Direct Integration of Strained-Pt Catalysts into Proton-Exchange-Membrane Fuel Cells with Atomic Layer Deposition.
Shicheng XuZhaoxuan WangSam DullYunzhi LiuDong Un LeeJuan S Lezama PachecoMarat OrazovPer Erik VullumAnup Lal DadlaniOlga VinogradovaPeter SchindlerQizhan TamThomas D SchladtJonathan E MuellerSebastian KirschGerold HuebnerDrew HigginsJan TorgersenVenkatasubramanian ViswanathanThomas Francisco JaramilloFritz B PrinzPublished in: Advanced materials (Deerfield Beach, Fla.) (2021)
The design and fabrication of lattice-strained platinum catalysts achieved by removing a soluble core from a platinum shell synthesized via atomic layer deposition, is reported. The remarkable catalytic performance for the oxygen reduction reaction (ORR), measured in both half-cell and full-cell configurations, is attributed to the observed lattice strain. By further optimizing the nanoparticle geometry and ionomer/carbon interactions, mass activity close to 0.8 A mgPt -1 @0.9 V iR-free is achievable in the membrane electrode assembly. Nevertheless, active catalysts with high ORR activity do not necessarily lead to high performance in the high-current-density (HCD) region. More attention shall be directed toward HCD performance for enabling high-power-density hydrogen fuel cells.