Irfan Muhammad, Afzal Saba, Hussain Muzammil, Naz Muhammad Yasin, Shukrullah Shazia, Rahman Saifur, Faraj Mursal Salim Nasar, Ghanim Abdulnour Ali Jazem
Electrical Engineering Department, College of Engineering, Najran University, Najran 61441, Saudi Arabia.
Department of Physics, University of Agriculture, Faisalabad 38040, Pakistan.
ACS Omega. 2023 May 10;8(21):18891-18900. doi: 10.1021/acsomega.3c01262. eCollection 2023 May 30.
Nonthermal plasma is a well-recognized environmentally advantageous method for producing green fuels. This work used different photocatalysts, including PZO, SZO, and SZC for hydrogen production using an atmospheric argon coaxial dielectric barrier discharge (DBD)-based light source. The photocatalysts were produced using a sol-gel route. The DBD discharge column was filled with water, methanol, and the catalyst to run the reaction under argon plasma. The DBD reactor was operated with a 10 kV AC source to sustain plasma for water splitting. The light absorption study of the tested catalysts revealed a decrease in the band gap with an increase in the concentration of Sr and carbon nanotubes (CNTs) in the Sr/ZnO/CNTs series. The photocatalyst SZC demonstrated the lowest photoluminescence (PL) intensity, implying the most quenched recombination of charge carriers. The highest H evolution rate of 2760 μmol h g was possible with the SZC catalyst, and the lowest evolution rate of 56 μmol h g was observed with the PZO catalyst. The photocatalytic activity of SZC was initially high, which decreased slightly over time due to the deactivation of the photocatalyst. The photocatalytic activity decreased from 2760 to 1670 μmol h g at the end of the process.
非热等离子体是一种公认的生产绿色燃料的环境友好型方法。这项工作使用了不同的光催化剂,包括PZO、SZO和SZC,利用基于大气氩同轴介质阻挡放电(DBD)的光源进行制氢。光催化剂采用溶胶-凝胶法制备。DBD放电柱中填充水、甲醇和催化剂,以在氩等离子体下进行反应。DBD反应器由10 kV交流电源运行,以维持用于水分解的等离子体。对测试催化剂的光吸收研究表明,在Sr/ZnO/CNT系列中,随着Sr和碳纳米管(CNT)浓度的增加,带隙减小。光催化剂SZC表现出最低的光致发光(PL)强度,这意味着电荷载流子的复合被最大程度地猝灭。使用SZC催化剂时,最高析氢速率可达2760 μmol h g,而使用PZO催化剂时,观察到的最低析氢速率为56 μmol h g。SZC的光催化活性最初较高,但由于光催化剂失活,随着时间的推移略有下降。在该过程结束时,光催化活性从2760降至1670 μmol h g。