2192
(Invited) Development of Highly Active and Durable Hybrid Compressive Platinum for Polymer Electrolyte Membrane (PEM) Fuel Cells at USC

Tuesday, 15 May 2018: 17:00
Room 603 (Washington State Convention Center)
B. N. Popov (University of South Carolina), T. Kim (Chungnam National University,), and W. S. Jung (University of South Carolina)
The overall objective of this work was development proton exchange membrane (PEM) fuel cell catalysts for the oxygen reduction reaction (ORR) having ultra-low Pt loading with low cost, high performance and durability. The approach was based on development of a catalyst bridging the current platinum group metal (PGM) catalyst technology and the non-platinum cathode catalyst developed at USC. To balance the cost and the limited supply of platinum, the ultra-low platinum alloy project at (USC) developed highly stable and kinetically-activated carbon composite supports (A-CCS) as well as highly-active and stable hybrid cathode catalyst (HCC), Pt*/A-CCS (Pt* = Compressive Pt-lattice catalyst) that retain their activity after accelerated testing to simulate startup/shutdown and drive cycle potential cycling thus accomplishing the DOE 2017 targets. The HCC technology is based on a two-step patented process.1-10 In order to develop a hybrid catalysts, in the first step, the following major constraints in the PEM fuel cells interfaces were addressed : (a) chemical and electrochemical stability of the support at high potentials, low pH and high temperature and (b) the support onset potential and kinetic activity for oxygen reduction reaction to be similar to that of a platinum catalyst. To accomplish these requirements, the A-CCS was synthesized with optimized: (i) BET surface area, porosity, pore-size and distribution and active sties for ORR (ii) hydrophilic/hydrophobic ratio, (iii) structural properties (amorphous/crystalline ratio). In the second step, compressive Pt-lattice catalyst (Pt*) was synthesized through a USC-developed annealing procedure that controls the particle size during annealing and forms monolayers of Pt* by diffusing Co atoms present in the support into Pt which is deposited on A-CCS support. In this step, Pt/Pt*-support interaction was optimized through inclusion of active surface functional groups, and through optimization of transition metal content in the alloy necessary for the formation of compressive Pt-lattice catalyst. The Pt*/A-CCS shows high mass activity (0.41 A/mg Pt), excellent support stability, and enhanced catalyst durability under accelerated stress test (AST) conditions. Initial mass activity, mass activity and ECSA loss after 30K cycles (0.6 -1.0 V- catalyst durability), potential loss after 30 K cycles (0.6-1.0-catalyst durability), potential loss after 5 K cycles (1.0-1.5V-support stability) and mass activity and ECSA loss after 5 k cycles (1.0-1.5V-support stability) will be compared in the presentation with 2020 DOE Technical targets for PEM catalyst and supports.

References

  1. Ákos Kriston, Andreas Pfrang, Branko N. Popov, and L. Boon-Brett, “Development of a Full Layer Pore-Scale Model for the Simulation of Electro-Active Material Used in Power Sources,” Electrochem. Soc., 161 (2015) E3235-E3247.
  2. Kim, T. Xie, W.S. Jung, F. Gadala-Maria, P. Ganesan, B.N. Popov, Development of Catalytically Active and Highly Stable Catalyst Supports for Polymer Electrolyte Membrane Fuel Cells, J. Power Sources, 273, (2015) 761-774.
  3. Wonsuk Jung, Tianyuan Xie, Taekeun Kim, Prabhu Ganesan, Branko N. Popov, Highly Active and Durable Co-Doped Pt/CCC Cathode Catalyst for Polymer Electrolyte Membrane Fuel Cells, Acta, 167, (2015) 1-12.
  4. Takeun Kim , Branko N. Popov, Development of highly-active and stable Pt/C Catalyst for Polymer Electrolyte Membrane Fuel Cells Under Simulated Start up/Shut Down Cycling, International Journal of Hydrogen Energy, 41, (2016) 1328-1336.
  5. N. Popov, Jong-Won Lee, Sehkyu Park, Chapter Electrocatalyst for Low Temperature Fuel Cells,” John Willey and Sons, VCH, RE 9783527341320 (2016).
  6. Taekeun Kim, Tianyuan Xie, Won Suk Jung , Branko N. Popov, Development of Ultra-low Highly Active and Durable Hybrid Compressive Platinum Lattice Cathode Catalyst for Polymer Electrolyte Membrane Fuel Cells, International Journal of Hydrogen Energy, 42, (2017), 12507-12520.
  7. Won Suk Jung, Branko N. Popov, Improved Durability of Pt Catalyst Supported on N-doped Mesoporous Graphitized Carbon for Oxygen Reduction Reaction in Polymer Electrolyte Membrane Fuel Cells, Carbon, 122 (2017) 746-755.
  8. Won Suk Jung and Branko N. Popov, New Method to Synthesize Highly Active and Durable Chemically Ordered fct-PtCo Cathode Catalyst for PEMFC’s, ACS Appl. Mater. Interfaces, (2017), 9, 23879-23686.
  9. Won Suk Jung and Branko N. Popov, Hybrid cathode catalyst with Synergistic effect Between Carbon Composite Catalyst and Pt for Ultra –low Pt Loading in PEMFC’s, Catalysis Today, 295, (2017) 65-74.\
  10. Won Suk Jung and Branko N. Popov, Effect of Pretreatment on Durability of fct-Structured Pt-Based Alloy Catalyst for Oxygen Reduction Reaction in Polymer Electrolyte Membrane Fuel Cells, ACS Sustainable Chem. and Eng, (09)(2017) DOI: 10.1021.