Photocatalytic performance of dual-function selenium-enriched biomass-derived activated carbon as a catalyst for dye degradation and hydrogen production

被引:0
|
作者
Kanwal, Hajirah [1 ]
Khoja, Asif Hussain [1 ,2 ]
Hajji, Yassine [3 ]
Shakir, Sehar [1 ]
Anwar, Mustafa [1 ]
Liaquat, Rabia [1 ]
Din, Israf Ud [4 ]
Bahadar, Ali [5 ]
Hleili, Manel [6 ]
机构
[1] Natl Univ Sci & Technol NUST, US Pakistan Ctr Adv Studies Energy USPCAS E, Sect H 12, Islamabad 44000, Pakistan
[2] Univ Cincinnati, Dept Chem & Environm Engn ChEE, Cincinnati, OH 45221 USA
[3] Univ Tunis El Manar, Fac Sci Tunis, LR01ES07 Lab Energet & Thermal & Mass Transfer LET, Tunis 1060, Tunisia
[4] Prince Sattam bin Abdulaziz Univ, Coll Sci & Humanities, Chem Dept, POB 173, Alkharj 11942, Saudi Arabia
[5] King Abdulaziz Univ, Dept Chem & Mat Engn, Rabigh 21911, Saudi Arabia
[6] Univ Tabuk, Fac Sci Tabuk, Dept Math, Tabuk 47512, Saudi Arabia
关键词
Dual function catalyst; Se-loaded activated carbon; Dye degradation; Photocatalytic hydrogen production; H-2; PRODUCTION; TIO2; FABRICATION; NANOSHEETS; COMPOSITE; EVOLUTION;
D O I
10.1016/j.ijhydene.2024.12.509
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 mu mol/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).
引用
收藏
页码:1288 / 1303
页数:16
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