TY - JOUR
T1 - PdAgRu nanoparticles on polybenzimidazole wrapped CNTs for electrocatalytic formate oxidation
AU - Gebremariam, Tesfaye Tadesse
AU - Chen, Fuyi
AU - Kou, Bo
AU - Guo, Longfei
AU - Pan, Bowei
AU - Wang, Qiao
AU - Li, Zhen
AU - Bian, Weiqi
N1 - Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/9/10
Y1 - 2020/9/10
N2 - Direct formate fuel cells (DFFCs) have received great interest as potential candidates of power sources, and their viability primarily relies on exploration of efficient formate oxidation reaction (FOR) catalysts. Herein, we have prepared PdAgRu nanoparticles supported on polybenzimidazole wrapped carbon nanotubes (pCNTs), Pd6Ag3Ru1/pCNTs catalyst which displays remarkable mass activity of 4.7 A mgPd−1 and maintains current density of 0.71 A mg−1 after 5400 s of chronoamperometry test, which is 2.1 and 26.7 times better than that of commercial Pd/C catalyst, respectively. The performance improvement is attributed to delicately designed components, polybenzimidazole layer serves as hydroxide transporter, carbon nanotubes function as electron conductive path, Ag weakens binding strength of adsorbed hydrogen (Hads) on Pd, and Ru promotes the formation of hydroxyl species. Impressively, when the upper limit potential of cyclic voltammetry is enlarged into Ag redox region, the FOR activity remarkably increases, the mass activities are 4.30, 4.7 and 5.12 A mgPd−1at 1.1, 1.3 and 1.5 V, respectively. The closer examination of x-ray photoelectron spectroscopy (XPS) spectra reveal the co-existence of mixed Pd(0)/Pd(II) and Ag(0)/Ag(I) state on the catalyst surface. The amount of Pd(0) and Ag(I) state increase with increasing upper limit potential, which is attributed to surface restructuration.
AB - Direct formate fuel cells (DFFCs) have received great interest as potential candidates of power sources, and their viability primarily relies on exploration of efficient formate oxidation reaction (FOR) catalysts. Herein, we have prepared PdAgRu nanoparticles supported on polybenzimidazole wrapped carbon nanotubes (pCNTs), Pd6Ag3Ru1/pCNTs catalyst which displays remarkable mass activity of 4.7 A mgPd−1 and maintains current density of 0.71 A mg−1 after 5400 s of chronoamperometry test, which is 2.1 and 26.7 times better than that of commercial Pd/C catalyst, respectively. The performance improvement is attributed to delicately designed components, polybenzimidazole layer serves as hydroxide transporter, carbon nanotubes function as electron conductive path, Ag weakens binding strength of adsorbed hydrogen (Hads) on Pd, and Ru promotes the formation of hydroxyl species. Impressively, when the upper limit potential of cyclic voltammetry is enlarged into Ag redox region, the FOR activity remarkably increases, the mass activities are 4.30, 4.7 and 5.12 A mgPd−1at 1.1, 1.3 and 1.5 V, respectively. The closer examination of x-ray photoelectron spectroscopy (XPS) spectra reveal the co-existence of mixed Pd(0)/Pd(II) and Ag(0)/Ag(I) state on the catalyst surface. The amount of Pd(0) and Ag(I) state increase with increasing upper limit potential, which is attributed to surface restructuration.
KW - Carbon nanotube
KW - Formate oxidation reaction
KW - Fuel cell
KW - PdAgRu
KW - Polybenzimidazole
UR - http://www.scopus.com/inward/record.url?scp=85087492268&partnerID=8YFLogxK
U2 - 10.1016/j.electacta.2020.136678
DO - 10.1016/j.electacta.2020.136678
M3 - 文章
AN - SCOPUS:85087492268
SN - 0013-4686
VL - 354
JO - Electrochimica Acta
JF - Electrochimica Acta
M1 - 136678
ER -