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Updated: Aug 14, 2026

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Internal electric fields enhance reductive reactivity at MoS2 boundaries revealed by ultrafast near-field
Feng Li1,2, Qi Sun1, Tao Yang1
1State Key Laboratory of Chemical Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences; Dalian 116023, China.
Abstract:
Monolayer MoS2 is a promising low-cost and efficient catalyst for electrochemical or photochemical reduction reactions. Many previous works have demonstrated that 2D MoS2 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 MoS2 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 MoS2 and promote the rational design of catalysts based on transition metal dichalcogenides.
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