Atomically dispersed Fe/N/C composite was synthesized and its role in controlling the oxygen evolution reaction during Li-O(2) battery charging was studied by use of a tetra(ethylene glycol) dimethyl ether-based electrolyte. Li-O(2) cells using Fe/N/C as the cathode catalyst showed lower overpotentials than α-MnO(2)/carbon catalyst and carbon-only material. Gases evolved during the charge step contained only oxygen for Fe/N/C cathode catalyst, whereas CO(2) was also detected in the case of α-MnO(2)/C or carbon-only material; this CO(2) was presumably generated from electrolyte decomposition. Our results reiterate the catalytic effect in reducing overpotentials, which not only enhances battery efficiency but also improves its lifespan by reducing or eliminating electrolyte decomposition. The structure of the Fe/N/C catalyst was characterized by transmission electron microscopy, scanning transmission electron microscopy, inductively coupled plasma optical emission spectroscopy, and X-ray absorption spectroscopy. Iron was found to be uniformly distributed within the carbon matrix, and on average, Fe was coordinated by 3.3 ± 0.6 and 2.2 ± 0.3 low Z elements (C/N/O) at bond distances of ~1.92 and ~2.09 Å, respectively.
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http://dx.doi.org/10.1021/ja3042993 | DOI Listing |
ChemSusChem
December 2024
Institute for Building Energetics, Thermotechnology and Energy Storage (IGTE), University of Stuttgart, Pfaffenwaldring 31, 70569, Stuttgart, Germany.
Resorcinol-formaldehyde based carbon aerogel (CA) has been tailored to meet the requirements as a Fe-N-C carbon support, aiming to provide sufficient, inexpensive cathode catalysts for high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Therefore, different treatments of the aerogel are explored for optimal pore structure and incorporation of surface functionalities, which are crucial for Fe-N-C synthesis and electrochemical performance. Fe-N-Cs of differently modified aerogel are investigated in phosphoric acid electrolyte.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Institute of Materials Science and Devices, School of Materials Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.
Small Methods
October 2024
Tianmushan Laboratory, Hangzhou, 311115, China.
Carbon-supported nitrogen-coordinated iron single-atom (Fe-N-C) catalysts have been regarded among the most promising platinum-group-metal-free catalysts for oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs). Nevertheless, their limited intrinsic activity and unsatisfactory stability have hindered their practical applications. Here, it is reported that the integration of MoC clusters effectively enhances the ORR activity and stability of Fe-N-C catalysts.
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October 2024
School of Architecture, Civil, Environmental and Energy Engineering, Kyungpook National University, Daegu, 41566, Republic of Korea. Electronic address:
Nanoscale
November 2024
Electrochemical Energy & Sensor Research Laboratory, Amity Institute of Click Chemistry Research & Studies, Amity University, Noida, India.
Installing coordinately unsaturated Fe-N-C structural units on polymer-composite-derived N-doped carbon offers highly active Fe-N sites for the electrochemical oxygen evolution reaction (OER) and reactive oxygen species (ROS) generation in tumor cells. An NHCl-driven high-temperature etching method was employed for the formation of FeSA950NC with coordinately unsaturated single Fe-atoms in an Fe-N(sp)-C structural unit together with N vacancies () and sp defects. The carbonization of Fe-phen@ZIF-8 at 800 °C for 30 min under argon, followed by grinding Fe-ZIF-8@RF-urea with NHCl at 950 °C for 2 hours, resulted in sp carbon defects and sites with coordination unsaturation in Fe-N due to NHCl decomposition to NH and HCl, which produced substantial internal stress for etching the carbon matrix.
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