Fluorine doped CNTs for efficient OER activity outperforming iridium supported carbon electrocatalyst

被引:19
作者
Ali, Zulfiqar [1 ]
Mehmood, Mazhar [1 ]
Ahmad, Jamil [1 ]
Fatima, Aiman [2 ]
Ali, Muhammad [3 ]
机构
[1] Pakistan Inst Engn & Appl Sci PIEAS, Dept Met & Mat Engn, Natl Ctr Nanotechnol, Islamabad 45650, Pakistan
[2] Pakistan Inst Engn & Appl Sci PIEAS, Dept Chem Engn, Islamabad 45650, Pakistan
[3] Univ Sci & Technol China USTC, Sch Mat Sci & Engn, Hefei 230026, Peoples R China
关键词
F-doped CNTs; Solid state fusion; XPS; Electrocatalysis; OER; OXYGEN EVOLUTION REACTION; NANOSHEETS; NANOTUBES;
D O I
10.1007/s10800-021-01600-x
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Herein, we report the low-temperature fluorine doping into carbon nanotubes (CNTs) by solid-state fusion method using xenon fluoride (XeF2) as a precursor of fluorine. The XPS analysis revealed that fluorine atoms were covalently attached to CNTs and about 5.1 at.% fluorine was successfully doped into CNTs. The transmission electron microscope images showed that the outer surface of thinner CNTs becomes rough after fluorine incorporation with a similar tube diameter as that of undoped CNTs. The electrochemical testing for oxygen evolution reaction (OER) in alkaline media shows that the F-doped CNTs are better OER electrocatalysts than their undoped counterpart and noble metal iridium supported carbon electrocatalyst i.e. Ir/C (20 wt% Ir) under identical conditions. The F-doped CNTs exhibited 25 mV and 60 mV lower OER overpotentials than noble metal iridium supported electrocatalyst and undoped CNTs respectively. The better OER performance of F-doped CNTs is attributed to the surface modification of inert sp(2) hybridized carbon layers by more electronegative fluorine atoms which create semi ionic C-F and covalent C-F active sites for efficient OER activity.
引用
收藏
页码:1573 / 1581
页数:9
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