Nitrogen and oxygen dual-doped porous carbons prepared from pea protein as electrode materials for high performance supercapacitors

DEMİR, MÜSLÜM; Ashourirad, Babak; Mugumya, Jethrine; Saraswat, Sushil; El-Kaderi, Hani; Gupta, Ram

doi:10.1016/j.ijhydene.2018.03.220

Nitrogen and oxygen dual-doped porous carbons prepared from pea protein as electrode materials for high performance supercapacitors

DEMİR M., Ashourirad B., Mugumya J. H., Saraswat S. K., El-Kaderi H. M., Gupta R. B.

International Journal of Hydrogen Energy, cilt.43, sa.40, ss.18549-18558, 2018 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 43 Sayı: 40
Basım Tarihi: 2018
Doi Numarası: 10.1016/j.ijhydene.2018.03.220
Dergi Adı: International Journal of Hydrogen Energy
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.18549-18558
Anahtar Kelimeler: Biochar, Electrode, Nitrogen and oxygen co-doping, Porous carbons, Supercapacitor
Boğaziçi Üniversitesi Adresli: Hayır

Özet

Porous carbons as electrode materials are highly desired for use in energy storage/conversion devices. Herein, the development of a series of highly porous nitrogen and oxygen co-doped carbons by using pea protein (PP) as a cost-effective, sustainable and nitrogen-rich precursor is reported. Pea protein derived carbons (PPDCs) have been prepared by applying a straightforward two-step synthetic route including pyrolysis and KOH-chemical activation. Potassium hydroxide has been employed to generate porosity and introduce oxygen functionalities into the framework of carbon. The heteroatoms doping content and porosity parameters have been tuned by varying the synthesis temperature and activator to precursor ratio. The carbon obtained with optimal synthetic parameters (T = 800 °C and KOH/Precursor = 4) featured the highest surface area, the maximal pore volume and N-/O doping level of 3500 m2 g−1, 1.76 cm3 g−1, and 2.5-/17.9 at%, respectively. PPDC-4-800 as supercapacitor presented a very high specific capacitance (413 F g−1 at 1.0 A g−1 in 1 M KOH), remarkable cycling stability (92% retention after 20000 cycles) and outstanding rate capability (210 F g−1 at 30 A g−1). The cooperative effects of the well-developed porous architecture and surface modification of PPDCs resulted in enhanced electrochemical performances, suggesting their potential application for energy storage devices.