Close Menu
    Facebook X (Twitter) Instagram
    SciTechDaily
    • Biology
    • Chemistry
    • Earth
    • Health
    • Physics
    • Science
    • Space
    • Technology
    Facebook X (Twitter) Pinterest YouTube RSS
    SciTechDaily
    Home»Chemistry»Ultrafast Polaronic Exciton Dissociation Mechanism in 2D Perovskites
    Chemistry

    Ultrafast Polaronic Exciton Dissociation Mechanism in 2D Perovskites

    By Dalian Institute of Chemical PhysicsNovember 29, 2021No Comments3 Mins Read
    Facebook Twitter Pinterest Telegram LinkedIn WhatsApp Email Reddit
    Share
    Facebook Twitter LinkedIn Pinterest Telegram Email Reddit
    Ultrafast Exciton Dissociation Mechanism in 2D Perovskites
    Excitons in two-dimensional perovskites rapidly dissociate into free carriers beneficial for photovoltaic applications, just as bees holding electrons and holes meet and separate in the flowers. Credit: DICP

    Researchers have uncovered an ultrafast and highly efficient exciton dissociation process in 2D perovskites, overturning long-standing assumptions.

    A research group led by Prof. JIN Shengye from the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences revealed an ultrafast and high-yield polaronic exciton dissociation mechanism in two-dimensional (2D) perovskites.

    This study was published in Journal of the American Chemical Society on November 3, 2021.  

    2D perovskites are a class of naturally formed quantum well (QW) materials. The exciton binding energy in 2D perovskite is much larger (up to hundreds of meV) than that in their 3D counterparts due to strong quantum and dielectric confinement.

    Therefore, it is commonly believed that the photogenerated charge carriers in 2D perovskites mainly exist in the form of excitons, which are difficult to dissociate into free carriers at room temperature.

    In this study, by using femtosecond photoluminescence up-conversion (PL-UC) and transient absorption (TA) spectroscopy, the researchers for the first time directly and dynamically observed the ultrafast (< 1.4 ps) and highly efficient (> 80%) exciton dissociation in 2D perovskites (n ≥ 2). This confirmed that free-carriers were the dominant carrier species in 2D perovskites under room temperature, which conflicts with previous thought.

    Polaron-Induced Mechanism Unlocks Dissociation

    Moreover, they proposed a polaron-induced exciton dissociation mechanism, where the exciton-polarons were readily formed by strong exciton-phonon coupling as in 3D perovskites, and the polaronic screening effect led to a prominent reduction in binding energy for efficient exciton dissociation.

    The researchers demonstrated that the exciton dissociation into free-carriers was a major factor limiting the photoluminescence quantum yield of 2D perovskites by introducing additional nonradiative carrier loss.

    “This work reveals a common exciton dissociation property in this class of 2D materials and provides a guideline for the design and rational utilization of 2D perovskites in optical and optoelectronic applications,” said Prof. JIN.

    Reference: “Ultrafast and High-Yield Polaronic Exciton Dissociation in Two-Dimensional Perovskites” by Qi Sun, Chunyi Zhao, Zixi Yin, Shiping Wang, Jing Leng, Wenming Tian and Shengye Jin, 3 November 2021, Journal of the American Chemical Society.
    DOI: 10.1021/jacs.1c08900

    This study was supported by the Ministry of Science and Technology of China, the National Natural Science Foundation of China and the Youth Innovation Promotion Association of CAS.

    Never miss a breakthrough: Join the SciTechDaily newsletter.
    Follow us on Google and Google News.

    Chinese Academy of Sciences Nanotechnology
    Share. Facebook Twitter Pinterest LinkedIn Email Reddit

    Related Articles

    How Scientists Are Using Atomic Precision to Supercharge Chemistry

    Photonic Cellulose Nanocrystal Sensor Revolutionizes Biomedical Monitoring

    Researchers Capture Electron Transfer Image in Electrocatalysis Process

    Catalytic Hydrogenation of CO2 to Methanol: Low Temperature and High Efficiency

    Scientists Examine Platinum-Based Catalyst Design

    Artificial System Models Light-Capturing Method Used by Deep-Sea Bacteria

    Zeolite Catalyst Creates P-Xylene From Biomass

    Gold Nanorods Shaped as Starfruit Deliver Impressive Results

    Gold Improves the Performance of Nanoparticle Fuel-Cell Reactions

    Leave A Reply Cancel Reply

    • Facebook
    • Twitter
    • Pinterest
    • YouTube

    Don't Miss a Discovery

    Subscribe for the Latest in Science & Tech!

    Trending News

    Tea or Coffee? Your Daily Choice Could Affect Osteoporosis Risk

    Vitamin C May Fight Cancer in a Surprising Way

    Hidden Earthquake Threat: Oregon’s Fault May Be Closer to the Surface Than Scientists Thought

    Scientists Discover Hidden Sleep Switch That Boosts Brainpower, Builds Muscle, and Burns Fat

    Ancient Mega-Floods Once Ripped Across Mars and Left This Giant Scar

    Scientists Discover Cheap, Natural Remedy for High Blood Pressure

    Earth’s Upper Atmosphere Is Cooling Fast and Scientists Finally Know Why

    32,000 Olympic Pools of Magma Nearly Erupted Beneath Atlantic Island

    Follow SciTechDaily
    • Facebook
    • Twitter
    • YouTube
    • Pinterest
    • Newsletter
    • RSS
    SciTech News
    • Biology News
    • Chemistry News
    • Earth News
    • Health News
    • Physics News
    • Science News
    • Space News
    • Technology News
    Recent Posts
    • The Type of Alcohol You Drink Could Affect How Long You Live
    • 19-Year Study Reveals the Surprising Truth About Sitting and Dementia
    • This Common Vitamin May Help Stop Prediabetes From Turning Into Diabetes
    • Canada’s Billion-Year-Old Rocks Could Hold the Future of Clean Energy
    • Climate Change Is Quietly Choking Rivers Across the Planet
    Copyright © 1998 - 2026 SciTechDaily. All Rights Reserved.
    • Science News
    • About
    • Contact
    • Editorial Board
    • Privacy Policy
    • Terms of Use

    Type above and press Enter to search. Press Esc to cancel.