Kang Hungu, Cho Soo Jin, Kong Gyu Don, Yoon Hyo Jae
Department of Chemistry, Korea University, Seoul, 02841, Korea.
Nano Lett. 2022 Jun 22;22(12):4956-4962. doi: 10.1021/acs.nanolett.2c01669. Epub 2022 Jun 6.
This paper describes Li-ion intercalation into a pyrenyl-terminated self-assembled monolayer (SAM) on gold, inspired by the graphite anode in a Li-ion battery, and its effect on tunneling performance in a molecular junction incorporating the SAM. As the concentration of the Li-ion precursor ([LiPF]) increased from 0 to 10 M, the rectification ratio increased to ∼10. Further experiments revealed that the intercalation-induced changes in the orientation of PYR group and in the HOMO energy level account for the enhanced rectification. Treatment with high concentrations of LiPF (from 10 to 10 M) yielded a considerable solid electrolyte interphase (SEI), mainly composed of LiF, on the surface of the SAM, resulting in the disappearance of rectification. This was attributed to renormalization of the HOMO level back to that of the intact SAM, caused by the SEI layer. Our work demonstrates the interplay among Li-ion intercalation, SEI, and tunneling in the molecular junction, benefiting the research of molecular electronics as well as SAM-based batteries.
本文描述了受锂离子电池中石墨负极的启发,锂离子嵌入金表面芘基封端的自组装单分子层(SAM)的过程,以及其对包含该SAM的分子结中隧穿性能的影响。随着锂离子前体([LiPF])的浓度从0增加到10 M,整流比增加到约10。进一步的实验表明,嵌入诱导的芘基(PYR)基团取向和最高占据分子轨道(HOMO)能级的变化导致了整流增强。用高浓度的LiPF(从10到10 M)处理后,在SAM表面产生了主要由LiF组成的大量固体电解质界面(SEI),导致整流消失。这归因于SEI层导致HOMO能级恢复到完整SAM的能级。我们的工作展示了分子结中锂离子嵌入、SEI和隧穿之间的相互作用,对分子电子学以及基于SAM的电池的研究有益。