Synergistic catalysis of metal-organic framework-immobilized Au-Pd nanoparticles in dehydrogenation of formic acid for chemical hydrogen storage.

نویسندگان

  • Xiaojun Gu
  • Zhang-Hui Lu
  • Hai-Long Jiang
  • Tomoki Akita
  • Qiang Xu
چکیده

Bimetallic Au-Pd nanoparticles (NPs) were successfully immobilized in the metal-organic frameworks (MOFs) MIL-101 and ethylenediamine (ED)-grafted MIL-101 (ED-MIL-101) using a simple liquid impregnation method. The resulting composites, Au-Pd/MIL-101 and Au-Pd/ED-MIL-101, represent the first highly active MOF-immobilized metal catalysts for the complete conversion of formic acid to high-quality hydrogen at a convenient temperature for chemical hydrogen storage. Au-Pd NPs with strong bimetallic synergistic effects have a much higher catalytic activity and a higher tolerance with respect to CO poisoning than monometallic Au and Pd counterparts.

برای دانلود 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

A novel study on the stepwise electrodeposition approach for the synthesis of Pd based nanoparticles, characterization, and their enhanced electrooxidation activities

Herein, a stepwise electrodeposition technique was used to synthesize the Pd based nanoparticles on indium-tin oxide (ITO) electrodes. First of all, Pd nanoparticles were electrodeposited on ITO via one step electrodeposition technique. Furthermore, Au was electrodeposited on Pd. Finally, Co was electrodeposited on Au and Pd electrodeposited ITO electrode via stepwise electrodeposition techniqu...

متن کامل

A novel study on the stepwise electrodeposition approach for the synthesis of Pd based nanoparticles, characterization, and their enhanced electrooxidation activities

Herein, a stepwise electrodeposition technique was used to synthesize the Pd based nanoparticles on indium-tin oxide (ITO) electrodes. First of all, Pd nanoparticles were electrodeposited on ITO via one step electrodeposition technique. Furthermore, Au was electrodeposited on Pd. Finally, Co was electrodeposited on Au and Pd electrodeposited ITO electrode via stepwise electrodeposition techniqu...

متن کامل

An efficient CoAuPd/C catalyst for hydrogen generation from formic acid at room temperature.

Nowadays, searching for the effective hydrogen (H2) storage/ generation materials remains one of the most difficult challenges toward a fuel-cell-based H2 economy as a longterm solution for secure energy in future. Formic acid (FA, HCOOH), a major product of biomass processing with highenergy density, nontoxicity, and excellent stability at room temperature, has recently attracted tremendous re...

متن کامل

Palladium-atom catalyzed formic acid decomposition and the switch of reaction mechanism with temperature.

Formic acid decomposition (FAD) reaction has been an innovative way for hydrogen energy. Noble metal catalysts, especially palladium-containing nanoparticles, supported or unsupported, perform well in this reaction. Herein, we considered the simplest model, wherein one Pd atom is used as the FAD catalyst. With high-level theoretical calculations of CCSD(T)/CBS quality, we investigated all possi...

متن کامل

Mesoporous Silica Supported Pd-MnOx Catalysts with Excellent Catalytic Activity in Room-Temperature Formic Acid Decomposition

For the application of formic acid as a liquid organic hydrogen carrier, development of efficient catalysts for dehydrogenation of formic acid is a challenging topic, and most studies have so far focused on the composition of metals and supports, the size effect of metal nanoparticles, and surface chemistry of supports. Another influential factor is highly desired to overcome the current limita...

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

برای دانلود 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

عنوان ژورنال:
  • Journal of the American Chemical Society

دوره 133 31  شماره 

صفحات  -

تاریخ انتشار 2011