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This letter reports the implementation of double-drift-layer (DDL) design into GaN vertical Schottky barrier diodes (SBDs) grown on free-standing GaN substrates. This design balances the trade-off between desirable forward turn-on characteristics and high reverse breakdown capability, providing optimal overall device performances for power switching applications. With a wellcontrolled metalorganic chemical vapor deposition process, the doping concentration of the top drift layer was reduced, which served to suppress the peak electric field at the metal/GaN interface and increase the breakdown voltages of the SBDs. The bottom drift layer was moderately doped to achieve low on-resistance to reduce power losses. At forward bias, the devices exhibited a record low turn-on voltage of 0.59 V, an ultra-low on-resistance of 1.65 mX cm 2 , a near unity ideality factor of 1.04, a high on/off ratio of $10 10 , and a high electron mobility of 1045.2 cm 2 /(V s). Detailed comparisons with conventional single-drift-layer (SDL) GaN vertical SBDs indicated that DDL design did not degrade the forward characteristics of the SBDs. At reverse bias, breakdown voltages of the DDL GaN SBDs were considerably enhanced compared to those of the conventional SDL devices. These results showed that GaN vertical SBDs with DDL designs are promising candidates for high efficiency, high voltage, high frequency power switching applications.

The key factors governing the single-phase or multi-phase structural change behaviors during the intercalation/deintercalation of guest ions have not been well studied and understood yet. Through systematic studies of orthorhombic Fe2(MoO4)3 electrode, two distinct guest ion occupation paths, namely discrete one for Li and pseudo-continuous one for Na, as well as their relationship with single-phase and two-phase modes for Na+ and Li+, respectively during the intercalation/deintercalation process have been demonstrated. For the first time, the direct atomic-scale observation of biphasic domains (discrete occupation) in partially lithiated Fe2(MoO4)3 and the one by one Na occupation (pseudo-continuous occupation) at 8d sites in partially sodiated Fe2(MoO4)3 are obtained during the discharge processes of Li/Fe2(MoO4)3 and Na/Fe2(MoO4)3 cells respectively. Our combined experimental and theoretical studies bring the new insights for the research and development of intercalation compounds as electrode materials for secondary batteries.

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In this paper, we perform a comprehensive study on energy band engineering of InGaN multi-quantum-well (MQW) solar cells using AlGaN electron- and hole-blocking layers. InGaN MQW solar cells with AlGaN layers were grown by metalorganic chemical vapor deposition, and high crystal quality was confirmed by high resolution X-ray diffraction measurements. Time-resolved photoluminescence results showed that the carrier lifetime on the solar cells with AlGaN layers increased by more than 40% compared to that on the reference samples, indicating greatly improved carrier collections. The illuminated current-density (J–V) measurements further confirmed that the short-circuit current density (Jsc) of the solar cells also benefited from the AlGaN layer design and increased 46%. At room temperature, the InGaN solar cells with AlGaN layers showed much higher power conversion efficiency (PCE), by up to two-fold, compared to reference devices. At high temperatures, these solar cells with AlGaN layers also delivered superior photovoltaic (PV) performance such as PCE, Jsc, and fill factor than the reference devices. These results indicate that band engineering with AlGaN layers in the InGaN MQW solar cell structures can effectively enhance the carrier collection process and is a promising design for high efficiency InGaN solar cells for both room temperature and high temperature PV applications.