Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseОткрытый API экосистемы
Статья

Heterogeneous Cu–Pd binary interface boosts stability and mass activity of atomic Pt clusters in the oxygen reduction reaction

Hsin‐Yi Tiffany ChenDepartment of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan. [email protected]Jyh‐Pin ChouInstitute for Solid State Physics and Optics, Wigner Research Centre for Physics, Hungarian Academy of Sciences, POB 49, Budapest, HungaryCheng-Yang LinDepartment of Electrical Engineering & Institute of Electronic Engineering, National Tsing Hua University, Hsinchu 30013, TaiwanChih‐Wei HuDepartment of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, TaiwanYa‐Tang YangDepartment of Electrical Engineering & Institute of Electronic Engineering, National Tsing Hua University, Hsinchu 30013, TaiwanTsan‐Yao ChenDepartment of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan
2017en
ABI

Аннотация

A ternary metallic CuPdPt nanocatalyst (NC) is synthesized using a wet chemical reduction method, which is sequentially designed, in the presence of acid treated carbon nanotubes. This NC is a nanocrystal with a configuration of a Cu@Pd core and atomic Pt clusters (∼9 wt%) on the top (Cu@Pd/Pt). A residual current of 92.6%, 5.2 times higher than that of commercial Pt catalysts (at 0.85 V vs. RHE), is retained after 40 000 cycles of an accelerated degradation test (ADT). Atomic and electronic structure analyses show that such exclusive stability mainly results from electron localization at Pt clusters in heterogeneous interfaces of the Cu-Pd core. Most importantly, we develop a robust ternary NC, which shows outstanding MA, superior chemical durability, and ∼90 wt% lower Pt loading than commercial Pt NCs in the oxygen reduction reaction.

Перевод пока недоступен

Идентификаторы

Цитирования и источники

Цитирований: 3Использованных источников: 0