Determination of adsorbed species of hypophosphite electrooxidation on Ni electrode by in situ infrared with shell-isolated nanoparticle-enhanced Raman spectroscopy

被引:6
|
作者
Jiang, Yi-Feng [1 ]
Jiang, Bei [2 ]
Yang, Li-Kun [1 ]
Zhang, Meng [1 ]
Zhao, Liu-Bin [1 ]
Yang, Fang-Zu [1 ]
Cai, Wen-Bin [2 ]
Wu, De-Yin [1 ]
Zhou, Zhi-You [1 ]
Tian, Zhong-Qun [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
关键词
Hypophosphite; Electrooxidation; Surface-enhanced infrared absorption spectroscopy; Shell-isolated nanoparticle-enhanced; Raman spectroscopy; Adsorption orientation; ORGANOPHOSPHORUS COMPOUNDS; ABSORPTION FREQUENCIES; VIBRATIONAL-SPECTRA; NICKEL; DEPOSITION; OXIDATION;
D O I
10.1016/j.elecom.2014.08.002
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrooxidation of hypophosphite (H2PO2-) on Ni electrode was investigated at the molecular level by external-reflection Fourier-transform infrared spectroscopy (FTIR), surface-enhanced infrared absorption spectroscopy with attenuated total reflection (ATR-SEIRAS), and shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). The results of external-reflection FTIR demonstrated that H2PO2- could be oxidized to HPO32- at significantly low potentials (E < -1.0 V vs. SCE). ATR-SEIRAS result showed that H2PO2ad- could be adsorbed onto the Ni surface via O atoms. The adsorption orientation was further examined using SHINERS, and Ni-O stretching bands of metal-adsorbate vibration were directly detected. Comparative results of SHINERS and those obtained from the density functional theoretical calculation confirmed the adsorption orientation of H2PO2-. The present investigation verified for the first time the adsorption mechanism of H2PO2- electrooxidation on Ni surface through in situ spectroscopic data. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:5 / 9
页数:5
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