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Nanocasting SiO(2) into metal–organic frameworks imparts dual protection to high-loading Fe single-atom electrocatalysts

Single-atom catalysts (SACs) have sparked broad interest recently while the low metal loading poses a big challenge for further applications. Herein, a dual protection strategy has been developed to give high-content SACs by nanocasting SiO(2) into porphyrinic metal–organic frameworks (MOFs). The py...

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Detalles Bibliográficos
Autores principales: Jiao, Long, Zhang, Rui, Wan, Gang, Yang, Weijie, Wan, Xin, Zhou, Hua, Shui, Jianglan, Yu, Shu-Hong, Jiang, Hai-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275045/
https://www.ncbi.nlm.nih.gov/pubmed/32504040
http://dx.doi.org/10.1038/s41467-020-16715-6
Descripción
Sumario:Single-atom catalysts (SACs) have sparked broad interest recently while the low metal loading poses a big challenge for further applications. Herein, a dual protection strategy has been developed to give high-content SACs by nanocasting SiO(2) into porphyrinic metal–organic frameworks (MOFs). The pyrolysis of SiO(2)@MOF composite affords single-atom Fe implanted N-doped porous carbon (Fe(SA)–N–C) with high Fe loading (3.46 wt%). The spatial isolation of Fe atoms centered in porphyrin linkers of MOF sets the first protective barrier to inhibit the Fe agglomeration during pyrolysis. The SiO(2) in MOF provides additional protection by creating thermally stable FeN(4)/SiO(2) interfaces. Thanks to the high-density Fe(SA) sites, Fe(SA)–N–C demonstrates excellent oxygen reduction performance in both alkaline and acidic medias. Meanwhile, Fe(SA)–N–C also exhibits encouraging performance in proton exchange membrane fuel cell, demonstrating great potential for practical application. More far-reaching, this work grants a general synthetic methodology toward high-content SACs (such as Fe(SA), Co(SA), Ni(SA)).