塔菲尔方程
过电位
二硫化钼
催化作用
钼
过渡金属
材料科学
化学工程
化学
无机化学
电化学
电极
物理化学
冶金
有机化学
工程类
作者
Tuan Van Nguyen,Thang Phan Nguyen,Quyet Van Le,Dung Van Dao,Sang Hyun Ahn,Soo Young Kim
标识
DOI:10.1016/j.apsusc.2022.154979
摘要
Among various transition metal dichalcogenides, molybdenum disulfides such as molybdenum disulfide nanoflowers (MoS2 NFs) can effectively catalyze a hydrogen evolution reaction (HER) because of the abundance, ease of processing, and high catalytic activity of MoS2. The main disadvantage of using MoS2 NFs for HER on the industrial scale is their low density and number of active sites. Herein, we propose for the first time a facile, inexpensive, and scalable route for fabricating extremely small MoS2 NFs (SNFs). The size of the synthesized MoS2 SNFs (50–90 nm) is much lower than that of conventional MoS2 NFs (900–1500 nm), which significantly increases the number of catalytically active sites. In addition, the in situ doping of N atoms considerably enhances the catalytic activity of the prepared MoS2 SNFs. MoS2 SNFs exhibit superior electrocatalytic activity toward HER with a low Tafel slope 49 mV·dec−1, an overpotential of 270 mV at a current density of 50 mA·cm−2, a large surface area of 98 m2·g−1, and very high stability in an acidic environment. The obtained results indicate that MoS2 SNFs can be potentially used for energy storage and electrochemical applications.
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