Catalytic Hydrogen Evolution from H[sub.2]S Cracking over Cr[sub.x]ZnS Catalyst in a Cylindrical Single-Layered Dielectric Barrier Discharge Plasma Reactor

• Published in: Materials Vol. 15; no. 21
• Main Authors: Afzal, Saba, Hussain, Humaira, Naz, Muhammad Yasin, Shukrullah, Shazia, Ahmad, Irshad, Irfan, Muhammad, Mursal, Salim Nasar Faraj, Legutko, Stanislaw, Kruszelnicka, Izabela, Ginter-Kramarczyk, Dobrochna
• Format: Journal Article
• Language: English
• Published: MDPI AG 01.10.2022
• Subjects: Ethylenediaminetetraacetic acid; Microwave communications; Plasma physics
• ISSN: 1996-1944; 1996-1944
• DOI: 10.3390/ma15217426

The use of non-thermal plasma technology in producing green fuels is a much-appreciated environmentally friendly approach. In this study, an Al[sub.2]O[sub.3]-supported Cr[sub.x]ZnS semiconductor catalyst was tested for hydrogen evolution from hydrogen sulfide (H[sub.2]S) gas by using a single-layered dielectric barrier discharge (DBD) system. The Al[sub.2]O[sub.3]-supported Cr[sub.x]ZnS catalyst (x = 0.20, 0.25, and 0.30) was produced by using a co-impregnation method and characterized for its structural and photocatalytic characteristics. The discharge column of the DBD system was filled with this catalyst and fed with hydrogen sulfide and argon gas. The DBD plasma was sustained with a fixed AC source of 10 kV where plasma produced species and UV radiations activated the catalyst to break H[sub.2]S molecules under ambient conditions. The catalyst (hexagonal-cubic-sphalerite structure) showed an inverse relationship between the band gap and the dopant concentration. The hydrogen evolution decreased with an increase in dopant concentration in the nanocomposite. The Cr[sub.0.20]ZnS catalyst showed excellent photocatalytic activity under the DBD exposure by delivering 100% conversion efficiency of H[sub.2]S into hydrogen. The conversion decreased to 96% and 90% in case of Cr[sub.0.25]ZnS and Cr[sub.0.30]ZnS, respectively.