Abstract:The use of magnetic nanoparticles to convert electromagnetic energy into heat is known to be a key strategy for numerous biomedical applications but is also an approach of growing interest in the field of catalysis. The heating efficiency of magnetic nanoparticles is limited by the poor magnetic properties of most of them. Here we show that the new generation of iron carbide nanoparticles of controlled size and with over 80 % crystalline Fe C leads to exceptional heating properties, which are much better than … Show more
“…Transition metals (e. g., Fe, Mn, Ni) were previously reported to possess high selectivity for producing CO as electrocatalysts of CO 2 RR . Recent researches have shown that the Fe/Fe 3 C is a promising precious metal free catalyst for a series of important reactions, including CO 2 hydrogenation catalysts, and ammonia decomposition processes, inspiring us to study the electrocatalytic properties of Fe/Fe 3 C toward CO 2 RR.…”
Hybrids of Fe/Fe3C embedded in N‐doped carbon nanotubes (Fe/Fe3C@NCNTs) are prepared by pyrolyzing mixtures of Fe3O4 nanoparticles and dicyandiamide. The systematic electrochemical study of Fe/Fe3C@NCNTs shows a decent catalytic activity toward the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR). The sample of Fe/Fe3C@NCNTs at 750 °C exhibits a remarkably high activity with an onset potential of 1.47 V for the OER, and an onset potential of 0.96 V and half‐wave potential 0.88 V for the ORR, which inspired us to set up a rechargeable Zn‐air battery with such Fe/Fe3C@NCNT nanohybrids as the cathode materials, showing a maximum power density of 198 mW cm−2 and long‐term stability after 500 cycles. We also demonstrate that Fe/Fe3C@NCNTs present favorable electrocatalytic activity towards the CO2 reduction reaction (CO2RR) with a low onset potential and good selectivity. The major products are a mixture of H2 and CO gases that can be used for methanol production in the Fischer−Tropsch process.
“…Transition metals (e. g., Fe, Mn, Ni) were previously reported to possess high selectivity for producing CO as electrocatalysts of CO 2 RR . Recent researches have shown that the Fe/Fe 3 C is a promising precious metal free catalyst for a series of important reactions, including CO 2 hydrogenation catalysts, and ammonia decomposition processes, inspiring us to study the electrocatalytic properties of Fe/Fe 3 C toward CO 2 RR.…”
Hybrids of Fe/Fe3C embedded in N‐doped carbon nanotubes (Fe/Fe3C@NCNTs) are prepared by pyrolyzing mixtures of Fe3O4 nanoparticles and dicyandiamide. The systematic electrochemical study of Fe/Fe3C@NCNTs shows a decent catalytic activity toward the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR). The sample of Fe/Fe3C@NCNTs at 750 °C exhibits a remarkably high activity with an onset potential of 1.47 V for the OER, and an onset potential of 0.96 V and half‐wave potential 0.88 V for the ORR, which inspired us to set up a rechargeable Zn‐air battery with such Fe/Fe3C@NCNT nanohybrids as the cathode materials, showing a maximum power density of 198 mW cm−2 and long‐term stability after 500 cycles. We also demonstrate that Fe/Fe3C@NCNTs present favorable electrocatalytic activity towards the CO2 reduction reaction (CO2RR) with a low onset potential and good selectivity. The major products are a mixture of H2 and CO gases that can be used for methanol production in the Fischer−Tropsch process.
“…The spatial separation of the heating agent and the catalyst, by depositing Fe 2.2 C NPs on an inorganic support previously impregnated Ru or Ni NPs, led to CH 4 yields higher than 90 % at low magnetic field (ca. 20 mT) . Almost simultaneously, Mortensen et al .…”
Section: Figurementioning
confidence: 94%
“…Magnetic induction has recently appeared as an alternative heating source for heterogeneous catalytic reactions . It consists in applying high‐frequency alternating magnetic fields to ferromagnetic materials to release heat through hysteresis losses.…”
Section: Figurementioning
confidence: 99%
“…This technology appeared first as an engineer solution for fast heating catalytic reactors, making use either of the walls of the reactor or from heating elements embedded inside, such as iron balls or ferrite microparticles . We have demonstrated the possibility to magnetically induce CO 2 methanation in a continuous‐flow reactor using core–shell NPs consisting of Ni or Ru coated iron carbide cores displaying high heating properties . However, a modest CO 2 conversion (50 %) was achieved with a CH 4 yield of 15 %.…”
Induction heating of magnetic nanoparticles (NPs) is a method to activate heterogeneous catalytic reactions. It requires nano‐objects displaying high heating power and excellent catalytic activity. Here, using a surface engineering approach, bimetallic NPs are used for magnetically induced CO2 methanation, acting both as heating agent and catalyst. The organometallic synthesis of Fe30Ni70 NPs displaying high heating powers at low magnetic field amplitudes is described. The NPs are active but only slightly selective for CH4 after deposition on SiRAlOx owing to an iron‐rich shell (25 mL min−1, 25 mT, 300 kHz, conversion 71 %, methane selectivity 65 %). Proper surface engineering consisting of depositing a thin Ni layer leads to Fe30Ni70@Ni NPs displaying a very high activity for CO2 hydrogenation and a full selectivity. A quantitative yield in methane is obtained at low magnetic field and mild conditions (25 mL min−1, 19 mT, 300 kHz, conversion 100 %, methane selectivity 100 %).
“…Magnetic nanoparticles (NPs) are objects of choice for a wide range of applications, such as data storage,, catalysis, and biomedical ones ,. Among the different properties sought, the potential overheating of the nanoparticles in presence of an alternate magnetic field received tremendous interest due to its implication on Magnetic Field Hyperthermia (MFH) treatment and thermally‐assisted catalysis ,. To benefit from optimized heating properties, high saturation magnetization (M S ) materials are mandatory ,.…”
A novel approach for the synthesis of Fe(0) nanoparticles (NPs) with tunable sizes and shapes is reported. Ultrasmall Fe(0) NPs were reacted under mild conditions in the presence of a mixture of palmitic acid and amine ligands. These NPs acted not only as preformed seeds but also as an internal iron(II) source that was produced by the partial dissolution of the NPs by the acid. This fairly simple approach allows the strict separation of the nucleation and the growth steps. By changing the acid concentration, a fine tuning of the relative ratio between the remaining Fe(0) seeds and the iron(II) reservoir was achieved, giving access to both size (from 7 to 20 nm) and shape (spheres, cubes or stars) control. The partial dissolution of the ultrasmall Fe(0) NPs into iron(II) source and the successive growth was further studied by using combined TEM and Mössbauer spectroscopy. The successive corrosion, coalescence, and ripening observed could be understood in the framework of an environment‐dependent growth model.
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