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Carbon Nanotube-Supported MoSe<sub>2</sub> Holey Flake:Mo<sub>2</sub>C Ball Hybrids for Bifunctional pH-Universal Water Splitting

141

Citations

146

References

2019

Year

Abstract

The design of cost-effective and efficient electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is pivotal for the molecular hydrogen (H<sub>2</sub>) production from electrochemical water splitting as a future energy source. Herein, we show that the hybridization between multiple HER- and OER-active components is effective for the design and realization of bifunctional electrocatalysts for universal water splitting, i.e., in both acidic and alkaline media. Our strategy relies on the production and characterization of MoSe<sub>2</sub> holey flake:Mo<sub>2</sub>C ball hybrids supported by single-walled carbon nanotube (SWCNT) electrocatalysts. Flakes of MoSe<sub>2</sub> are produced through hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)-aided liquid phase exfoliation (LPE), which promotes both the exfoliation of the materials and the formation of nanopores in the flakes via chemical etching. The amount of H<sub>2</sub>O<sub>2</sub> in the solvent used for the exfoliation process is optimized to obtain ideal high ratio between edge and basal sites ratio, i.e., high-number of electrocatalytic sites. The hybridization of MoSe<sub>2</sub> flakes with commercial ball-like shaped Mo<sub>2</sub>C crystals facilitates the Volmer reaction, which works in both acidic and alkaline media. In addition, the electrochemical coupling between SWCNTs (as support) and MoSe<sub>2</sub>:Mo<sub>2</sub>C hybrids synergistically enhances both HER- and OER-activity of the native components, reaching high η<sub>10</sub> in acidic and alkaline media (0.049 and 0.089 V for HER in 0.5 M H<sub>2</sub>SO<sub>4</sub> and 1 M KOH, respectively; 0.197 and 0.241 V for OER in 0.5 M H<sub>2</sub>SO<sub>4</sub> and 1 M KOH, respectively). The exploitation of the synergistic effects occurring between multicomponent electrocatalysts, coupled with the production of the electrocatalysts themselves through scalable and cost-effective solution-processed manufacturing techniques, is promising to scale-up the production of H<sub>2</sub> via efficient water splitting for the future energy portfolio.

References

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