N, S Co-doped porous carbons from coconut shell for selective CO2 adsorption


Shao J., Wang Y., Che M., Xiao Q., DEMİR M., Al Mesfer M. K., ...Daha Fazla

Journal of the Energy Institute, cilt.123, 2025 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 123
  • Basım Tarihi: 2025
  • Doi Numarası: 10.1016/j.joei.2025.102273
  • Dergi Adı: Journal of the Energy Institute
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Chemical Abstracts Core, Compendex, Environment Index, INSPEC
  • Anahtar Kelimeler: CO 2 adsorption, N/S co-doping, Microporosity, Biomass-derived carbon, Thiourea
  • Boğaziçi Üniversitesi Adresli: Hayır

Özet

The CO2 capture from flue gas using biomass-derived porous carbons offers a promising and sustainable approach to mitigate greenhouse gas emissions. However, achieving high adsorption performance under ambient conditions requires synergistic optimization of pore architecture and surface chemistry. In the present work, a facile and scalable synthesis method was developed to prepare nitrogen and sulfur co-doped porous carbons using coconut shell as a renewable carbon precursor and thiourea as a dual heteroatom source. Chemical activation with KOH was employed to tune the porosity and surface functionality. The optimal adsorbent exhibited a high BET surface area (1315 m2/g), large narrow micropore volume (0.66 cm3/g), and significant heteroatom content (3.39 at.% N and 0.39 at.% S), resulting in superior CO2 uptake of 4.38 and 6.46 mmol/g at 25 °C and 0 °C, 1 bar, respectively. Additionally, as-prepared adsorbents demonstrated high CO2/N2 selectivity, rapid adsorption kinetics, moderate isosteric heat of adsorption, and excellent cycling stability over five adsorption–desorption cycles. These findings underscore the dual role of narrow micropores and heteroatom-rich functional groups in enhancing gas–solid interactions and provide a green and effective strategy for designing high-efficiency CO2 sorbents from coconut shell waste.