TY - JOUR
T1 - Activating Nitrogen-doped Graphene Oxygen Reduction Electrocatalysts in Acidic Electrolytes using Hydrophobic Cavities and Proton-conductive Particles
AU - Singh, Santosh K.
AU - Takeyasu, Kotaro
AU - Homma, Kaito
AU - Ito, Shigeharu
AU - Morinaga, Takashi
AU - Endo, Yuto
AU - Furukawa, Moeko
AU - Mori, Toshiyuki
AU - Ogasawara, Hirohito
AU - Nakamura, Junji
N1 - Funding Information:
This work was supported financially by JSPS KAKENHI (Grant no. 17F17345, 19K15356, and 20H00316) and the Kato Foundation for Promotion of Science (Grant no. KJ‐3031). H.O. thanks the support by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science Program to Ultrafst Catalysis FWP at SLAC National Accelerator Laboratory under Contract No. DE‐AC02‐76SF00515.
Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/12/19
Y1 - 2022/12/19
N2 - Although pyridinic-nitrogen (pyri-N) doped graphene is highly active for the oxygen reduction reaction (ORR) of fuel cells in alkaline media, the activity critically decreases under acidic conditions. We report on how to prevent the deactivation based on the mechanistic understanding that (Formula presented.) governs the ORR kinetics. First, we considered that the deactivation is due to the hydration of pyri-NH+, leading to a lower shift of the redox potential. Introducing the hydrophobic cavity prevented the hydration of pyri-NH+ but inhibited the proton transport. We then increased proton conductivity in the hydrophobic cavity by introducing SiO2 particles coated with ionic liquid polymer/Nafion® which kept the high onset potentials with an increased current density even in acidic media.
AB - Although pyridinic-nitrogen (pyri-N) doped graphene is highly active for the oxygen reduction reaction (ORR) of fuel cells in alkaline media, the activity critically decreases under acidic conditions. We report on how to prevent the deactivation based on the mechanistic understanding that (Formula presented.) governs the ORR kinetics. First, we considered that the deactivation is due to the hydration of pyri-NH+, leading to a lower shift of the redox potential. Introducing the hydrophobic cavity prevented the hydration of pyri-NH+ but inhibited the proton transport. We then increased proton conductivity in the hydrophobic cavity by introducing SiO2 particles coated with ionic liquid polymer/Nafion® which kept the high onset potentials with an increased current density even in acidic media.
UR - http://www.scopus.com/inward/record.url?scp=85143222087&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85143222087&partnerID=8YFLogxK
U2 - 10.1002/anie.202212506
DO - 10.1002/anie.202212506
M3 - Article
C2 - 36240783
AN - SCOPUS:85143222087
SN - 1433-7851
VL - 61
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 51
M1 - e202212506
ER -