Wang Meng, Sui Xuelei, Wang Yujia, Juan Yung-Hsiang, Lyu Yingjie, Peng Huining, Huang Tongtong, Shen Shengchun, Guo Chenguang, Zhang Jianbing, Li Zhuolu, Li Hao-Bo, Lu Nianpeng, N'Diaye Alpha T, Arenholz Elke, Zhou Shuyun, He Qing, Chu Ying-Hao, Duan Wenhui, Yu Pu
State Key Laboratory of Low Dimensional Quantum Physics and Department of Physics, Tsinghua University, Beijing, 100084, China.
Department of Materials Science and Engineering, National Chiao Tung University, Hsinchu, 30010, Taiwan.
Adv Mater. 2019 Apr;31(16):e1900458. doi: 10.1002/adma.201900458. Epub 2019 Feb 27.
Ionic-liquid-gating- (ILG-) induced proton evolution has emerged as a novel strategy to realize electron doping and manipulate the electronic and magnetic ground states in complex oxides. While the study of a wide range of systems (e.g., SrCoO , VO , WO , etc.) has demonstrated important opportunities to incorporate protons through ILG, protonation remains a big challenge for many others. Furthermore, the mechanism of proton intercalation from the ionic liquid/solid interface to whole film has not yet been revealed. Here, with a model system of inverse spinel NiCo O , an increase in system temperature during ILG forms a single but effective method to efficiently achieve protonation. Moreover, the ILG induces a novel phase transformation in NiCo O from ferrimagnetic metallic into antiferromagnetic insulating with protonation at elevated temperatures. This study shows that environmental temperature is an efficient tuning knob to manipulate ILG-induced ionic evolution.
离子液体门控(ILG)诱导的质子析出已成为一种实现电子掺杂并操控复杂氧化物中电子和磁基态的新策略。虽然对多种体系(如SrCoO、VO、WO等)的研究已证明通过ILG引入质子具有重要机遇,但质子化对许多其他体系而言仍是巨大挑战。此外,质子从离子液体/固体界面插入整个薄膜的机制尚未揭示。在此,以反尖晶石NiCoO的模型体系为例,ILG过程中体系温度的升高形成了一种高效实现质子化的单一但有效的方法。此外,ILG在高温下质子化时会诱导NiCoO发生从亚铁磁性金属相到反铁磁性绝缘相的新型相变。该研究表明环境温度是操控ILG诱导的离子演化的有效调节旋钮。