TY - JOUR
T1 - Electronegativity- induced cobalt-doped platinum hollow nanospheres with high CO tolerance for efficient methanol oxidation reaction
AU - Yang, Hu
AU - Li, Chang
AU - Lü, Linzhe
AU - Li, Zhuogen
AU - Zhang, Shiqi
AU - Huang, Zheng
AU - Ma, Rui
AU - Liu, Sisi
AU - Ge, Ming
AU - Zhou, Wei
AU - Yuan, Xiaolei
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/1/15
Y1 - 2025/1/15
N2 - Although Platinum (Pt)-based alloys have garnered significant interest within the realm of direct methanol fuel cells (DMFCs), there still exists a notable dearth in the exploration of the catalytic behavior of the liquid fuels on well-defined active sites and unavoidable Pt poisoning because of the adsorbed CO species (COads). Here, we propose an electronegativity-induced electronic redistribution strategy to optimize the adsorption of crucial intermediates for the methanol oxidation reaction (MOR) by introducing the Co element to form the PtCo alloys. The optimal PtCo hollow nanospheres (HNSs) exhibit excellent high-quality activity of 3.27 A mgPt−1, which is 11.6 times and 13.1 times higher than that of Pt/C and pure Pt, respectively. The in-situ Fourier transform infrared reflection spectroscopy validates that electron redistribution could weak CO adsorption, and subsequently decrease the CO poisoning adjacent the Pt active sites. Theoretical simulations result show that the introduction of Co optimize surface electronic structure and reduce the d-band center of Pt, thus optimized the adsorption behavior of COads. This study not only employs a straightforward method for the preparation of Pt-based alloys but also delineates a pathway toward designing advanced active sites for MOR via electronegativity-induced electronic redistribution.
AB - Although Platinum (Pt)-based alloys have garnered significant interest within the realm of direct methanol fuel cells (DMFCs), there still exists a notable dearth in the exploration of the catalytic behavior of the liquid fuels on well-defined active sites and unavoidable Pt poisoning because of the adsorbed CO species (COads). Here, we propose an electronegativity-induced electronic redistribution strategy to optimize the adsorption of crucial intermediates for the methanol oxidation reaction (MOR) by introducing the Co element to form the PtCo alloys. The optimal PtCo hollow nanospheres (HNSs) exhibit excellent high-quality activity of 3.27 A mgPt−1, which is 11.6 times and 13.1 times higher than that of Pt/C and pure Pt, respectively. The in-situ Fourier transform infrared reflection spectroscopy validates that electron redistribution could weak CO adsorption, and subsequently decrease the CO poisoning adjacent the Pt active sites. Theoretical simulations result show that the introduction of Co optimize surface electronic structure and reduce the d-band center of Pt, thus optimized the adsorption behavior of COads. This study not only employs a straightforward method for the preparation of Pt-based alloys but also delineates a pathway toward designing advanced active sites for MOR via electronegativity-induced electronic redistribution.
KW - Electronegativity
KW - Membrane electrode assembly
KW - Methanol oxidation reaction
KW - PtCo hollow nanospheres
UR - http://www.scopus.com/inward/record.url?scp=85203868789&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2024.09.111
DO - 10.1016/j.jcis.2024.09.111
M3 - 文章
C2 - 39298982
AN - SCOPUS:85203868789
SN - 0021-9797
VL - 678
SP - 300
EP - 308
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -