掺杂剂
加氢脱氧
纳米片
材料科学
催化作用
二硫化钼
兴奋剂
化学工程
密度泛函理论
胶体
纳米技术
过渡金属
无机化学
氧烷
钼
纳米颗粒
粒子(生态学)
光化学
光谱学
氧化还原
氧化态
吸收光谱法
石墨烯
生物量(生态学)
作者
Steven L. Farrell,Noah Osinski,Ingrid J. Paredes,Amani M. Ebrahim,Haoxian Zheng,Yuchen Zhang,Christopher Oyuela,Lu Ma,Steven N. Ehrlich,Srinivas Rangarajan,Anatoly I. Frenkel,Ayaskanta Sahu
标识
DOI:10.1021/acsami.5c24853
摘要
High Resolution Image Download MS PowerPoint Slide The valorization of biomass into biofuels is a critical process for producing renewable fuels. Hydrodeoxygenation (HDO), particularly over doped molybdenum disulfide (MoS 2 ), a transition metal dichalcogenide (TMD) material, is a common representative catalytic reaction system for converting biomass-derived materials into useful hydrocarbons. However, the location and role of dopants, such as Co, in HDO is not fully understood. The effects of dopant location and oxidation state are often precluded by inhomogeneity in the ensemble properties of nanosheet size and dopant dispersion, as well as difficulty in observing the behavior of atomic site behavior directly. Using a colloidal approach to synthesize cobalt-doped MoS 2 nanosheets with controlled dopant concentration, combined with X-ray absorption spectroscopy (XAS) and density functional theory (DFT) calculations, we determine that basal plane doped Co (25% Co:Mo mole ratio) shows peak catalytic activity in HDO of para- cresol, a model biomass-derived compound, and that basal Co sites are demonstrably more active than edge sites. By observing these doping effects in MoS 2 catalysts for HDO, we can further optimize not only the production of carbon-neutral fuels but also direct the tailoring of doped TMD catalysts toward their intended applications.
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