溶解
激进的
二硫化钼
密度泛函理论
钼
化学
过渡金属
降级(电信)
分子动力学
光化学
化学物理
从头算
化学工程
计算化学
材料科学
无机化学
催化作用
物理化学
有机化学
计算机科学
工程类
电信
作者
Dashi Lei,Zhongyi Wu,Yu Zhang,Yiyao Zhang,Jing Zhang,Juanqin Xue,Xiangyu Peng,Yubin Wang
标识
DOI:10.1016/j.seppur.2023.125800
摘要
The long-term persistence of transition metal dichalcogenide (TMD) gets severely weakened at humid environments, which is key issue to solve in application. However, previous studies about TMD oxidation mainly focused under light irradiation, while lack of exploration at dark environments. Herein, we filled the gap in research of the oxidation and dissolution behaviors of TMD, represented by molybdenum disulfide (MoS2). under dark condition. The results demonstrate that water and oxygen could react produce hydroxyl radicals (•OH) on MoS2 interface, a critical intermedia for MoS2 oxidation and dissolution. Ab-initio molecular dynamics (AIMD) simulations present detailed formation process of •OH over MoS2 surface, and spin-polarized density functional theory (DFT) calculations confirm its generation. While, under basic conditions, AIMD and DFT calculations demonstrated the generation of H2O2 at MoS2 hydroxylated surface. This work will assist in understanding of MoS2 oxidation and dissolution behavior, and provide references for the investigation of long-term stability of TMDs.
科研通智能强力驱动
Strongly Powered by AbleSci AI