TY - JOUR
T1 - Active and Stable Oxygen Reduction Catalysts Prepared by Electrodeposition of Platinum on Mo2C at Low Overpotential
AU - Hamo, Eliran Rephael
AU - Saporta, Reut
AU - Rosen, Brian A.
N1 - Publisher Copyright:
©
PY - 2021/3/22
Y1 - 2021/3/22
N2 - Decreasing the cost and improving the durability of polymer electrolyte membrane fuel cell (PEMFC) electrodes are two major unresolved challenges. Electrodeposition of low-dimensional Pt on transition metal carbide supports could be a way to simultaneously address both issues. Synthesis of low-dimensional Pt typically requires expensive equipment or techniques that are difficult to reproduce or scale. An electrodeposition-based technique to accomplish this goal is therefore highly desirable. The strong adhesion energy between Pt and the C sites on the α-Mo2C surface suggests that an electrochemical technique could be exploited for this purpose. Here, PtCl62- was electrodeposited onto an α-Mo2C support at low and high overpotentials (η). A dramatic increase in the electrochemical surface area and the mass activity of the oxygen reduction reaction (ORR) was observed when Pt was deposited at low overpotentials (+8 and +18 mV vs SCE) as compared to high overpotentials (-67 and -92 mV vs SCE). Indeed, catalysts prepared in the low-overpotential region achieved an ORR mass activity of 275 A/gPt and broke the linear relationship between mass activity and loading typically exhibited by these materials. Furthermore, catalysts prepared in the low-overpotential region exhibited superior stability out to 5000 cycles in an accelerated stress test (AST) as compared to samples prepared at higher overpotentials or by chemical reduction of Pt onto α-Mo2C and carbon supports.
AB - Decreasing the cost and improving the durability of polymer electrolyte membrane fuel cell (PEMFC) electrodes are two major unresolved challenges. Electrodeposition of low-dimensional Pt on transition metal carbide supports could be a way to simultaneously address both issues. Synthesis of low-dimensional Pt typically requires expensive equipment or techniques that are difficult to reproduce or scale. An electrodeposition-based technique to accomplish this goal is therefore highly desirable. The strong adhesion energy between Pt and the C sites on the α-Mo2C surface suggests that an electrochemical technique could be exploited for this purpose. Here, PtCl62- was electrodeposited onto an α-Mo2C support at low and high overpotentials (η). A dramatic increase in the electrochemical surface area and the mass activity of the oxygen reduction reaction (ORR) was observed when Pt was deposited at low overpotentials (+8 and +18 mV vs SCE) as compared to high overpotentials (-67 and -92 mV vs SCE). Indeed, catalysts prepared in the low-overpotential region achieved an ORR mass activity of 275 A/gPt and broke the linear relationship between mass activity and loading typically exhibited by these materials. Furthermore, catalysts prepared in the low-overpotential region exhibited superior stability out to 5000 cycles in an accelerated stress test (AST) as compared to samples prepared at higher overpotentials or by chemical reduction of Pt onto α-Mo2C and carbon supports.
KW - catalysts
KW - fuel cells
KW - oxygen reduction reaction
KW - platinum
KW - transition metal carbides
KW - underpotential deposition
UR - http://www.scopus.com/inward/record.url?scp=85103377381&partnerID=8YFLogxK
U2 - 10.1021/acsaem.0c02615
DO - 10.1021/acsaem.0c02615
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AN - SCOPUS:85103377381
SN - 2574-0962
VL - 4
SP - 2130
EP - 2137
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 3
ER -