4.6 Article

Mo2B2 MBene-supported single-atom catalysts as bifunctional HER/OER and OER/ORR electrocatalysts

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 9, 期 1, 页码 433-441

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta08630d

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资金

  1. National Key Research and Development Program of China [2017YFB0701700]
  2. National Natural Science Foundation of China [51871009]

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This study investigated the catalytic activity of Mo2B2 MBene-supported single-atom catalysts for the oxygen evolution reaction, oxygen reduction reaction, and hydrogen evolution reaction. Transition metal atoms embedded in the structure showed potential as bifunctional electrocatalysts with promising applications.
Searching for highly efficient and cost-effective bifunctional electrocatalysts for the oxygen evolution reaction (OER), oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER), which can be applied to water splitting, fuel cells and metal-air batteries, is critical for developing clean and renewable energies. Yet it remains a great challenge. By means of first-principles calculations, we have studied the OER, ORR and HER catalytic activity of Mo2B2 MBene-supported single-atom catalysts (SACs) by embedding a series of transition metal atoms in the Mo vacancy (TM@Mo2B2, TM = Ti, V, Cr, Mn, Fe, Co, Ni and Cu) as electrocatalysts. All TM@Mo2B2 SACs show excellent metallic conductivity, which would be favorable for the charge transfer in electrocatalytic reactions. Importantly, Ni@Mo2B2 can be used as a HER/OER bifunctional electrocatalyst with a lower vertical bar Delta G(H)vertical bar (-0.09 eV) for the HER under 1/4H coverage and a lower overpotential (eta(OER) = 0.52 V) than that of IrO2 (eta(OER) = 0.56 V) for the OER, while Cu@Mo2B2 can be used as an OER/ORR bifunctional electrocatalyst with a lower overpotential (eta(OER) = 0.31 V) than that of IrO2 (eta(OER) = 0.56 V) and RuO2 (eta(OER) = 0.42 V) for the OER and a lower overpotential of 0.34 V than that of Pt (eta(ORR) = 0.45 V) for the ORR, for both of which the transition metal atoms serve as the active sites. This work could open up an avenue for the development of non-noble-metal-based bifunctional MBene electrocatalysts.

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