TY - JOUR
T1 - Metal phosphide nanoparticles embedded in carbon as efficient electrocatalyst for oxygen evolution reaction
AU - Shanmugam, Sangaraju
AU - Sivanantham, Arumugam
AU - Matsunaga, Mariko
AU - Simon, Ulrich
AU - Osaka, Tetsuya
N1 - Funding Information:
This work was financially supported by the DGIST R&D Program of the Ministry of Science, ICT and Future Planning of Korea ( 18-IT-02 ).
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2019/2/20
Y1 - 2019/2/20
N2 - We describe a facile and simple solid-state thermolysis route for the preparation of Co, Ni, and Fe phosphide nanoparticles embedded in amorphous carbon using an organometallic complex. This was achieved by using a suitable organometallic complex in a single step synthetic route without using any solvent or catalyst. The advantage of using such precursor was to offer a source for metal, phosphorus and carbon without using any additional sources. The morphology of products was characterized by transmission electron microscopy, scanning electron microscopy and nature of carbon was analyzed using the Raman microscope and X-ray diffraction. The electrocatalytic oxygen evolution reaction (OER) activity and stability of the metal phosphide nanostructure was evaluated using the rotating disk electrode technique. The CoP, NiP and FeP exhibit the OER overpotential of 370, 380 and 550 mV at 10 mA cm−2, respectively in 0.1 M KOH electrolyte. Among prepared phosphide catalysts, cobalt phosphide shows a lowest Tafel slope indicate favorable kinetics for the OER activity than nickel and iron phosphide catalysts.
AB - We describe a facile and simple solid-state thermolysis route for the preparation of Co, Ni, and Fe phosphide nanoparticles embedded in amorphous carbon using an organometallic complex. This was achieved by using a suitable organometallic complex in a single step synthetic route without using any solvent or catalyst. The advantage of using such precursor was to offer a source for metal, phosphorus and carbon without using any additional sources. The morphology of products was characterized by transmission electron microscopy, scanning electron microscopy and nature of carbon was analyzed using the Raman microscope and X-ray diffraction. The electrocatalytic oxygen evolution reaction (OER) activity and stability of the metal phosphide nanostructure was evaluated using the rotating disk electrode technique. The CoP, NiP and FeP exhibit the OER overpotential of 370, 380 and 550 mV at 10 mA cm−2, respectively in 0.1 M KOH electrolyte. Among prepared phosphide catalysts, cobalt phosphide shows a lowest Tafel slope indicate favorable kinetics for the OER activity than nickel and iron phosphide catalysts.
KW - Cobalt phosphide
KW - Metal phosphide
KW - Nanoparticles
KW - Oxygen evolution reaction
KW - Water splitting
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U2 - 10.1016/j.electacta.2018.12.028
DO - 10.1016/j.electacta.2018.12.028
M3 - Article
AN - SCOPUS:85059324275
SN - 0013-4686
VL - 297
SP - 749
EP - 754
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -