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Small Groups, Big Impact: Eliminating Li+ Traps in Single-Ion Conducting Polymer Electrolytes.

ABSTRACT: Single-ion conducting polymer electrolytes exhibit great potential for next-generation high-energy-density Li metal batteries, although the lack of sufficient molecular-scale insights into lithium transport mechanisms and reliable understanding of key correlations often limit the scope of modification and design of new materials. Moreover, the sensitivity to small variations of polymer chemical structures (e.g., selection of specific linkages or chemical groups) is often overlooked as potential design parameter. In this study, combined molecular dynamics simulations and experimental investigations reveal molecular-scale correlations among variations in polymer structures and Li+ transport capabilities. Based on polyamide-based single-ion conducting quasi-solid polymer electrolytes, it is demonstrated that small modifications of the polymer backbone significantly enhance the Li+ transport while governing the resulting membrane morphology. Based on the obtained insights, tailored materials with significantly improved ionic conductivity and excellent electrochemical performance are achieved and their applicability in LFP||Li and NMC||Li cells is successfully demonstrated.

SUBMITTER: Borzutzki K

PROVIDER: S-EPMC7452907 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Small Groups, Big Impact: Eliminating Li<sup>+</sup> Traps in Single-Ion Conducting Polymer Electrolytes.

Borzutzki Kristina K Dong Dengpan D Wölke Christian C Kruteva Margarita M Stellhorn Annika A Winter Martin M Bedrov Dmitry D Brunklaus Gunther G

iScience 20200729 8

Single-ion conducting polymer electrolytes exhibit great potential for next-generation high-energy-density Li metal batteries, although the lack of sufficient molecular-scale insights into lithium transport mechanisms and reliable understanding of key correlations often limit the scope of modification and design of new materials. Moreover, the sensitivity to small variations of polymer chemical structures (e.g., selection of specific linkages or chemical groups) is often overlooked as potential ...[more]

PMID: 32798969

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Project description:Electrospun nanocomposite polymer blend poly(vinylidene difluoride-co-hexafluoropropylene) (PVDF-HFP)/poly(methyl methacrylate) (PMMA) membranes with a novel dispersion of x wt % of one-dimensional (1D) TiO2 nanofiber fillers (x = 0.0-0.8 in steps of 0.2) were developed using the electrospinning technique. The developed nanocomposite polymer membranes were activated using various redox agents such as LiI, NaI, KI, and tetrabutyl ammonium iodide (TBAI). Introduction of the 1D TiO2 nanofiber fillers improves the amorphous nature of the blended polymer membrane, as confirmed through X-ray diffraction (XRD) and Fourier transform infrared (FTIR), and yielded an electrolyte uptake of over 480% for a 6 wt % TiO2 nanofiber filler-dispersed sample. PVDF-HFP/PMMA-1D 6 wt % TiO2 nanofiber fillers with the LiI-based redox electrolyte provided a high conductivity of 2.80 × 10-2 S cm-1 and a power conversion efficiency (PCE) of 8.08% to their fabricated dye-sensitized solar cells (DSSCs). The observed better ionic conductivity and efficiency of the fabricated DSSCs could be due to the faster movement of the smaller-ionic-radius (Li) ions entrapped inside the amorphous polymer. This enhanced mobility of ions in the quasi-solid electrolyte leads to faster regeneration of the depleting electrons in the photoanode, resulting in improved efficiency. Further, the achieved high conductivity was analyzed in terms of the dynamics and relaxation mechanisms involved by the ionic charge carriers with complex impedance spectroscopy using a random barrier model and Havriliak-Negami formulation. It was observed that the high-conducting PVDF-HFP/PMMA-1D 6 wt % TiO2 nanofiber fillers with LiI-based redox electrolyte show better ac conductivity parameters such as a σ of 5.82 × 10-2 S cm-1, ωe (12685 rad s-1), τe (0.909 × 10-4 s), and n (0.578). Also, dielectric studies revealed that the high-conducting sample has a higher dielectric constant and subsequently high loss. The J-V characteristics were studied using the equivalent circuit of a single-diode model, and the parameters influencing the photovoltaic performance were determined by Symbiotic Organisms Search (SOS) algorithm. The results suggest that the high-efficient sample possesses a minimum series resistance of 1.33 Ω and a maximum shunt resistance of 997 Ω. Hence, the highest-conducting electrospun-blended polymeric nanocomposite (PVDF-HFP-PMMA-6 wt % TiO2 nanofiber fillers) with LiI-based redox agent and tert-butyl pyridine (TBP) additive as the polymer quasi-solid electrolyte nanofibrous membrane can be a better electrolyte for high-performance dye-sensitized solar cell applications.

Dataset Information

Small Groups, Big Impact: Eliminating Li+ Traps in Single-Ion Conducting Polymer Electrolytes.

Publications

Small Groups, Big Impact: Eliminating Li<sup>+</sup> Traps in Single-Ion Conducting Polymer Electrolytes.

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