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Detian Yang

Publications and source records attributed to Detian Yang.

6 recordsLinked to original sources

Thickness-Driven Superconductor-Insulator Transition in (Cu,C)-1234 and Proximity-Induced Superconductivity Recovery in (Cu,C)-1234/YBCO Heterostructure

Superconducting proximity effect and related thickness-driven property evolution remain an important issue in understanding high temperature superconductors. Among proximity systems, superconductor-superconductor (S-S') is special for the existence of intrinsic superconductivity in both materials. Such platform allows the different superconducting orders to compete, couple and reconstruct at the interface. In this paper, (Cu,C)-1234/YBCO heterostructure grown on LAO (001) with fixed thickness of bottom YBCO layer as 150 nm and varied thickness of top (Cu,C)-1234 layer as 188nm, 87 nm, 18nm and estimated 1.2 nm were fabricated and component films were preserved. Electrical transport characterization indicated that as the thickness decrease the (Cu,C)-1234 film degrades and underwent the superconductor-insulator transition (SIT) from thicker to less than 18 nm. In contrast, superconductivity is re-established in transport measurements when the insulating (Cu,C)-1234 layer is coupled to superconducting YBCO As the (Cu,C)-1234 thickness is further reduced to approximately 1.2 nm, the recovered superconductivity is strongly suppressed. The observed thickness dependence is consistent with a scenario in which interfacial coupling restores superconductivity over a finite thickness range before increasing disorder and dimensional confinement dominate in the two-dimensional limit. This work establishes a promising platform for investigating interfacial coupling between cuprate superconductors and provides new insight into the superconducting proximity effect in high-temperature superconducting heterostructures.

cond-mat.supr-con

Billion-Fold Enhancement of Room-Temperature Ionic Conductivity in h-RMnO3/YSZ Heterostructures via Electric-Field-Assisted Oxygen Deficiency Engineering

Oxide heterostructures provide versatile platforms for manipulating electronic and ionic conductive states. In this study, we demonstrate a remarkable billion-fold enhancement in room-temperature ionic conductivity within h-RMnO3/YSZ heterostructures, achieved through electric-field-assisted oxygen deficiency engineering. This enhancement is closely linked to substantial oxygen depletion in YSZ and is tunable by varying the thickness of the h-RMnO3 film layer and the applied voltage bias. Our findings underscore the critical importance of interfacial design and vacancy control in enhancing ionic transport capabilities, paving the way for advanced applications in low-temperature energy harvesting, storage, and conversion technologies.

cond-mat.mtrl-sci

Enhance Ferroelectric Structural Distortion via Doping Ca in Epitaxial h-Lu1-xCaxMnO3 Thin Films

Unlike proper ferroelectricity, the improper ferroelectricity in multiferroic rare-earth manganites h-ReMnO3 (Re=La-Lu,Y,Sc) thin films features a unique geometric distortion and stays immune to the depolarizing field in the ultra-thin limit. Here, we have managed to tune and boost ferroelectric geometric distortion of h-LuMnO3 thin films by doping Ca. Compressively strained h-Lu1-xCaxMnO3(x=0.1,0.2,0.3,0.4,0.5)epitaxial thin films were stabilized over sapphire substrates by a h-ScFeO3 buffer layer. When the doping concentration x>=0.2, the common substrate-induced interface clamping effect that suppresses improper ferroelectricity of h-ReMnO3 can be eliminated. This work establishes a potential quasi-2D ferroelectric system and suggests a general strain engineering method to enhance improper ferroelectricity of hexagonal manganites.

cond-mat.mtrl-sci

Dual mechanisms for transient capacitance anomaly in improper ferroelectrics

The recent discovery of transient negative capacitance has sparked an intense debate on the role of homogeneous and inhomogeneous mechanisms in polarizations switching. In this work, we report observation of transient negative capacitance in improper ferroelectric h-YbFeO3 films in a resistor-capacitor circuit, and a concaved shape of anomaly in the voltage wave form, in the early and late stage of the polarizations switching respectively. Using a phenomenological model, we show that the early-stage negative capacitance is likely due to the inhomogeneous switching involving nucleation and domain wall motion, while the anomaly at the late stage, which appears to be a reminiscent negative capacitance is the manifestation of the thermodynamically unstable part of the free-energy landscape in the homogeneous switching. The complex free-energy landscape in hexagonal ferrites may be the key to cause the abrupt change in polarization switching speed and the corresponding anomaly. These results reconcile the two seemingly conflicting mechanisms in the polarization switching and highlight their different roles at different stages. The unique energy-landscape in hexagonal ferrites that reveals the dual switching mechanism suggests the promising application potential in terms of negative capacitance.

cond-mat.mtrl-sci

Intrinsic Exchange Bias from Interfacial Reconstruction in an Epitaxial NixCoyFe3-x-yO4(111)/{\alpha}-Al2O3(0001) Thin Film Family

Intrinsic exchange bias is known as the unidirectional exchange anisotropy that emerges in a nominally single-component ferro-(ferri-)magnetic system. In this work, with magnetic and structural characterizations, we demonstrate that intrinsic exchange bias is a general phenomenon in (Ni, Co, Fe)-based spinel oxide films deposited on {\alpha}-Al2O3(0001) substrates, due to the emergence of a rock-salt interfacial layer consisting of antiferromagnetic CoO from interfacial reconstruction. We show that in NixCoyFe3-x-yO4(111)/{\alpha}-Al2O3(0001) films, intrinsic exchange bias and interfacial reconstruction have consistent dependences on Co concentration y, while the Ni and Fe concentration appears to be less important. This work establishes a family of intrinsic exchange bias materials with great tunability by stoichiometry and highlights the strategy of interface engineering in controlling material functionalities.

cond-mat.mtrl-sci

Colossal intrinsic exchange bias in epitaxial CoFe2O4/Al2O3 thin films

In this work, we demonstrate a massive intrinsic exchange bias (3 kOe) in epitaxial CoFe2O4(111) thin films deposited on Al2O3(0001) substrates. This exchange bias is indicative of intrinsic exchange or a ferromagnetic material combined with an antiferromagnet. The analysis of structure, magnetism and electronic states corroborate that there is an interfacial layer CoO between the CoFe2O4(111) thin film and the Al2O3(0001) substrate. The power-law thickness dependence of the intrinsic exchange bias verifies its interfacial origin. This work suggests interfacial engineering can be an effective route for achieving large exchange bias.

cond-mat.mtrl-sci