TY - JOUR
T1 - Enhanced electrocatalytic activity of platinum supported on nitrogen modified ordered mesoporous carbon
AU - Guo, Yunxia
AU - He, Jianping
AU - Wang, Tao
AU - Xue, Hairong
AU - Hu, Yuanyuan
AU - Li, Guoxian
AU - Tang, Jing
AU - Sun, Xing
PY - 2011/11/15
Y1 - 2011/11/15
N2 - Nitrogen-modified ordered mesoporous carbon is synthesized via the 900 °C carbonization of polyaniline-coated mesoporous carbon. The electronic states of nitrogen atoms are investigated by XPS technique. Pyridinic nitrogen and quaternary nitrogen generate disorders and curvatures on the surface of graphitic carbon layers with nitrogen atoms replacing carbon atoms at the edges and the interior of carbon stacking, and thus offering beneficial anchoring sites for PtCl62- ions. Pyridinic nitrogen and pyrrolic nitrogen offer p electrons to the sp2 hybridized graphitic carbon layers, decreasing the inner electrical resistance of the catalytic carbon layer, enhancing the rate of proton diffusion, and transporting more free electrons to oxidative platinum. Due to the advantageous modification of the electronic structure of carbon atoms, platinum nanoparticles with a narrow size distribution are homogenously dispersed onto the surface of nitrogen-modified ordered mesoporous carbon, as evidenced by TEM images. Electrochemical tests show that the samples loaded platinum calcined at the 900 °C exhibit the optimum loading performance among as-made catalysts and a gradually decreased decay in electro-catalytic activity with time, with the current density stabilized at 3.64 mA cm-2, which is far higher than that of mesoporous carbon (0.15 mA cm-2).
AB - Nitrogen-modified ordered mesoporous carbon is synthesized via the 900 °C carbonization of polyaniline-coated mesoporous carbon. The electronic states of nitrogen atoms are investigated by XPS technique. Pyridinic nitrogen and quaternary nitrogen generate disorders and curvatures on the surface of graphitic carbon layers with nitrogen atoms replacing carbon atoms at the edges and the interior of carbon stacking, and thus offering beneficial anchoring sites for PtCl62- ions. Pyridinic nitrogen and pyrrolic nitrogen offer p electrons to the sp2 hybridized graphitic carbon layers, decreasing the inner electrical resistance of the catalytic carbon layer, enhancing the rate of proton diffusion, and transporting more free electrons to oxidative platinum. Due to the advantageous modification of the electronic structure of carbon atoms, platinum nanoparticles with a narrow size distribution are homogenously dispersed onto the surface of nitrogen-modified ordered mesoporous carbon, as evidenced by TEM images. Electrochemical tests show that the samples loaded platinum calcined at the 900 °C exhibit the optimum loading performance among as-made catalysts and a gradually decreased decay in electro-catalytic activity with time, with the current density stabilized at 3.64 mA cm-2, which is far higher than that of mesoporous carbon (0.15 mA cm-2).
KW - Electrocatalytic activity
KW - Fuel cell
KW - Mesoporous
KW - Nitrogen modified
KW - Platinum nanoparticles
UR - https://www.scopus.com/pages/publications/80052491305
U2 - 10.1016/j.jpowsour.2011.07.073
DO - 10.1016/j.jpowsour.2011.07.073
M3 - 文章
AN - SCOPUS:80052491305
SN - 0378-7753
VL - 196
SP - 9299
EP - 9307
JO - Journal of Power Sources
JF - Journal of Power Sources
IS - 22
ER -