TY - JOUR
T1 - Ultrasonication-assisted ultrafast preparation of multiwalled carbon nanotubes/Au/Co3O4 tubular hybrids as superior anode materials for oxygen evolution reaction
AU - Fang, Yiyun
AU - Li, Xinzhe
AU - Hu, Yiping
AU - Li, Feng
AU - Lin, Xiaoqing
AU - Tian, Min
AU - An, Xingcai
AU - Fu, Yan
AU - Jin, Jun
AU - Ma, Jiantai
N1 - Publisher Copyright:
© 2015 Elsevier B.V. All rights reserved.
PY - 2015/12/30
Y1 - 2015/12/30
N2 - Efficient and simple operation electrocatalysts for the oxygen evolution reaction (OER) are essential components of renewable energy technologies. Here, a novel, simple, and efficient routine is presented for the first time by constructing a high-efficiency anode catalyst for OER. With the aid of high intensity ultrasound, a uniformly loading, conductive multiwalled carbon nanotubes/metal/transition metal-oxide (CNTs-Au@Co3O4) tubular hybrids is synthesized. In alkaline media, the materials catalyze OER with an onset potential of 1.56 V vs. reversible hydrogen electrode (RHE) and overpotential only of 350 mV to achieve a stable current density of 10 mA cm-2 for at least 25 h. The unusual catalytic activity and stability is due to the following elements. Firstly, the tubular architecture not only provides sufficient active centers for OER, but also improves rapid mass/charge transport. Secondly, Co3O4 layer protects Au nanoparticles (NPs) against detachment. In addition, we also prove that the highest electronegativity metal Au accelerate the formation of catalytic active sites of CoIV species for OER. It is believed that this simple preparation method paves a way to fabricate a range of CNTs/metal/metal-oxide based composites as superior OER catalysts.
AB - Efficient and simple operation electrocatalysts for the oxygen evolution reaction (OER) are essential components of renewable energy technologies. Here, a novel, simple, and efficient routine is presented for the first time by constructing a high-efficiency anode catalyst for OER. With the aid of high intensity ultrasound, a uniformly loading, conductive multiwalled carbon nanotubes/metal/transition metal-oxide (CNTs-Au@Co3O4) tubular hybrids is synthesized. In alkaline media, the materials catalyze OER with an onset potential of 1.56 V vs. reversible hydrogen electrode (RHE) and overpotential only of 350 mV to achieve a stable current density of 10 mA cm-2 for at least 25 h. The unusual catalytic activity and stability is due to the following elements. Firstly, the tubular architecture not only provides sufficient active centers for OER, but also improves rapid mass/charge transport. Secondly, Co3O4 layer protects Au nanoparticles (NPs) against detachment. In addition, we also prove that the highest electronegativity metal Au accelerate the formation of catalytic active sites of CoIV species for OER. It is believed that this simple preparation method paves a way to fabricate a range of CNTs/metal/metal-oxide based composites as superior OER catalysts.
KW - Au nanoparticles
KW - CoO layer
KW - Multiwalled carbon nanotubes
KW - Oxygen evolution reaction
KW - Ultrasonic approach
UR - https://www.scopus.com/pages/publications/84942673530
U2 - 10.1016/j.jpowsour.2015.09.049
DO - 10.1016/j.jpowsour.2015.09.049
M3 - 文章
AN - SCOPUS:84942673530
SN - 0378-7753
VL - 300
SP - 285
EP - 293
JO - Journal of Power Sources
JF - Journal of Power Sources
ER -