反铁电性
材料科学
电介质
极化(电化学)
磁滞
储能
居里温度
铁电性
金属
工作(物理)
化学物理
纳米技术
光电子学
凝聚态物理
化学
热力学
物理化学
物理
铁磁性
功率(物理)
冶金
作者
Haojie Xu,Wuqian Guo,Yu Ma,Yi Liu,Xinxin Hu,Lina Hua,Shiguo Han,Xitao Liu,Junhua Luo,Zhihua Sun
标识
DOI:10.1038/s41467-022-33039-9
摘要
Metal-free antiferroelectric materials are holding a promise for energy storage application, owing to their unique merits of wearability, environmental friendliness, and structure tunability. Despite receiving great interests, metal-free antiferroelectrics are quite limited and it is a challenge to acquire new soft antiferroelectric candidates. Here, we have successfully exploited binary CMBrxI1-x and CMBrxCl1-x solid solution as single crystals (0 ≤ x ≤ 1, where CM is cyclohexylmethylammonium). A molecule-level modification can effectively enhance Curie temperature. Emphatically, the binary CM-chloride salt shows the highest antiferroelectric-to-paraelectric Curie temperature of ~453 K among the known molecular antiferroelectrics. Its characteristic double electrical hysteresis loops provide a large electric polarization up to ~11.4 μC/cm2, which endows notable energy storage behaviors. To our best knowledge, this work provides an effective solid-solution methodology to the targeted design of new metal-free antiferroelectric candidates toward biocompatible energy storage devices.
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