Wang Zhi-Jie, Ni Hao-Fei, Zhang Tie, Li Jie, Lun Meng-Meng, Fu Da-Wei, Zhang Zhi-Xu, Zhang Yi
Ordered Matter Science Research Center, Jiangsu Key Laboratory for Science and Applications of Molecular Ferroelectrics, Southeast University Nanjing 211189 People's Republic of China
Institute for Science and Applications of Molecular Ferroelectrics, Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Zhejiang Normal University Jinhua 321004 People's Republic of China
Chem Sci. 2023 Aug 1;14(34):9041-9047. doi: 10.1039/d3sc02652c. eCollection 2023 Aug 30.
As an innovative form of stimulus-response materials, organic-inorganic hybrid phase transition materials have become a wonderful contender in the field of functional electronic equipment due to their versatile structure, intensive functions and straightforward preparation. However, the targeted regulation and optimization of the electrical/optical response, along with the establishment of regular structure-performance relationships, pose significant challenges in meeting the diverse demands of practical applications over an extended period. Herein, we conducted a systematic investigation into the role of lattice void occupancy in regulating phase transition temperature () and related optical/electrical bistability. By taking hybrid material [TMEA][Cd(SCN)] featuring a flexible ammonium cation [TMEA] (TMEA = ethyltrimethylammonium) as the prototype, we successfully synthesized three phase transition materials, namely [DEDMA][Cd(SCN)], [TEMA][Cd(SCN)] and [TEA][Cd(SCN)] (DEDMA = diethyldimethylammonium, TEMA = triethylmethylammonium, and TEA = tetraethylammonium), and the excellent regulation of the physical properties of these compounds was achieved through subtle engineering of void occupancy. More strikingly, [TEA][Cd(SCN)] exhibits remarkable bistable properties in terms of dielectric and nonlinear optical responses (with second-harmonic generation intensity reaching 2.5 times that of KDP). This work provides a feasible avenue to reasonably customise organic-inorganic hybrid phase transition materials and finely adjust their intriguing functionalities.
作为一种创新的刺激响应材料形式,有机-无机杂化相变材料因其结构多样、功能丰富且制备简便,已成为功能电子设备领域的有力竞争者。然而,对其电学/光学响应进行靶向调控与优化,以及建立规则的结构-性能关系,在长期满足实际应用的多样化需求方面面临重大挑战。在此,我们对晶格空位占有率在调节相变温度()及相关光学/电学双稳性中的作用进行了系统研究。以具有柔性铵阳离子[TMEA](TMEA = 乙基三甲基铵)的杂化材料[TMEA][Cd(SCN)]为原型,我们成功合成了三种相变材料,即[DEDMA][Cd(SCN)]、[TEMA][Cd(SCN)]和[TEA][Cd(SCN)](DEDMA = 二乙基二甲基铵,TEMA = 三乙基甲基铵,TEA = 四乙基铵),并通过对空位占有率的精细调控实现了对这些化合物物理性质的优异调控。更引人注目的是,[TEA][Cd(SCN)]在介电和非线性光学响应方面表现出显著的双稳性(二次谐波产生强度达到KDP的2.5倍)。这项工作为合理定制有机-无机杂化相变材料并精细调节其有趣功能提供了一条可行途径。