TY - JOUR
T1 - Robust MOF-253-derived N-doped carbon confinement of Pt single nanocrystal electrocatalysts for oxygen evolution reaction
AU - Monestel, Hellen Gabriela Rivera
AU - Amiinu, Ibrahim Saana
AU - González, Andrés Alvarado
AU - Pu, Zonghua
AU - Mousavi, Bibi Maryam
AU - Mu, Shichun
N1 - Publisher Copyright:
© 2020 Dalian Institute of Chemical Physics, the Chinese Academy of Sciences
PY - 2020/5
Y1 - 2020/5
N2 - Although carbon-supported platinum (Pt/C) is still considered the most active electrocatalyst for hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR), its applications in metal-air batteries as a cathode catalyst, or for oxygen generation via water splitting electrolysis as an anode catalyst is mainly constrained by the insufficient kinetic activity and stability in the oxygen evolution reaction (OER). Here, MOF-253-derived nitrogen-doped carbon (N/C)-confined Pt single nanocrystals (Pt@N/C) have been synthesized and shown to be efficient catalysts for the OER. Even with low Pt mass loading of 6.1 wt% (Pt@N/C-10), the catalyst exhibits greatly improved activity and long-time stability as an efficient OER catalyst. Such high catalytic performance is attributed to the core-shell structure relationship, in which the active N-doped-C shell not only provides a protective shield to avoid rapid Pt nanocrystal oxidation at high potentials and inhibits the Pt migration and agglomeration, but also improves the conductivity and charge transfer kinetics.
AB - Although carbon-supported platinum (Pt/C) is still considered the most active electrocatalyst for hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR), its applications in metal-air batteries as a cathode catalyst, or for oxygen generation via water splitting electrolysis as an anode catalyst is mainly constrained by the insufficient kinetic activity and stability in the oxygen evolution reaction (OER). Here, MOF-253-derived nitrogen-doped carbon (N/C)-confined Pt single nanocrystals (Pt@N/C) have been synthesized and shown to be efficient catalysts for the OER. Even with low Pt mass loading of 6.1 wt% (Pt@N/C-10), the catalyst exhibits greatly improved activity and long-time stability as an efficient OER catalyst. Such high catalytic performance is attributed to the core-shell structure relationship, in which the active N-doped-C shell not only provides a protective shield to avoid rapid Pt nanocrystal oxidation at high potentials and inhibits the Pt migration and agglomeration, but also improves the conductivity and charge transfer kinetics.
KW - Carbon confinement
KW - Electrocatalyst
KW - MOF-253
KW - Oxygen evolution reaction
KW - Pt
UR - https://www.scopus.com/pages/publications/85078217857
U2 - 10.1016/S1872-2067(19)63488-1
DO - 10.1016/S1872-2067(19)63488-1
M3 - Article
AN - SCOPUS:85078217857
SN - 1872-2067
VL - 41
SP - 839
EP - 846
JO - Chinese Journal of Catalysis
JF - Chinese Journal of Catalysis
IS - 5
ER -