Department of Applied Physics and Quantum-Phase Electronics Center (QPEC), University of Tokyo , Tokyo 113-8656, Japan.
RIKEN Center for Emergent Matter Science (CEMS) , Wako, 351-0198, Japan.
ACS Appl Mater Interfaces. 2016 Aug 31;8(34):22330-6. doi: 10.1021/acsami.6b06593. Epub 2016 Aug 16.
An interface between an oxide and an electrolyte gives rise to various processes as exemplified by electrostatic charge accumulation/depletion and electrochemical reactions such as intercalation/decalation under electric field. Here we directly compare typical device operations of those in electric double layer transistor geometry by adopting A-site vacant perovskite WO3 epitaxial thin films as a channel material and two different electrolytes as gating agent. In situ measurements of X-ray diffraction and channel resistance performed during the gating revealed that in both the cases WO3 thin film reaches a new metallic state through multiple phase transitions, accompanied by the change in out-of-plane lattice constant. Electrons are electrostatically accumulated from the interface side with an ionic liquid, while alkaline metal ions are more uniformly intercalated into the film with a polymer electrolyte. We systematically demonstrate this difference in the electrostatic and electrochemical processes, by comparing doped carrier density, lattice deformation behavior, and time constant of the phase transitions.
氧化物和电解质之间的界面会引起各种过程,例如静电电荷积累/耗尽和电化学反应,如电场下的插层/脱层。在这里,我们通过采用 A 位空位钙钛矿 WO3 外延薄膜作为沟道材料和两种不同的电解质作为门控剂,直接比较了具有电双层晶体管几何形状的典型器件操作。在门控过程中进行的 X 射线衍射和沟道电阻的原位测量表明,在这两种情况下,WO3 薄膜通过多次相转变达到新的金属状态,同时伴随面外晶格常数的变化。电子从界面一侧通过离子液体静电积累,而碱性金属离子通过聚合物电解质更均匀地嵌入薄膜中。我们通过比较掺杂载流子密度、晶格变形行为和相变的时间常数,系统地证明了这些静电和电化学过程的差异。