TY - JOUR
T1 - Photocatalytic performance of dual-function selenium-enriched biomass-derived activated carbon as a catalyst for dye degradation and hydrogen production
AU - Kanwal, Hajirah
AU - Khoja, Asif Hussain
AU - Hajji, Yassine
AU - Shakir, Sehar
AU - Anwar, Mustafa
AU - Liaquat, Rabia
AU - Din, Israf Ud
AU - Bahadar, Ali
AU - Hleili, Manel
N1 - Publisher Copyright:
© 2024 Hydrogen Energy Publications LLC
PY - 2025/2/3
Y1 - 2025/2/3
N2 - In this work, hemp-derived biochar (BC) was synthesized and then activated with KOH to achieve activated carbon (AC). The selenium (Se 1, 3, 5 wt%) was loaded over AC and characterized using various techniques to investigate the physicochemical, electrochemical, and photocatalytic performance for dye degradation and H2 generation as dual function photocatalyst. BC, AC, and the influence of different loading of Se (1 wt%, 3 wt%, 5 wt%) were examined for the degradation of crystal violet (CV) dye under sunlight. Amongst 3% Se-AC showed the maximum degradation efficiency (98.2%) of CV dye within 75 min and the electrons (e−) had a major contribution to the degradation of CV during the active radical trap test. The photocatalytic H2 production performance was tested and the maximum H2 rate 3095 μmol/g/h and light to hydrogen efficiency (LTH) 2.36% were achieved for 3% Se-AC. The post-reaction characterization showed competitive stability. A possible reaction mechanism was proposed for photocatalytic H2 production and it is suggested that the Se loading played a key role in charge transfer enhancement due to high polarizability, d-electron richness, and its bond energy with hydrogen atoms (Se-Hads is 273 kJ/mol) is comparable to the platinum (Pt) (Pt-Hads is 251 kJ/mol).
AB - In this work, hemp-derived biochar (BC) was synthesized and then activated with KOH to achieve activated carbon (AC). The selenium (Se 1, 3, 5 wt%) was loaded over AC and characterized using various techniques to investigate the physicochemical, electrochemical, and photocatalytic performance for dye degradation and H2 generation as dual function photocatalyst. BC, AC, and the influence of different loading of Se (1 wt%, 3 wt%, 5 wt%) were examined for the degradation of crystal violet (CV) dye under sunlight. Amongst 3% Se-AC showed the maximum degradation efficiency (98.2%) of CV dye within 75 min and the electrons (e−) had a major contribution to the degradation of CV during the active radical trap test. The photocatalytic H2 production performance was tested and the maximum H2 rate 3095 μmol/g/h and light to hydrogen efficiency (LTH) 2.36% were achieved for 3% Se-AC. The post-reaction characterization showed competitive stability. A possible reaction mechanism was proposed for photocatalytic H2 production and it is suggested that the Se loading played a key role in charge transfer enhancement due to high polarizability, d-electron richness, and its bond energy with hydrogen atoms (Se-Hads is 273 kJ/mol) is comparable to the platinum (Pt) (Pt-Hads is 251 kJ/mol).
KW - Dual function catalyst
KW - Dye degradation
KW - Photocatalytic hydrogen production
KW - Se-loaded activated carbon
UR - http://www.scopus.com/inward/record.url?scp=85214097959&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2024.12.509
DO - 10.1016/j.ijhydene.2024.12.509
M3 - Article
AN - SCOPUS:85214097959
SN - 0360-3199
VL - 101
SP - 1288
EP - 1303
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -