Ultra-high-performance core–shell structured Ru@Pt/C catalyst prepared by a facile pulse electrochemical deposition method

نویسندگان

  • Dan Chen
  • Yuexia Li
  • Shijun Liao
  • Dong Su
  • Huiyu Song
  • Yingwei Li
  • Lijun Yang
  • Can Li
چکیده

Core-shell structured catalysts, made by placing either a monolayer or a thin layer of a noble metal on relatively cheap core-metal nanoparticles, are fascinating and promising fuel cell catalysts due to their high utilization of noble metals. Here, we report our development of a core-shell structured catalyst, Ru@Pt/C, generated by a novel and facile pulse electrochemical deposition (PED) approach. We demonstrate that compared with a commercial Pt/C catalyst, this novel catalyst achieves over four times higher mass activity towards the anodic oxidation of methanol, and 3.6 times higher mass activity towards the cathodic reduction of oxygen. Importantly, we find that the intrinsic activity of Pt in this Ru@Pt/C catalyst is doubled due to the formation of the core-shell structure. The catalyst also shows superior stability: even after 2000 scans, it still retains up to 90% of the peak current. Our findings demonstrate that this novel PED approach is a promising method for preparing high-performance core-shell catalysts for fuel cell applications.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Engineering Ru@Pt Core-Shell Catalysts for Enhanced Electrochemical Oxygen Reduction Mass Activity and Stability

Improving the performance of oxygen reduction reaction (ORR) electrocatalysts is essential for the commercial efficacy of many renewable energy technologies, including low temperature polymer electrolyte fuel cells (PEFCs). Herein, we report highly active and stable carbon-supported Ru@Pt core-shell nanoparticles (Ru@Pt/C) prepared by a wet chemical synthesis technique. Through rotating disc el...

متن کامل

Ag/Pt Core-Shell Nanoparticles on Graphene Nanocomposite for Effective Anodic Fuels Electro-oxidation

The nanocomposite consists of the Ag as a core and Pt as shell on the surface of graphene nanosheets (Ag/Pt-G) was synthesized with a simple method and used as a novel electrochemical platform for an efficient catalyst for oxidation of the ethanol, methanol and formic acid. The morphology and electrochemical properties of Ag/Pt-G nanocomposite were investigated by TEM, X-ray diffraction, and vo...

متن کامل

Ni@Pt core-shell nanoparticles as an improved electrocatalyst for ethanol electrooxidation in alkaline media

Core-shell nanostructures are emerging as more important materials than alloy nanostructures and have much more interesting potential applications in various fields. In this work, we demonstrated the fast and facile synthesis of core-shell nanoparticles consisting of Pt thin layer as the shell and Ni nanoparticles as the cores. The described method herein is suitable for large-scale and low-cos...

متن کامل

Core–shell titanium dioxide /carbon nanofibers decorated nickel nanoparticles as supports for electrocatalytic oxidation of ethanol

Abstract Recently alcohol fuel cells has been increased consideration because of their environmental friendliness, high energy conversion efficiency and low emissions. Many effort have been made to improve the electro-oxidation performance of alcohols such as methanol, ethanol and propanol. In this work, a new method for ethanol oxidation based on core–shell titanium dioxide / carbon nanofib...

متن کامل

Using the Palladium as core and Platinum as shell for ORR

In this work, electrocatalyst with core-shell structure (Pd as core and Pt as shell on VulcanXC-72R) was synthesis. Not only this structure can reduce the amount of platinum but it also can increase the gas diffusion electrode (GDE) performance in cathode reaction (Oxygen Reduction Reaction or ORR) of polymer electrolyte membrane fuel cell (PEMFC). To this meaning, one series of electrocatalyst...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2015