activity,and the reaction dehydrogenation energy barrier decreases.The reaction dehydrogenation energy barrier between P-doped LiNH2 clusters and LiH is significantly lower than that between LiNH2 and LiH

关 键 词：储氢材料 密度泛函理论 过渡态 

分 类 号：O641.1[理学—物理化学]