Biowaste-derived 3D honeycomb-like N and S dual-doped hierarchically porous carbons for high-efficient CO2 capture

33Citations
Citations of this article
38Readers
Mendeley users who have this article in their library.

Abstract

Considering the characteristics of abundant narrow micropores of <1 nm, appropriate proportion of mesopores/macropores and suitable surface functionalization for a highly-efficient carbon-based CO2 adsorbent, we proposed a facile and cost-effective strategy to prepare N and S dual-doped carbons with well-interconnected hierarchical pores. Benefiting from the unique structural features, the resultant optimal material showed a prominent CO2 uptake of up to 7.76 and 5.19 mmol g-1 at 273 and 298 K under 1 bar, and importantly, a superb CO2 uptake of 1.51 mmol g-1 at 298 K and 0.15 bar was achieved, which was greatly significant for CO2 capture from the post-combustion flue gases in practical application. A systematic study demonstrated that the synergetic effect of ultramicroporosity and surface functionalization determined the CO2 capture properties of porous carbons, and the synergistic influence mechanism of nitrogen/sulfur dual-doping on CO2 capture performance was also investigated in detail. Importantly, such as-prepared carbon-based CO2 adsorbents also showed an outstanding recyclability and CO2/N2 selectivity. In view of cost-effective fabrication, the excellent adsorption capacity, high selectivity and simple regeneration, our developed strategy was valid and convenient to design a novel and highly-efficient carbonaceous adsorbent for large-scale CO2 capture and separation from post-combustion flue gases.

Cite

CITATION STYLE

APA

Shi, W., Wang, R., Liu, H., Chang, B., Yang, B., & Zhang, Z. (2019). Biowaste-derived 3D honeycomb-like N and S dual-doped hierarchically porous carbons for high-efficient CO2 capture. RSC Advances, 9(40), 23241–23253. https://doi.org/10.1039/c9ra03659h

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free