In situ X-ray absorption near edge structure studies and charge transfer kinetics of Na6[V10O28] electrodes. Issue 4 (16th January 2017)

• Record Type: Journal Article
• Authors: Chen, Han-Yi; Friedl, Jochen; Pan, Chun-Jern; Haider, Ali; Al-Oweini, Rami; Cheah, Yan Ling; Lin, Ming-Hsien; Kortz, Ulrich; Hwang, Bing-Joe; Srinivasan, Madhavi; Stimming, Ulrich
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 4(2017)
• Page Start: 3358
• Page End: 3365
• Publication Date: 2017-01-16
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp05768c
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : The electron transfer of Na6 [V10 O28 ] was investigated by in situ V K-edge X-ray absorption spectroscopy and chronoamperometric experiments for the first time. Abstract : Polyoxometalates (POMs) have been reported as promising electrode materials for energy storage applications due to their ability to undergo fast redox reactions with multiple transferred electrons per polyanion. Here we employ a polyoxovanadate salt, Na6 [V10 O28 ], as an electrode material in a lithium-ion containing electrolyte and investigate the electron transfer properties of Na6 [V10 O28 ] on long and short timescales. Looking at equilibrated systems, in situ V K-edge X-ray absorption near edge structure (XANES) studies show that all 10 V 5+ ions in Na6 [V10 O28 ] can be reversibly reduced to V 4+ in a potential range of 4–1.75 V vs. Li/Li + . Focusing on the dynamic response of the electrode to potential pulses, the kinetics of Na6 [V10 O28 ] electrodes and the dependence of the fundamental electron transfer rate k 0 on temperature are investigated. From these measurements we calculate the reorganization energy and compare it with theoretical predictions. The experimentally determined reorganization energy of λ = 184 meV is in line with the theoretical estimate and confirms the hypothesis of small values of λ for POMs due to electrostatic shielding of the redox center from the solvent.