Liu Zhihao, Lunchev Andrey V, Li Wen, Ruan Shuangchen, Yazami Rachid, Grimsdale Andrew C, Su Haibin
School of Material Science & Engineering, Nanyang Technological University, 639798, Singapore.
Energy Research Institute, Tianneng Group, Huaxi Industrial Function Zone, Changxing County, Zhejiang 313100, China.
ACS Omega. 2019 Mar 4;4(3):4707-4711. doi: 10.1021/acsomega.8b03621. eCollection 2019 Mar 31.
The conductivity and open-circuit voltage (OCV) of lithium-solvated electron solutions (LiSESs) based on anthracene in tetrahydrofuran were studied by both experimental measurements and density functional theory calculations with a range-separated functional based on the M06 form and the Solvation Model based on Density (SMD). The OCV was found to decrease with increasing temperature and the ratio of lithium to anthracene. The enthalpy change (Δ) of LiSESs was the internal energy change of the cell reaction. The conductivity of LiSESs exhibited a weakly metallic-like behavior. The electron transport was facilitated by molecular collisions promoted by the formation of dimeric structures as intermediates. The conductivity of LiSESs at 295.15 K presents positive correlation with the entropy change (Δ) associated with the variation in the ratio of lithium to poly-aromatic hydrocarbon, including -terphenyl, anthracene, and triphenylene.
通过实验测量以及基于M06形式的范围分离泛函和基于密度的溶剂化模型(SMD)的密度泛函理论计算,研究了基于蒽在四氢呋喃中的锂溶剂化电子溶液(LiSESs)的电导率和开路电压(OCV)。发现OCV随温度以及锂与蒽的比例增加而降低。LiSESs的焓变(Δ)是电池反应的内能变化。LiSESs的电导率表现出类似弱金属的行为。电子传输通过形成二聚体结构作为中间体促进的分子碰撞而得以实现。LiSESs在295.15 K时的电导率与锂与多环芳烃(包括对三联苯、蒽和三亚苯)比例变化相关的熵变(Δ)呈正相关。