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Iron phthalocyanine with coordination induced electronic localization to boost oxygen reduction reaction.


ABSTRACT: Iron phthalocyanine (FePc) is a promising non-precious catalyst for the oxygen reduction reaction (ORR). Unfortunately, FePc with plane-symmetric FeN4 site usually exhibits an unsatisfactory ORR activity due to its poor O2 adsorption and activation. Here, we report an axial Fe-O coordination induced electronic localization strategy to improve its O2 adsorption, activation and thus the ORR performance. Theoretical calculations indicate that the Fe-O coordination evokes the electronic localization among the axial direction of O-FeN4 sites to enhance O2 adsorption and activation. To realize this speculation, FePc is coordinated with an oxidized carbon. Synchrotron X-ray absorption and Mössbauer spectra validate Fe-O coordination between FePc and carbon. The obtained catalyst exhibits fast kinetics for O2 adsorption and activation with an ultralow Tafel slope of 27.5?mV?dec-1 and a remarkable half-wave potential of 0.90?V. This work offers a new strategy to regulate catalytic sites for better performance.

SUBMITTER: Chen K 

PROVIDER: S-EPMC7441147 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Iron phthalocyanine with coordination induced electronic localization to boost oxygen reduction reaction.

Chen Kejun K   Liu Kang K   An Pengda P   Li Huangjingwei H   Lin Yiyang Y   Hu Junhua J   Jia Chuankun C   Fu Junwei J   Li Hongmei H   Liu Hui H   Lin Zhang Z   Li Wenzhang W   Li Jiahang J   Lu Ying-Rui YR   Chan Ting-Shan TS   Zhang Ning N   Liu Min M  

Nature communications 20200820 1


Iron phthalocyanine (FePc) is a promising non-precious catalyst for the oxygen reduction reaction (ORR). Unfortunately, FePc with plane-symmetric FeN<sub>4</sub> site usually exhibits an unsatisfactory ORR activity due to its poor O<sub>2</sub> adsorption and activation. Here, we report an axial Fe-O coordination induced electronic localization strategy to improve its O<sub>2</sub> adsorption, activation and thus the ORR performance. Theoretical calculations indicate that the Fe-O coordination e  ...[more]

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