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Single-Step Synthesis of W2C Nanoparticle-Dispersed Carbon Electrocatalysts for Hydrogen Evolution Reactions Utilizing Phosphate Groups on Carbon Edge Sites
Author(s) -
Takafumi Ishii,
Keita Yamada,
Noriko Osuga,
Yasuo Imashiro,
Junichi Ozaki
Publication year - 2016
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.6b00179
Subject(s) - tafel equation , calcination , nanoparticle , catalysis , materials science , carbon fibers , tungsten , tungsten carbide , chemical engineering , inorganic chemistry , carbon nanotube , carbide , substrate (aquarium) , hydrogen , nanotechnology , chemistry , organic chemistry , metallurgy , composite material , electrochemistry , composite number , oceanography , electrode , geology , engineering
A novel, one-step protocol for the selective synthesis of W 2 C nanoparticles from phosphotungstic acid (H 3 PW 12 O 40 ), a low-cost and commercially available tungsten compound, was developed. The nanoparticles had diameters of 1-50 nm and were dispersed on a carbon substrate. The W 2 C nanoparticles were prepared by a simple operation sequence, involving impregnation of carbon black with H 3 PW 12 O 40 followed by calcination at 1000 °C. X-ray diffraction study revealed the selective formation of the W 2 C phase in the samples prepared, whereas the tungsten carbide (WC) phase was present in the control prepared from H 2 WO 4 . Stable W 2 C nanoparticles were obtained using this method owing to the presence of phosphate at the interfaces between the W 2 C nanoparticles and the carbon substrates, which inhibited the diffusion of carbon atoms from the carbon substrates to the W 2 C nanoparticles, leading to the formation of WC. The W 2 C nanoparticles prepared showed an excellent catalytic activity for the hydrogen evolution reaction (HER), with low Tafel slopes of ∼50 mV/decade. The HER catalytic activity was notably high, being comparable to that of MoS 2 , which is a promising alternative to Pt. The present method can potentially be applied to produce highly effective, low-cost, Pt-free electrocatalysts for the HER.

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