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A hierarchically porous nickel-copper phosphide nano-foam for efficient electrochemical splitting of water

  • Li Wei
  • , Kunli Goh
  • , Özgür Birer
  • , H. Enis Karahan
  • , Jian Chang
  • , Shengli Zhai
  • , Xuncai Chen
  • , Yuan Chen*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • University of Sydney
  • Nanyang Technological University
  • Koc University

Araştırma sonucu: Dergiye katkıMakalebilirkişi

122 Atıf (Scopus)

Özet

Electrochemical splitting of water to produce oxygen (O2) and hydrogen (H2) through a cathodic hydrogen evolution reaction (HER) and an anodic oxygen evolution reaction (OER) is a promising green approach for sustainable energy supply. Here we demonstrated a porous nickel-copper phosphide (NiCuP) nano-foam as a bifunctional electrocatalyst for highly efficient total water splitting. Prepared from a bubble-templated electrodeposition method and subsequent low-temperature phosphidization, NiCuP has a hierarchical pore structure with a large electrochemical active surface area. To reach a high current density of 50 mA cm−2, it requires merely 146 and 300 mV with small Tafel slopes of 47 and 49 mV dec−1 for HER and OER, respectively. The total water splitting test using NiCuP as both the anode and cathode showed nearly 100% Faradic efficiency and surpassed the performances of electrode pairs using commercial Pt/C and IrO2 catalysts under our test conditions. The high activity of NiCuP can be attributed to (1) the conductive NiCu substrates, (2) a large electrochemically active surface area together with a combination of pores of different sizes, and (3) the formation of active Ni/Cu oxides/hydroxides while keeping a portion of more conductive Ni/Cu phosphides in the nano-foam. We expect the current catalyst to enable the manufacturing of affordable water splitting systems.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)4401-4408
Sayfa sayısı8
DergiNanoscale
Hacim9
Basın numarası13
DOI'lar
Yayın durumuYayınlandı - 7 Nis 2017
Harici olarak yayınlandıEvet

Bibliyografik not

Publisher Copyright:
© The Royal Society of Chemistry.

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