TY - JOUR
T1 - Trace cobalt-inserted platinum lattice gap to enable bifunctional oxygen electrocatalysis
AU - Yang, Jie
AU - Song, Shilong
AU - Chen, Zhanwei
AU - Zhang, Bo
AU - Guo, Yuyu
AU - Guo, Ying
AU - Zhang, Hepeng
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/1/7
Y1 - 2025/1/7
N2 - Platinum-based materials are generally considered efficient oxygen reduction reaction (ORR) electrocatalysts but show poor performance for oxygen evolution reaction (OER), which limits their applications in zinc-air batteries (ZABs). Therefore, it is of great importance to develop highly effective bifunctional ORR and OER Pt-based electrocatalysts. Herein, a Co atom-inserted Pt lattice gap electrocatalyst (Co-Pt@Fe-N-C) was constructed. Experimental and theoretical calculations illustrated that the insertion of Co caused the lattice expansion of Pt nanocrystal and increased the Pt electron density, thereby upshifting the Pt d-band center. Benefiting from this, the interactions between Pt active sites and ORR/OER intermediates were stabilized, which improved the ORR/OER electrocatalytic performances. A half-potential of 0.89 V vs. RHE for ORR and narrow ORR/OER potential gap (0.75 V) were achieved, and Co-Pt@Fe-N-C-based ZABs exhibited a stable open circuit potential of 1.52 V, peak power density of 151 mW cm−2, and over 850 hours of stability. Thus, our work has significant potential to guide future research works on the design of effective Pt-based ORR/OER bifunctional electrocatalysts and ZABs.
AB - Platinum-based materials are generally considered efficient oxygen reduction reaction (ORR) electrocatalysts but show poor performance for oxygen evolution reaction (OER), which limits their applications in zinc-air batteries (ZABs). Therefore, it is of great importance to develop highly effective bifunctional ORR and OER Pt-based electrocatalysts. Herein, a Co atom-inserted Pt lattice gap electrocatalyst (Co-Pt@Fe-N-C) was constructed. Experimental and theoretical calculations illustrated that the insertion of Co caused the lattice expansion of Pt nanocrystal and increased the Pt electron density, thereby upshifting the Pt d-band center. Benefiting from this, the interactions between Pt active sites and ORR/OER intermediates were stabilized, which improved the ORR/OER electrocatalytic performances. A half-potential of 0.89 V vs. RHE for ORR and narrow ORR/OER potential gap (0.75 V) were achieved, and Co-Pt@Fe-N-C-based ZABs exhibited a stable open circuit potential of 1.52 V, peak power density of 151 mW cm−2, and over 850 hours of stability. Thus, our work has significant potential to guide future research works on the design of effective Pt-based ORR/OER bifunctional electrocatalysts and ZABs.
UR - http://www.scopus.com/inward/record.url?scp=85216219508&partnerID=8YFLogxK
U2 - 10.1039/d4ta07260j
DO - 10.1039/d4ta07260j
M3 - 文章
AN - SCOPUS:85216219508
SN - 2050-7488
VL - 13
SP - 6020
EP - 6026
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 8
ER -