Transition metaleincorporated tungsten-based ternary refractory metal selenides (MWSex; M = Fe, Co, Ni, and Mn) as hydrogen evolution catalysts at soft interfaces
| dc.authorid | 0000-0003-1463-9764 | en_US |
| dc.authorid | 0000-0002-3935-9649 | en_US |
| dc.authorid | 0000-0002-3689-0469 | en_US |
| dc.contributor.author | Aslan, E. | |
| dc.contributor.author | Sarılmaz, Adem | |
| dc.contributor.author | Yanalak, G. | |
| dc.contributor.author | Özel, Sultan Süleyman | |
| dc.contributor.author | Özel, Faruk | |
| dc.contributor.author | Patir, I. H. | |
| dc.date.accessioned | 2021-01-19T10:47:12Z | |
| dc.date.available | 2021-01-19T10:47:12Z | |
| dc.date.issued | 2020 | en_US |
| dc.department | KMÜ, Mühendislik Fakültesi, Metalurji ve Malzeme Mühendisliği Bölümü | en_US |
| dc.description | WOS:000601397500007 | en_US |
| dc.description.abstract | Hydrogen evolution reaction (HER) catalysts including transition metal chalcogenides have been recognized as a class of very promising non-expensive and earth-abundant catalysts. Tremendous investigations on the binary and ternary metal sulfides/selenides have demonstrated extraordinary chemical and physical properties such as good structural stability and adjustable chemical composition. The ternary amorphous refractory metal selenides (MWSex; M = Fe, Co, Ni, Mn) have been synthesized by the hot-injection method. The NiWSex, CoWSex, FeWSex and MnWSex nanostructures have been used as catalysts for the hydrogen evolution at the biphasic systems of water and 1,2-dichloroethane with similar to a biomembrane. The catalytic activity differences of ternary metal selenides have been compared with each other taking into account transition metals which are changed in the order of Fe approximate to Mn << Co < Ni. The catalytic activities of the MWSex have not been changed when adding of Fe and Mn into the tungsten selenide nanostructure, which may be originated from amorphous structures of FeWSex and MnWSex. Ni and Co addition into the tungsten selenide have improved the electrocatalytic HER activity when compared with only WSex. | en_US |
| dc.description.sponsorship | The authors would like to thank TUBITAK (The Scientific and Technological Research Council of Turkey) (Grant number: 215M309) and Turkish Academy of Sciences via a TUBA-GEBIP fellowship for supporting this work. | en_US |
| dc.identifier.citation | Aslan, E., Sarılmaz, A., Yanalak, G.,Özel, S. S., Ozel, F.,Patir, I. H.(2020).Transition metaleincorporated tungsten-based ternary refractory metal selenides (MWSex; M = Fe, Co, Ni, and Mn) as hydrogen evolution catalysts at soft interfaces.Materials Today Energy, 18. | en_US |
| dc.identifier.doi | 10.1016/j.mtener.2020.100510 | |
| dc.identifier.issn | 2468-6069 | |
| dc.identifier.scopus | 2-s2.0-85091261913 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1016/j.mtener.2020.100510 | |
| dc.identifier.uri | https://hdl.handle.net/11492/4761 | |
| dc.identifier.volume | 18 | en_US |
| dc.identifier.wos | WOS:000601397500007 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Sceince | |
| dc.indekslendigikaynak | Scopus | |
| dc.institutionauthor | Sarılmaz, Adem | |
| dc.institutionauthor | Özel, Sultan Süleyman | |
| dc.institutionauthor | Özel, Faruk | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | en_US |
| dc.relation.journal | Materials Today Energy | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.relation.tubitak | 215M309 | |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Ternary Metal Selenides | en_US |
| dc.subject | Hydrogen Evolution Reaction | en_US |
| dc.subject | Liquid/Liquid İnterfaces | en_US |
| dc.subject | Iron Tungsten Selenide | en_US |
| dc.subject | Manganese Tungsten Selenide | en_US |
| dc.title | Transition metaleincorporated tungsten-based ternary refractory metal selenides (MWSex; M = Fe, Co, Ni, and Mn) as hydrogen evolution catalysts at soft interfaces | en_US |
| dc.type | Article |












