相变
材料科学
原子物理学
放射化学
核物理学
化学
凝聚态物理
物理
作者
Zhenyu Wang,Chaoqun Gu,Sisi Jiang,Tong Sun,Zonghua Wang
标识
DOI:10.1088/1361-648x/acd219
摘要
The mixed-phase MoS2(1T/2H MoS2) with heterostructure exhibited high catalytic activity. The specific ratios of 1T/2H could exhibit optimal performance in various applications. Therefore, more methods need be developed for synthesizing 1T/2H mixed-phase MoS2. Herein, a viable route was studied for the phase transition of 1T/2H MoS2regulated by H+. Briefly, the commercially available bulk MoS2was used to obtain 1T/2H MoS2via chemical intercalation of Li+. Then the residual Li+around 1T/2H MoS2was replaced by H+in acidic electrolytes, owing to the extremely higher charge-to-volume ratio of H+. Thus, the thermodynamically unstable 1T phase lost the protection of residual Li+and could be re-transforming into the relatively stable 2H phase. The change of the 2H/(2H+1T) ratio was measured using novel extinction spectroscopy, which provides a rapid identification method in comparison with x-ray photoelectron spectroscopy (XPS). The experimental results revealed that the concentration of H+influenced the phase transition velocity of MoS2. In particular, the phase transition from 1T to 2H phase in the H+solution was faster at the beginning, and the higher the H+concentration in an acidic solution, the faster the increase in 2H content. For an instant, the ratio of the 2H phase was increased by 7.08% in an acidic solution (CH+= 2.00 M) after 1 h, which was several times greater than the case in the distilled water. This finding provides a promising method to easily obtain different ratios of 1T/2H MoS2, which is beneficial for further development of catalytic performance especially in energy generation and storage.
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