超短脉冲
材料科学
超快激光光谱学
电场
反应性(心理学)
单层
纳米尺度
电子
吸收(声学)
化学物理
光电子学
吸收光谱法
超快电子衍射
光谱学
催化作用
领域(数学)
光化学
分子物理学
纳米技术
Crystal(编程语言)
纳米电子学
电子转移
瞬态(计算机编程)
电化学
电子定域函数
金属
电子传输链
单晶
过渡金属
电子迁移率
皮秒
自组装单层膜
作者
Feng Li,Qi Sun,Tao Yang,Fengke Sun,Boning Wu,Shengye Jin,Wenming Tian
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-08-12
卷期号:12 (33): eaee0180-eaee0180
标识
DOI:10.1126/sciadv.aee0180
摘要
Monolayer MoS 2 is a promising low-cost and efficient catalyst for electrochemical or photochemical reduction reactions. Many previous works have demonstrated that 2D MoS 2 edges or boundaries are active reaction sites; however, their structural and electron dynamic origins remain unclear. Here we report an aperture-type near-field ultrafast transient absorption spectroscopy to directly probe the electron dynamics at nanoscale MoS 2 boundaries. Near-field transient absorption imaging reveals a Stark effect signature at boundaries, where a built-in electric field of 1.93 MV/cm is intrinsically formed due to the oxidation of crystal boundaries. This field drives ultrafast electron injection and accumulation at the boundaries, enhancing boundary reactivity over the interior. These findings uncover the nanoscale structure-activity correlation for 2D MoS 2 and promote the rational design of catalysts based on transition metal dichalcogenides.
科研通智能强力驱动
Strongly Powered by AbleSci AI