Superconductivity transition temperature(Tc) marks the inception of a macroscopic quantum phase-coherent paired state in fermionic systems. For 2D superconductivity, the paired electrons condense into a coherent sup...
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Superconductivity transition temperature(Tc) marks the inception of a macroscopic quantum phase-coherent paired state in fermionic systems. For 2D superconductivity, the paired electrons condense into a coherent superfluid state at Tc, which is usually lower than the pairing temperature, between which intrinsic physics including Berezinskii–Kosterlitz–Thouless transition and pseudogap state are hotly debated. In the case of monolayer FeSe superconducting films on SrTiO3(001), although the pairing temperature(Tp) is revealed to be 65–83 K by using spectroscopy characterization, the measured zero-resistance temperature(Tc0) is limited to 20 K. Here, we report significantly enhanced superconductivity in monolayer FeSe films by δ-doping of Eu or Al on SrTiO3(001) surface, in which Tc0is enhanced by 12 K with a narrowed transition width ΔTc~8 K, compared with non-doped samples. Using scanning tunneling microscopy/spectroscopy measurements, we demonstrate lowered work function of the δ-doped SrTiO3(001) surface and enlarged superconducting gaps in the monolayer FeSe with improved morphology/electronic homogeneity. Our work provides a practical route to enhance 2D superconductivity by using interface engineering.
Intercalation transition metal oxides (ITMO)have attracted great attention as lithium-ion battery negative electrodes due to high operation safety,high capacity and rapid ion ***,the intrinsic low electron conductivit...
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Intercalation transition metal oxides (ITMO)have attracted great attention as lithium-ion battery negative electrodes due to high operation safety,high capacity and rapid ion ***,the intrinsic low electron conductivity plagues the lifetime and cell performance of the ITMO negative *** we design a new carbon-emcoating architecture through single CO_(2)activation treatment as demonstrated by the Nb_(2)O_(5)/C *** structure engineering of the carbon-emcoating Nb_(2)O_(5)/C nanohybrid is achieved in terms of porosity,composition,and crystallographic *** carbon-embedding Nb_(2)O_(5)/C nanohybrids show superior cycling and rate performance compared with the conventional carbon coating,with reversible capacity of 387 m A h g(-1)at 0.2 C and 92%of capacity retained after 500cycles at 1 *** electrochemical mass spectrometry(DEMS) indicates that the carbon emcoated Nb_(2)O_(5)nanohybrids present less gas evolution than commercial lithium titanate oxide during *** unique carbon-emcoating technique can be universally applied to other ITMO negative electrodes to achieve high electrochemical performance.
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