An Ran, Wang Qishun, Liang Yuan, Du Pengye, Lei Pengpeng, Sun Haizhu, Wang Xinyu, Feng Jing, Song Shuyan, Zhang Hongjie
Faculty of Chemistry, Northeast Normal University, Jilin, Changchun, 130024, China E-mail: addresses.
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Jilin, Changchun, 130022, China.
Angew Chem Int Ed Engl. 2025 Jan 2;64(1):e202413991. doi: 10.1002/anie.202413991. Epub 2024 Oct 29.
Exploring structural phase transitions and luminescence mechanisms in zero-dimensional (0D) metal halides poses significant challenges, that are crucial for unlocking the full potential of tunable optical properties and diversifying their functional capabilities. Herein, we have designed two inter-transformable 0D Cu(I)-based metal halides, namely (CHP)CuI and (CHP)CuI, through distinct synthesis conditions utilizing identical reactants. Their optical properties and luminescence mechanisms were systematically elucidated by experiments combined with density functional theory calculations. The bright cyan-fluorescent (CHP)CuI with high photoluminescence quantum yield (PLQY) of 77 % is attributed to the self-trapped exciton emission. Differently, the broad yellow-orange fluorescence of (CHP)CuI displays a remarkable PLQY of 83 %. Its luminescence mechanism is mainly attributed to the combined effects of metal/halide-to-ligand charge transfer and cluster-centered charge transfer, which effects stem from the strong Cu-Cu bonding interactions in the (CuI) clusters. Moreover, (CHP)CuI and (CHP)CuI exhibit reversible structural phase transitions. The elucidation of the phase transitions mechanism has paved the way for an unforgeable anti-counterfeiting system. This system dynamically shifts between cyan and yellow-orange fluorescence, triggered by the phase transitions, bolstering security and authenticity. This work enriches the luminescence theory of 0D metal halides, offering novel strategies for optical property modulation and fostering optical applications.
探索零维(0D)金属卤化物中的结构相变和发光机制面临重大挑战,这些挑战对于释放可调光学性质的全部潜力并使其功能能力多样化至关重要。在此,我们通过使用相同反应物的不同合成条件设计了两种可相互转化的基于0D Cu(I)的金属卤化物,即(CHP)CuI和(CHP)CuI。通过实验结合密度泛函理论计算系统地阐明了它们的光学性质和发光机制。具有77%高光致发光量子产率(PLQY)的明亮青色荧光(CHP)CuI归因于自陷激子发射。不同的是,(CHP)CuI的宽黄橙色荧光显示出83%的显著PLQY。其发光机制主要归因于金属/卤化物到配体的电荷转移和簇中心电荷转移的综合作用,这些作用源于(CuI)簇中强烈的Cu-Cu键相互作用。此外,(CHP)CuI和(CHP)CuI表现出可逆的结构相变。相变机制的阐明为不可伪造的防伪系统铺平了道路。该系统由相变触发,在青色和黄橙色荧光之间动态切换,增强了安全性和真实性。这项工作丰富了0D金属卤化物的发光理论,为光学性质调制提供了新策略,并促进了光学应用。