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Highly mobile and reactive state of hydrogen in metal oxide semiconductors at room temperature.


ABSTRACT: Hydrogen in metal oxides usually strongly associates with a neighboring oxygen ion through an O-H bond and thus displays a high stability. Here we report a novel state of hydrogen with unusually high mobility and reactivity in metal oxides at room temperature. We show that freshly doped hydrogen in Nb₂O₅ and WO₃ polycrystals via electrochemical hydrogenation can reduce Cu²⁺ ions into Cu⁰ if the polycrystals are immersed in a CuSO₄ solution, while this would not happen if the hydrogenated polycrystals have been placed in air for several hours before the immersion. Time-dependent studies of electrochemically hydrogenated rutile single crystals reveal two distinct states of hydrogen: one as protons covalently bonded to oxygen ions, while the other one is highly unstable with a lifetime of just a few hours. Observation of this mobile and reactive state of hydrogen will provide new insight into numerous moderate and low temperature interactions between metal oxides and hydrogen.

SUBMITTER: Chen WP 

PROVIDER: S-EPMC3818659 | biostudies-literature | 2013 Nov

REPOSITORIES: biostudies-literature

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Highly mobile and reactive state of hydrogen in metal oxide semiconductors at room temperature.

Chen Wan Ping WP   He Ke Feng KF   Wang Yu Y   Chan Helen Lai Wah HL   Yan Zijie Z  

Scientific reports 20131106


Hydrogen in metal oxides usually strongly associates with a neighboring oxygen ion through an O-H bond and thus displays a high stability. Here we report a novel state of hydrogen with unusually high mobility and reactivity in metal oxides at room temperature. We show that freshly doped hydrogen in Nb₂O₅ and WO₃ polycrystals via electrochemical hydrogenation can reduce Cu²⁺ ions into Cu⁰ if the polycrystals are immersed in a CuSO₄ solution, while this would not happen if the hydrogenated polycry  ...[more]

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