Hee‐Young ParkTae‐Yeol JeonJong Hyun JangSung Jong YooKug‐Seung LeeYoon-Hwan ChoKwang‐Hyun ChoiYong‐Hun ChoNamgee JungYoung‐Hoon ChungYung‐Eun Sung
The hydrogen oxidation reaction activity of sub-monolayer Pt-shell/Pd-core nanoparticles was investigated at a Pt surface concentration of 0 ∼ 5.7%. The nanoparticles were prepared using a colloidal approach. The combination of electrochemical measurements and high resolution-X-ray photoelectron spectroscopy revealed a significant decrease in oxidized Pd atoms (23.4%) with a Pt surface concentration of 1.7% compared with that of Pd/C. X-ray absorption spectroscopy of the Pt LIII edge suggested preferred Pt deposition, which led to more oxidized Pt atoms during Pt shell growth. The exchange current density of the hydrogen oxidation reaction on the electrocatalyst with a Pt surface concentration of 4.9% was 3.5 times higher than that on Pd/C and was comparable with that on Pt surfaces. The changes in hydrogen oxidation reaction apparent enthalpy due to Pt shell growth suggested a rate determining step (RDS) change (Volmer reaction → Tafel reaction) at a Pt surface concentration of 1.7%.
María A. MonteroMaría R. Gennero de ChialvoAbel C. Chialvo
Young‐Woo LeeJin-Yeon LeeDa‐Hee KwakEui-Tak HwangJung Inn SohnKyung‐Won Park
A. LebonAmador García‐FuenteA. VegaF. Aguilera‐Granja
Tao FengMichael GraßYa‐Wen ZhangDerek R. ButcherRuss RenzasZhi LiuJen Y. ChungBongjin Simon MunMiquel SalmerónGábor A. Somorjai
A.S.M. Iftekhar UddinUsman YaqoobKamrul HassanGwiy‐Sang Chung