氧化还原
电化学
电子转移
粘土矿物
表征(材料科学)
化学
无机化学
材料科学
地质学
电极
化学工程
矿物学
纳米技术
物理化学
工程类
作者
Christopher A. Gorski,Laura Klüpfel,Andreas Voegelin,Michael Sander,Thomas B. Hofstetter
摘要
Structural Fe in clay minerals is an important, albeit poorly characterized, redox-active phase found in many natural and engineered environments. This work develops an experimental approach to directly assess the redox properties of a natural Fe-bearing smectite (ferruginous smectite, SWa-1, 12.6 wt % Fe) with mediated electrochemical reduction (MER) and oxidation (MEO). By utilizing a suite of one-electron-transfer mediating compounds to facilitate electron transfer between structural Fe in SWa-1 and a working electrode, we show that the Fe2+/Fe3+ couple in SWa-1 is redox-active over a large range of potentials (from EH = −0.63 V to +0.61 V vs SHE). Electrochemical and spectroscopic analyses of SWa-1 samples that were subject to reduction and re-oxidation cycling revealed both reversible and irreversible structural Fe rearrangements that altered the observed apparent standard reduction potential (EH⌀) of structural Fe. EH⌀-values vary by as much as 0.56 V between SWa-1 samples with different redox histories. The wide range of EH-values over which SWa-1 is redox-active and redox history-dependent EH⌀-values underscore the importance of Fe-bearing clay minerals as redox-active phases in a wide range of redox regimes.
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