Mesoporous Single-Atom-Doped Graphene-Carbon Nanotube Hybrid: Synthesis and Tunable Electrocatalytic Activity for Oxygen Evolution and Reduction Reactions

Mohammad Tavakkoli*, Emmanuel Flahaut, Pekka Peljo, Jani Sainio, Fatemeh Davodi, Egor V. Lobiak, Kimmo Mustonen, Esko I. Kauppinen

*Tämän työn vastaava kirjoittaja

Tutkimustuotos: LehtiartikkeliArticleScientificvertaisarvioitu

26 Sitaatiot (Scopus)
58 Lataukset (Pure)

Abstrakti

Mesoporous heteroatom-doped carbon-based nanomaterials are very promising as catalysts for electrochemical energy conversion and storage. We have developed a one-step catalytic chemical vapor deposition method to grow a highly graphitized graphene nanoflake (GF)-carbon nanotube (CNT) hybrid material doped simultaneously with single atoms of N, Co, and Mo (N-Co-Mo-GF/CNT). This high-surface-area material has a mesoporous structure, which facilitates oxygen mass transfer within the catalyst film, and exhibits a high electrocatalytic activity and stability in oxygen reduction and evolution reactions (ORR and OER) in alkaline media. We have shown that in this metal (M)-N-C catalyst, M (Co, Mo)-C centers are the main sites responsible for OER, while, for ORR, both M and N-C centers synergistically serve as the active sites. We systematically investigated tuning of the ORR and OER activity of the porous catalyst depending on the choice of the underlying substrate. The ORR kinetic current and OER activity for N-Co-Mo-GF/CNT were significantly enhanced when the catalyst was deposited onto a Ni substrate, resulting in an advanced electrocatalytic performance compared to the best bifunctional ORR/OER catalysts reported so far. Using a developed scanning electrochemical microscopy analysis method, we demonstrated that the higher OER reactivity on Ni was attributable to the formation of underlying catalyst/Ni interfacial sites, which are accessible due to the porous, electrolyte-permeable structure of the catalyst.

AlkuperäiskieliEnglanti
Sivut4647-4658
Sivumäärä12
JulkaisuACS Catalysis
Vuosikerta10
Numero8
Varhainen verkossa julkaisun päivämäärä1 tammikuuta 2020
DOI - pysyväislinkit
TilaJulkaistu - 17 huhtikuuta 2020
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

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