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Synthesize and Characterization of 2‐Aminothiazole Monomer and Polymer‐based Bifunctional Fe/N/C Catalysts for Oxygen and Carbon Dioxide Reduction Reactions
Author(s) -
Zhang Qi,
Jiang Hui,
Niu Dongfang,
Zhang Xinsheng,
Sun Shigang,
Hu Shuozhen
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201900690
Subject(s) - bifunctional , monomer , overpotential , polymerization , catalysis , polymer , chemistry , pyridine , polymer chemistry , copolymer , inorganic chemistry , materials science , organic chemistry , electrochemistry , electrode
2‐aminothiazole monomer (AT‐monomer) and polymer (AT‐polymer) are utilized as the nitrogen source to synthesize the Fe/N/C catalysts. The polymerization effect of nitrogen source for Fe/N/C catalysts on their bifunctional activity toward oxygen reduction reaction (ORR) and CO 2 reduction reaction (CO 2 RR) is investigated. Both AT‐monomer‐Fe/N/C and AT‐polymer‐Fe/N/C contain pyridine N (including Fe−N) and graphitic N in the structure, resulting in displaying bifunctional activity toward ORR and CO 2 RR. The 2‐aminothiazole polymer structure is important to produce graphene structured nanosheets with higher amount of defect sites and more pyridinic N (including Fe−N) and graphitic N in AT‐polymer‐Fe/N/C than those in AT‐monomer‐Fe/N/C synthesized from 2‐aminothiazole monomers. With the structure advantages, AT‐polymer‐Fe/N/C displays superior bifunctional catalytic performance. It has higher catalytic efficiency than commercial Pt/C for ORR and high CO selectivity (92%) with 4.2 mA cm –2 at overpotential of 0.47 V for CO 2 RR than that of AT‐monomer‐Fe/N/C.
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