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Mesoporous Single Atom-Cluster Fe-N/C Oxygen Evolution Electrocatalysts Synthesized with Bottlebrush Block Copolymer-Templated Rapid Thermal Annealing.
Saha, Dipankar; Yu, Hsin-Jung; Wang, Jiacheng; Chen, Xiaobo; Tang, Chaoyun; Senger, Claire; Pagaduan, James Nicolas; Katsumata, Reika; Carter, Kenneth R; Zhou, Guangwen; Bai, Peng; Wu, Nianqiang; Watkins, James J.
Afiliación
  • Saha D; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Yu HJ; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Wang J; Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Prateek; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Chen X; Department of Materials Science and Engineering, Binghamton University, State University of New York at Binghamton, Binghamton, New York 13850, United States.
  • Tang C; Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Senger C; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Pagaduan JN; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Katsumata R; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Carter KR; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Zhou G; Department of Materials Science and Engineering, Binghamton University, State University of New York at Binghamton, Binghamton, New York 13850, United States.
  • Bai P; Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Wu N; Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
  • Watkins JJ; Conte Center for Polymer Research, Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
ACS Appl Mater Interfaces ; 16(11): 13729-13744, 2024 Mar 20.
Article en En | MEDLINE | ID: mdl-38457643
ABSTRACT
Current electrocatalysts for oxygen evolution reaction (OER) are either expensive (such as IrO2, RuO2) or/and exhibit high overpotential as well as sluggish kinetics. This article reports mesoporous earth-abundant iron (Fe)-nitrogen (N) doped carbon electrocatalysts with iron clusters and closely surrounding Fe-N4 active sites. Unique to this work is that the mechanically stable mesoporous carbon-matrix structure (79 nm in pore size) with well-dispersed nitrogen-coordinated Fe single atom-cluster is synthesized via rapid thermal annealing (RTA) within only minutes using a self-assembled bottlebrush block copolymer (BBCP) melamine-formaldehyde resin composite template. The resulting porous structure and domain size can be tuned with the degree of polymerization of the BBCP backbone, which increases the electrochemically active surface area and improves electron transfer and mass transport for an effective OER process. The optimized electrocatalyst shows a required potential of 1.48 V (versus RHE) to obtain the current density of 10 mA/cm2 in 1 M KOH aqueous electrolyte and a small Tafel slope of 55 mV/decade at a given overpotential of 250 mV, which is significantly lower than recently reported earth-abundant electrocatalysts. Importantly, the Fe single-atom nitrogen coordination environment facilitates the surface reconstruction into a highly active oxyhydroxide under OER conditions, as revealed by X-ray photoelectron spectroscopy and in situ Raman spectroscopy, while the atomic clusters boost the single atoms reactive sites to prevent demetalation during the OER process. Density functional theory (DFT) calculations support that the iron nitrogen environment and reconstructed oxyhydroxides are electrocatalytically active sites as the kinetics barrier is largely reduced. This work has opened a new avenue for simple, rapid synthesis of inexpensive, earth-abundant, tailorable, mechanically stable, mesoporous carbon-coordinated single-atom electrocatalysts that can be used for renewable energy production.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos