Tin sulfide supported on cellulose nanocrystals-derived carbon as a green and effective catalyst for CO2 electroreduction to formate
This work reports a whole green two-step approach for the synthesis of novel catalysts for efficient CO 2 conversion. A conductive carbon support was firstly obtained via pyrolysis of cellulose nanocrystals (CNCs), and the carbon surface was successively decorated with tin sulfide (SnS) through a mi...
Gespeichert in:
Veröffentlicht in: | Journal of materials science 2023-10, Vol.58 (37), p.14673-14685 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This work reports a whole green two-step approach for the synthesis of novel catalysts for efficient CO
2
conversion. A conductive carbon support was firstly obtained via pyrolysis of cellulose nanocrystals (CNCs), and the carbon surface was successively decorated with tin sulfide (SnS) through a microwave-assisted hydrothermal process. The morphology and carbon structure were characterized by field emission scanning electron microscopy and Raman spectroscopy, and the presence of SnS decoration was confirmed by X-ray photoelectron spectroscopy and X-ray diffraction analyses. The SnS supported on CNC-derived carbon shows enhanced catalytic activity for the CO
2
conversion to formate (HCOO
−
). Good selectivity of 86% and high partial current density of 55 mA cm
−2
are reached at − 1.0 V vs. reversible hydrogen electrode in KHCO
3
electrolyte. Additionally, the mass activity of the composite catalyst achieves a value as high as 262.9 mA mg
Sn
−1
for HCOO
−
formation, demonstrating good utilization efficiency of Sn metal. In this work, the low-cost CNC-derived carbon is evidenced to be easily decorated with metal species and thus shows high versatility and tailorability. Incorporating metal species with conductive high-surface carbon supports represents an effective strategy to realize active and stable electrocatalysts, allowing efficient utilization of metals especially the raw and precious ones.
Graphical abstract |
---|---|
ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-023-08925-2 |