TY - JOUR
T1 - Three dimensional few-layer porous carbon nanosheets towards oxygen reduction
AU - Zhang, Jian
AU - Zhang, Chenyu
AU - Zhao, Yufeng
AU - Amiinu, Ibrahim Saana
AU - Zhou, Huang
AU - Liu, Xiaobo
AU - Tang, Yongfu
AU - Mu, Shichun
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017
Y1 - 2017
N2 - Novel three dimensional (3D) porous carbon nanosheets with few layers are successfully prepared using intrinsically porous cellulose as carbon matrix only by means of calcination and KOH activation. Further, the N-doped 3D carbon nanosheets show high density of pyridinic N and extremely high specific surface area (1756 m2 g−1). As oxygen reduction catalyst, they possess an outperformed onset (E0 = −0.03 V) and half-wave (E1/2 = −0.17 V) potential compared with the platinum (Pt) electrocatalyst (E0 = −0.05 V, E1/2 = −0.2 V) in an alkaline system. In addition, excellent electrochemical stability as well as improved CO poisoning resistance and suppressed methanol crossover relative to Pt is also obtained. In an acid system, the catalyst also exhibits good activity and higher durability than Pt/C. Significantly, when used as a catalyst of the air electrode for Zn–air batteries, it demonstrates a higher peak power density of 208 mW cm−2 and a voltage plateau at the controlled discharge current density compared to the commercial Pt/C electrode. This simple and scalable approach provides a direct route to synthesize low cost and highly efficient electrocatalysts from biomass without addition of extra metal catalysts.
AB - Novel three dimensional (3D) porous carbon nanosheets with few layers are successfully prepared using intrinsically porous cellulose as carbon matrix only by means of calcination and KOH activation. Further, the N-doped 3D carbon nanosheets show high density of pyridinic N and extremely high specific surface area (1756 m2 g−1). As oxygen reduction catalyst, they possess an outperformed onset (E0 = −0.03 V) and half-wave (E1/2 = −0.17 V) potential compared with the platinum (Pt) electrocatalyst (E0 = −0.05 V, E1/2 = −0.2 V) in an alkaline system. In addition, excellent electrochemical stability as well as improved CO poisoning resistance and suppressed methanol crossover relative to Pt is also obtained. In an acid system, the catalyst also exhibits good activity and higher durability than Pt/C. Significantly, when used as a catalyst of the air electrode for Zn–air batteries, it demonstrates a higher peak power density of 208 mW cm−2 and a voltage plateau at the controlled discharge current density compared to the commercial Pt/C electrode. This simple and scalable approach provides a direct route to synthesize low cost and highly efficient electrocatalysts from biomass without addition of extra metal catalysts.
KW - Biomass
KW - Carbon nanosheet
KW - Cellulose
KW - Nitrogen doping
KW - Oxygen reduction
UR - https://www.scopus.com/pages/publications/85018506725
U2 - 10.1016/j.apcatb.2017.04.038
DO - 10.1016/j.apcatb.2017.04.038
M3 - Article
AN - SCOPUS:85018506725
SN - 0926-3373
VL - 211
SP - 148
EP - 156
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -