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000605489 1001_ $$0P:(DE-H253)PIP1015737$$aBrinker, Manuel$$b0
000605489 245__ $$aA Mott-Schottky analysis of mesoporous silicon in aqueous electrolyte solution by electrochemical impedance spectroscopy
000605489 260__ $$aNew York, NY [u.a.]$$bElsevier$$c2024
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000605489 520__ $$aNanoporosity in silicon leads to completely new functionalities of this mainstream semiconductor.In recent years, it has been shown that filling the pores with aqueous electrolytes in addition opensa particularly wide field for modifying and achieving active control of these functionalities, e.g.,for electrochemo-mechanical actuation and tunable photonics, or for the design of on-chip superca-pacitors. However, a mechanistic understanding of these new features has been hampered by thelack of a detailed characterization of the electrochemical behavior of mesoporous silicon in aqueouselectrolytes. Here, the capacitive, potential-controlled charging of the electrical double layer in amesoporous silicon electrode (pore diameter 7 nm) imbibed with perchloric acid solution is studiedby electrochemical impedance spectroscopy. Thorough measurements with detailed explanationsof the observed phenomena lead to a comprehensive understanding of the capacitive properties ofporous silicon. An analysis based on the Mott-Schottky equation allows general conclusions to bedrawn about the state of the band structure within the pore walls. Essential parameters such as theflat band potential, the doping density and the width of the space charge region can be determined.A comparison with bulk silicon shows that the flat band potential in particular is significantly al-tered by the introduction of nanopores, as it shifts from 1.4 ± 0.1 V to 1.9 ± 0.2 V. Overall, thisstudy provides a unique insight into the electrochemical processes, especially the electrical doublelayer charging, of nanoporous semiconductor electrodes.
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000605489 7870_ $$0PUBDB-2024-01068$$aBrinker, Manuel et.al.$$d2024$$iIsParent$$rarXiv:2312.04252$$tA Mott-Schottky Analysis of Mesoporous Silicon in Aqueous Electrolyte by Electrochemical Impedance Spectroscopy
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