4.6 Article

Bifunctional networked Ag/AgPd core/shell nanowires for the highly efficient dehydrogenation of formic acid and subsequent reduction of nitrate and nitrite in water

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 11, Pages 4611-4616

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta00600h

Keywords

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Funding

  1. National Natural Science Foundation of China [51571072]
  2. Fundamental Research Funds for the Central Universities [AUGA5710012715]
  3. China Postdoctoral Science Foundation [2015M81436]
  4. Heilongjiang Postdoctoral Science Foundation [LBH-Z15065]

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Nitrate (NO3-) and nitrite (NO2-) pollution in water has increasingly become a serious environmental concern. The catalytic reduction of NO3- and NO2- to harmless N-2 by a reducing agent is considered to be one of the most promising methods to remove NO3- and NO2- from water. Herein, we report the one-pot synthesis of networked Ag/AgPd core/shell nanowires (CS-NWs) via seed-mediated growth in polyol solution. The shell thickness of the networked Ag/AgPd CS-NWs can be readily controlled by tuning the amount of precursors. The networked Ag/AgPd CS-NWs with a 0.9 nm shell thickness exhibited the highest activity towards the dehydrogenation catalysis of FA with an initial TOF of 1400 h(-1) at 50 degrees C, and the highest selectivity for the catalysis of NO3- and NO2- to N-2 in water and at room temperature. Their enhanced bifunctional catalytic performance could be attributed to more efficient electron transfer from PVPI and Ag to Pd. This work demonstrates a new way to prepare bifunctional nanocatalysts for the removal of NO3- and NO2- from water using FA as the in situ hydrogen source.

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