4.7 Article

A co-coordination strategy to realize janus-type bimetallic phosphide as highly efficient and durable bifunctional catalyst for water splitting

Journal

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
Volume 74, Issue -, Pages 11-20

Publisher

JOURNAL MATER SCI TECHNOL
DOI: 10.1016/j.jmst.2020.10.009

Keywords

Bimetallic phosphide; Bifunctional catalyst; Overall water splitting; DFT calculation

Funding

  1. National Natural Science Foundation of China [21773024]
  2. Sichuan Science and Technology Program [20YYJC3786]
  3. Reformation and Development Funds for Local Region Universities from China Government [ZCKJ 2020-11]
  4. Natural Science Foundation of the Tibet Autonomous Region [2016ZR-TU-10]

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A Janus-type dual-ligand metal-organic frameworks derived bimetallic FeCoP nanoparticles embedded carbon nanotube skeleton was synthesized, showing enhanced OER and HER performances with low Tafel slope and good stability in 1M KOH. This material requires only a low voltage to achieve high current density with nearly 100% faradaic efficiency, approaching the performance of Pt and RuO2.
In this work, a Janus-type dual-ligand metal-organic frameworks derived bimetallic (Fe, Co)P nanoparticles embedded carbon nanotube (CNT) skeleton (DLD-FeCoP@CNT) is presented and synthesized via a facile co-coordination synthesis strategy. The DLD-FeCoP@CNT hybrid shows much better performances for OER and HER with much lower Tafel slope of 39.6 (57.1) mV dec(-1), an overpotential of 286 (166) mV @ 10 mA cm(-2) and better stability for OER (HER) in 1 M KOH. Being both cathode and anode for water splitting, it requires only a low voltage of 1.67 V to obtain 10 mA cm(-2) with nearly 100% faradaic efficiency, which is close to Pt/C//RuO2 cell. Density functional theory calculations based on the bimetallic phosphide (Fe0.3Co0.7P) model reveal that, compared with the monometallic FeP or CoP, the enhanced catalytic activities of Fe0.3Co0.7P is mainly manifested in its free energy of H adsorption (Delta G(H*)) closer to zero, larger binding strength for H2O and higher electrical conductivity. (C) 2021 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

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