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<title>Solid Electrolyte Interphase (SEI) at TiO2 Electrodes in Li-Ion Batteries: Defining Apparent and Effective SEI Based on Evidence from X-ray Photoemission Spectroscopy and Scanning Electrochemical Microscopy</title>
<creator>Ventosa Arbaizar, Edgar</creator>
<creator>Madej, Edyta</creator>
<creator>Zampardi, Giorgia</creator>
<creator>Mei, Bastian</creator>
<creator>Weide, Philipp</creator>
<creator>Antoni, Hendrik</creator>
<creator>La Mantia, Fabio</creator>
<creator>Muhler, Martin</creator>
<creator>Schuhmann, Wolfgang</creator>
<subject>Li-on batteries</subject>
<subject>Solid electrolyte interphase</subject>
<subject>X-ray photoemission</subject>
<subject>Scanning electrochemical microscopy</subject>
<subject>Titanium dioxide</subject>
<description>The high (de)lithiation potential of TiO2 (ca. 1.7 V vs Li/Li+ in 1 M Li+) decreases the voltage and, thus, the energy density of a corresponding Li-ion battery. On the other hand, it offers several advantages such as the (de)lithiation potential far from lithium deposition or absence of a solid electrolyte interphase (SEI). The latter is currently under controversial debate as several studies reported the presence of a SEI when operating TiO2 electrodes at potentials above 1.0 V vs Li/Li+. We investigate the formation of a SEI at anatase TiO2 electrodes by means of X-ray photoemission spectroscopy (XPS) and scanning electrochemical microscopy (SECM). The investigations were performed in different potential ranges, namely, during storage (without external polarization), between 3.0–2.0 V and 3.0–1.0 V vs Li/Li+, respectively. No SEI is formed when a completely dried and residues-free TiO2 electrode is cycled between 3.0 and 2.0 V vs Li/Li+. A SEI is detected by XPS in the case of samples stored for 6 weeks or cycled between 3.0 and 1.0 V vs Li/Li+. With use of SECM, it is verified that this SEI does not possess the electrically insulating character as expected for a “classic” SEI. Therefore, we propose the term apparent SEI for TiO2 electrodes to differentiate it from the protecting and effective SEI formed at graphite electrodes.</description>
<date>2026-02-17</date>
<date>2026-02-17</date>
<date>2016-12</date>
<type>info:eu-repo/semantics/article</type>
<identifier>1944-8244</identifier>
<identifier>https://hdl.handle.net/10259/11377</identifier>
<identifier>10.1021/acsami.6b13306</identifier>
<identifier>1944-8252</identifier>
<language>eng</language>
<relation>ACS Applied Materials &amp; Interfaces. 2016, V. 9, n. 3, p. 3123-3130</relation>
<relation>https://doi.org/10.1021/acsami.6b13306</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<publisher>American Chemical Society</publisher>
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