2017
DOI: 10.1039/c7ta07729g
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Amorphous MoSx developed on Co(OH)2 nanosheets generating efficient oxygen evolution catalysts

Abstract: aMoSx/Co(OH)2 nanosheets were synthesized by forming amorphous MoSx on Co(OH)2 nanosheets. The aMoSx/Co(OH)2 nanosheets demonstrate excellent OER catalytic activity with only 350 mV at 10 mA cm−2. The incorporation of amorphous molybdenum sulfide enhances the hydrophilicity, favoring the availability of reactant, and induces electron transfer for enhancing the OER catalytic activity of Co(OH)2.

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Cited by 78 publications
(45 citation statements)
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“…We also note that the Co 2p 3/2 XPS spectra of NF@Co 0.75 V 0.25 ‐HNNs has a higher characteristic satellite at 786.7 eV than that of NF@Co‐HNNs, indicating the dominant Co 2+ existing in the NF@Co 0.75 V 0.25 ‐HNNs, because the incorporation of V 3+ takes the partial position of Co 3+ . Further, all the peaks for Co 2p in NF@Co 0.75 V 0.25 ‐HNNs shift toward lower BEs compared with those in NF@Co‐HNNs, indicating an increase of electronic density in NF@Co‐HNNs after the incorporation of V . The O 1s spectra of NF@Co‐HNNs are fitted to three dominant oxygen species, including CO 3 2− , OH − , and Co−O, depending on the post‐processing conditions, while an extra peak assigned to V−O is observed in the O 1s spectra of NF@Co 0.75 V 0.25 ‐HNNs (Figure f).…”
Section: Resultsmentioning
confidence: 91%
“…We also note that the Co 2p 3/2 XPS spectra of NF@Co 0.75 V 0.25 ‐HNNs has a higher characteristic satellite at 786.7 eV than that of NF@Co‐HNNs, indicating the dominant Co 2+ existing in the NF@Co 0.75 V 0.25 ‐HNNs, because the incorporation of V 3+ takes the partial position of Co 3+ . Further, all the peaks for Co 2p in NF@Co 0.75 V 0.25 ‐HNNs shift toward lower BEs compared with those in NF@Co‐HNNs, indicating an increase of electronic density in NF@Co‐HNNs after the incorporation of V . The O 1s spectra of NF@Co‐HNNs are fitted to three dominant oxygen species, including CO 3 2− , OH − , and Co−O, depending on the post‐processing conditions, while an extra peak assigned to V−O is observed in the O 1s spectra of NF@Co 0.75 V 0.25 ‐HNNs (Figure f).…”
Section: Resultsmentioning
confidence: 91%
“…In amorphous monometallic Co [19,117] and Mo [118] sulfides, the OER performance is primarily driven by the metal-sulfur dangling bonds. The presence of SO 4 2À ions also helps to boost the material's hydrophilicity, allowing better electrolyte-electrocatalyst contact to greatly facilitate OER reactions.…”
Section: Monometallic Sulfidesmentioning
confidence: 99%
“…Therefore, water splitting with zero carbon emission is regarded as an environmentally friendly option to generate oxygen and hydrogen as clean fuels sources to relieve the energy crisis problem . Yet, the oxygen evolution reaction (OER), a bottleneck half‐reaction involved with multistep proton‐coupled electron transfer at the anode, required the large overpotential (η) to overcome the sluggish kinetically and hindered practical utilization of water splitting technology . Efficient catalysts should be designed and synthesized to decrease the overpotential and accelerate the kinetically for the OER.…”
Section: Introductionmentioning
confidence: 99%
“…Over the last few decades, extensive attentions have been paid to earth‐abundant and cost‐efficient (3d) transition metal–based alternatives . Apart from the well‐developed metal oxides and (oxy)hydroxides catalysts, metal selenide, nitride, phosphide, boride, and chalcogenide materials have also attracted large research attention for designing excellent OER electrocatalysts .…”
Section: Introductionmentioning
confidence: 99%