热液循环
材料科学
水热合成
结晶度
比表面积
多孔性
化学工程
介孔材料
结晶
插层(化学)
相(物质)
高压灭菌器
吸附
纳米技术
化学
无机化学
催化作用
复合材料
物理化学
冶金
工程类
有机化学
生物化学
作者
Zhiyuan Yu,Tianyi Huang,Shafqat Ullah,Yujun Wang,Guangsheng Luo
标识
DOI:10.1021/acs.iecr.4c01796
摘要
1T-phase MoS2, a versatile two-dimensional transition-metal dichalcogenide, is typically synthesized using a one-pot hydrothermal method. However, inadequate control of the sulfurization, reduction, and crystallization processes in the autoclave leads to multilayer 1T-MoS2 with high crystallinity, a small surface area, and few defects. Considering the aforementioned issues, a two-stage microreactor continuous hydrothermal flow synthesis (CHFS) system coupled with accurate control and rapid processing is used to prepare 1T-MoS2 with abundant voids and a large surface area under 250 °C and 4.0–4.5 MPa. And density functional theory calculations reveal that nitrogenous species, acting as reductants and electron donors, lower the energy of 1T-MoS2 by intercalation and surface adsorption, facilitating its swift synthesis within the presulfurization stage for 10 min and reduction stage for 24 min. The precisely controlled synthesis of porous 1T-MoS2, originating from prenucleation clusters, results in a large surface area of 201.5 m2/g, concentrated mesopores of 2–5 nm, and a pore volume of 0.58 cm3/g. Moreover, a significant transformation from the 1T to the 2H phase is prevented by rapid cooling downstream of the CHFS system.
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