TY - JOUR
T1 - Electronic state tuning over Mo-doped W18O49 ultrathin nanowires with enhanced molecular oxygen activation for desulfurization
AU - Xiong, Jun
AU - Li, Jiayu
AU - Huang, Haoxue
AU - Zhang, Ming
AU - Zhu, Wenshuai
AU - Zhou, Jiadong
AU - Li, Huaming
AU - Di, Jun
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Developing catalyst with abundant surface active sites is the core issue to achieve efficient catalytic oxidative desulfurization performance. In this work, Mo doped W18O49 ultrathin nanowires is fabricated through solvothermal method to provide plentiful low coordinated metal atoms around oxygen vacancies to trigger oxidative desulfurization reaction. As a non-stoichiometric oxide, the discorded lattice microstructure in W18O49 endows the formation of O vacancies neighboring low-valence W atoms, while the ultrathin structure ensure the fully exposure of surface atoms. Moreover, the doped Mo atoms will tune the surface atomic structure and electronic state of W18O49 nanowires, leading to the higher oxygen vacancy concentration and strengthened interaction with target sulfide molecules. Benefiting from these features, the higher molecular oxygen activation capacity can be realized over Mo-W18O49 nanowires to yield more superoxide radicals, making it with greatly improved oxidative desulfurization performance. The optimized 2 %Mo-W18O49 catalyst shows nearly 100% removal of dibenzothiophene within 5 h and maintain the good cycle stability. This work supply new insights for the design of catalytic sites towards selective catalytic oxidative desulfurization.
AB - Developing catalyst with abundant surface active sites is the core issue to achieve efficient catalytic oxidative desulfurization performance. In this work, Mo doped W18O49 ultrathin nanowires is fabricated through solvothermal method to provide plentiful low coordinated metal atoms around oxygen vacancies to trigger oxidative desulfurization reaction. As a non-stoichiometric oxide, the discorded lattice microstructure in W18O49 endows the formation of O vacancies neighboring low-valence W atoms, while the ultrathin structure ensure the fully exposure of surface atoms. Moreover, the doped Mo atoms will tune the surface atomic structure and electronic state of W18O49 nanowires, leading to the higher oxygen vacancy concentration and strengthened interaction with target sulfide molecules. Benefiting from these features, the higher molecular oxygen activation capacity can be realized over Mo-W18O49 nanowires to yield more superoxide radicals, making it with greatly improved oxidative desulfurization performance. The optimized 2 %Mo-W18O49 catalyst shows nearly 100% removal of dibenzothiophene within 5 h and maintain the good cycle stability. This work supply new insights for the design of catalytic sites towards selective catalytic oxidative desulfurization.
KW - Catalytic oxidative desulfurization
KW - Electronic state tuning
KW - Mo-WO
KW - Molecular oxygen activation
UR - http://www.scopus.com/inward/record.url?scp=85129702637&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2022.121167
DO - 10.1016/j.seppur.2022.121167
M3 - Article
AN - SCOPUS:85129702637
SN - 1383-5866
VL - 294
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 121167
ER -