4.8 Article

Ultrahigh Pt-Mass-Activity Hydrogen Evolution Catalyst Electrodeposited from Bulk Pt

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 32, Issue 20, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202112207

Keywords

electrochemical deposition; hydrogen evolution; hydrogen spillover; Pt; tungsten oxides

Funding

  1. Natural Science Foundation Program of Beijing [2202031, 2174079, 2162027]
  2. National Natural Science Foundation Program of China [51574030, 51574029, 51604240]
  3. Key Research and Development Project of Hebei Province [20311001D]
  4. Fundamental Research Funds for the Central Universities [FRF-IDRY-20-022, QNXM20210046, FRF-TP-19-015A3, FRF-TP-19-003C2, FRF-TP-17-034A2]
  5. USTB-NTUT Joint Research Program [06310061]
  6. Scientific Research Foundation of Hunan Provincial Education Department [18A196]
  7. Postdoctor Research Foundation of Shunde Graduate School of University of Science and Technology Beijing [2020BH014]

Ask authors/readers for more resources

This study reports on a three-component heterostructured hydrogen evolution reaction (HER) catalyst with ultra-high Pt mass activity. The catalyst consists of hollow PtCu alloy nanospheres supported on an array of WO3 on Cu foam. By utilizing the contamination from the Pt counter electrode, the authors were able to activate low-HER-activity materials, maximizing the utilization of Pt. The resulting catalyst exhibits ultrahigh Pt mass activity, outperforming commercial Pt/C catalysts and some state-of-the-art Pt-single-atom catalysts.
Maximizing the Pt utilization is important for the widescale implementation of Pt-based hydrogen evolution reaction (HER) electrocatalysts, owing to the scarcity of Pt. Here, three-component heterostructured HER catalysts with ultrahigh Pt mass activity in which hollow PtCu alloy nanospheres are supported on an array of WO3 on Cu foam, are reported. It has been pointed out that the use of Pt counter electrode in a three-electrode configuration in evaluating catalysts' HER performances in acidic media carries the risk of contaminating the working electrode in previous reports. Here, the authors rationally utilize this contaminating to activate low-HER-activity materials, maximizing the Pt utilization. As a result, ultrahigh Pt mass activity is achieved, that is 1.35 and 10.86 A mg(Pt)(-1) at overpotentials of 20 and 100 mV, respectively, 27 and 13 times higher than those of commercial Pt/C catalysts, outperforming some state-of-the-art Pt-single-atom catalysts. The hollow sphere structure and PtCu alloying increase the number and reactivity of active sites. Density function calculations and electrochemical experiments reveal that the synergy between WO3 and Pt is also responsible for the high HER activity where the hydrogen spillover effect triggers the Volmer-Heyrovsky mechanism and promotes the rapid removal of H* from Pt to re-expose the active sites.

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