4.6 Article

A superior dye adsorbent towards the hydrogen evolution reaction combining active sites and phase-engineering of (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 31, Pages 15320-15329

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta02496k

Keywords

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Funding

  1. Ministry of Science and Technology [104-2628-M-007-004-MY3, 104-2221-E-007-048-MY3, 106-2923-E-007-006-MY2, 105-2119-M-009-009, 107-2923-E-007-002-MY3, 107-2112-007-M-007-030-MY3, 107-3017-F-007-002]
  2. National Tsing Hua University [105A0088J4]
  3. National Research Foundation of Korea [2017K2A9A1A06056743]

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Here, we demonstrate the successful synthesis of (1T/2H) MoS2/-MoO3 heterostructured nanoflowers at a low temperature of 200 degrees C by a one-step hydrothermal method. By tuning the reaction time under the influence of thiourea and hydrazine hydrate, we established a complete phase-engineered MoS2 with 1T and 2H phases on the surface of -MoO3. Active sites associated with the phase-engineered (1T/2H) MoS2/-MoO3 hybrid nanoflowers enable them to exhibit dual roles as a superior dye adsorbent and an electrocatalyst towards the hydrogen evolution reaction. The 2H-rich (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers prepared at 16 h achieved a high surface area of 37.97 m(2) g(-1), and 97% of the RhB dye with an initial concentration of 47.9 mg L-1 was removed within 10 min through the adsorption process, which is the highest known removal efficiency reported in the literature. As a hydrogen evolution reaction (HER) electrocatalyst in acidic solution, the 1T-rich (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers prepared at 12 h exhibited a highly efficient catalytic activity by achieving a low overpotential of 232 mV at a current density of 10 mA cm(-2), which is comparable to those of previously reported HER catalysts based on MoS2. Moreover, this sample reached a low Tafel slope of 81 mV dec(-1) and was stable when operated for more than 1000 cycles.

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