TY - JOUR
T1 - Platinum on nitrogen doped graphene and tungsten carbide supports for ammonia electro-oxidation reaction
AU - Siddharth, Kumar
AU - Wang, Yian
AU - Wang, Jing
AU - Xiao, Fei
AU - Nambafu, Gabriel Sikukuu
AU - Shahid, Usman Bin
AU - Yang, Fei
AU - Delmo, Ernest Pahuyo
AU - Shao, Minhua
N1 - Publisher Copyright:
© 2022, Higher Education Press.
PY - 2022/6
Y1 - 2022/6
N2 - Ammonia electrooxidation reaction involving multistep electron-proton transfer is a significant reaction for fuel cells, hydrogen production and understanding nitrogen cycle. Platinum has been established as the best electrocatalyst for ammonia oxidation in aqueous alkaline media. In this study, Pt/nitrogen-doped graphene (NDG) and Pt/tungsten monocarbide (WC)/NDG are synthesized by a wet chemistry method and their ammonia oxidation activities are compared to commercial Pt/C. Pt/NDG exhibits a specific activity of 0.472 mA·cm−2, which is 44% higher than commercial Pt/C, thus establishing NDG as a more effective support than carbon black. Moreover, it is demonstrated that WC as a support also impacts the activity with further 30% increase in comparison to NDG. Surface modification with Ir resulted in the best electrocatalytic activity with Pt-Ir/WC/NDG having almost thrice the current density of commercial Pt/C. This work adds insights regarding the role of NDG and WC as efficient supports along with significant impact of Ir surface modification. [Figure not available: see fulltext.].
AB - Ammonia electrooxidation reaction involving multistep electron-proton transfer is a significant reaction for fuel cells, hydrogen production and understanding nitrogen cycle. Platinum has been established as the best electrocatalyst for ammonia oxidation in aqueous alkaline media. In this study, Pt/nitrogen-doped graphene (NDG) and Pt/tungsten monocarbide (WC)/NDG are synthesized by a wet chemistry method and their ammonia oxidation activities are compared to commercial Pt/C. Pt/NDG exhibits a specific activity of 0.472 mA·cm−2, which is 44% higher than commercial Pt/C, thus establishing NDG as a more effective support than carbon black. Moreover, it is demonstrated that WC as a support also impacts the activity with further 30% increase in comparison to NDG. Surface modification with Ir resulted in the best electrocatalytic activity with Pt-Ir/WC/NDG having almost thrice the current density of commercial Pt/C. This work adds insights regarding the role of NDG and WC as efficient supports along with significant impact of Ir surface modification. [Figure not available: see fulltext.].
KW - Ammonia electro-oxidation reaction
KW - electrocatalyst supports
KW - nitrogen doped graphene
KW - platinum
KW - tungsten carbide
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000765729900002
UR - https://openalex.org/W4220857250
UR - https://www.scopus.com/pages/publications/85125734687
U2 - 10.1007/s11705-021-2130-2
DO - 10.1007/s11705-021-2130-2
M3 - Journal Article
SN - 2095-0179
VL - 16
SP - 930
EP - 938
JO - Frontiers of Chemical Science and Engineering
JF - Frontiers of Chemical Science and Engineering
IS - 6
ER -