第一作者: |
Cao, LJ (Cao, Lijuan); Wang, XL (Wang, Xilong); Yang, C (Yang, Chen); Lu, JJ (Lu, Jiajia); Shi, XY (Shi, Xiaoyue); Zhu, HW (Zhu, Hongwei); Liang, HP (Liang, Han-Pu); |
联系作者: |
Cao, LJ (Cao, Lijuan); Wang, XL (Wang, Xilong); Yang, C (Yang, Chen); Lu, JJ (Lu, Jiajia); Shi, XY (Shi, Xiaoyue); Zhu, HW (Zhu, Hongwei); Liang, HP (Liang, Han-Pu); |
发表年度: |
2021 |
期: |
1 |
卷: |
9 |
页: |
189-196 |
摘要: |
The highly active bimetallic single-atom electrocatalysts are desirable for the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) but remain challenging. Herein, Fe/Pt single-atom bifunctional electrocatalysts (Fe1Pt1/NC) are initially fabricated by nitrogen doping during the pyrolysis of porphyra and adsorbed urea at high temperature with subsequent nitrogen anchoring of Pt4+ in aqueous solution with the as-synthesized nitrogen-doped carbon. The as-synthesized Fe1Pt1/NC electrocatalysts have been intensively characterized by HAADF-STEM, XAFS, HRTEM, XRD, and Raman analysis. Particularly, the Fe1Pt1/NC presents excellent electrocatalytic activity toward HER, with relatively low overpotential of 27 mV at 10 mA cm(-2) and small Tafel slopes of 28 mV Furthermore, the Fe1Pt1/NC electrocatalyst possesses superior ORR activity with an onset potential of 1.04 V and half-wave potential of 0.91 V. This work provides a feasible way to synthesize electrocatalysts with abundant single-atom sites using renewable biomass as a precursor. |
刊物名称: |
ACS SUSTAINABLE CHEMISTRY & ENGINEERING |
影响因子: |
6.97 |
全文链接: |
https://pubs.acs.org/doi/10.1021/acssuschemeng.0c06558 |