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Trap analysis of composite 2D-3D channel in AlGaN/GaN/graded-AlGaN:Si/GaN:C multi-heterostructure at different temperatures
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作者 Sheng Hu Ling Yang +12 位作者 Min-Han Mi Bin Hou Sheng Liu Meng Zhang Mei Wu Qing Zhu Sheng Wu Yang Lu Jie-Jie Zhu Xiao-Wei Zhou Ling Lv Xiao-Hua Ma Yue Hao 《Chinese Physics B》 SCIE EI CAS CSCD 2020年第8期451-456,共6页
The graded AlGaN:Si back barrier can form the majority of three-dimensional electron gases(3DEGs)at the GaN/graded AlGaN:Si heterostructure and create a composite two-dimensional(2D)-three-dimensional(3D)channel in Al... The graded AlGaN:Si back barrier can form the majority of three-dimensional electron gases(3DEGs)at the GaN/graded AlGaN:Si heterostructure and create a composite two-dimensional(2D)-three-dimensional(3D)channel in AlGaN/GaN/graded-AlGaN:Si/GaN:C heterostructure(DH:Si/C).Frequency-dependent capacitances and conductance are measured to investigate the characteristics of the multi-temperature trap states of in DH:Si/C and AlGaN/GaN/GaN:C heterostructure(SH:C).There are fast,medium,and slow trap states in DH:Si/C,while only medium trap states exist in SH:C.The time constant/trap density for medium trap state in SH:C heterostructure are(11μs-17.7μs)/(1.1×10^13 cm^-2·eV^-1-3.9×10^13 cm^-2·eV^-1)and(8.7μs-14.1μs)/(0.7×10^13 cm^-2·eV^-1-1.9×10^13 cm^-2·eV^-1)at 300 K and 500 K respectively.The time constant/trap density for fast,medium,and slow trap states in DH:Si/C heterostructure are(4.2μs-7.7μs)/(1.5×10^13 cm^-2·eV^-1-3.2×10^13 cm^-2·eV^-1),(6.8μs-11.8μs)/(0.8×10^13 cm^-2·eV^-1-2.8×10^13 cm^-2·eV^-1),(30.1μs-151μs)/(7.5×10^12 cm^-2·eV^-1-7.8×10^12 cm^-2·eV^-1)at 300 K and(3.5μs-6.5μs)/(0.9×10^13 cm^-2·eV^-1-1.8×10^13 cm^-2·eV^-1),(4.9μs-9.4μs)/(0.6×10^13 cm^-2·eV^-1-1.7×10^13 cm^-2·eV^-1),(20.6μs-61.9μs)/(3.2×10^12 cm^-2·eV^-1-3.5×10^12 cm^-2·eV^-1)at 500 K,respectively.The DH:Si/C structure can effectively reduce the density of medium trap states compared with SH:C structure. 展开更多
关键词 AlGaN/GaN HEMT multi-heterostructure composite 2D-3D channel multi-temperature trap states
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Achieving high-proportioned 1T-MoS_(2)within heterostructures derived from polymolybdate-based complex for boosting electrocatalytic hydrogen evolution and oxygen evolution
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作者 Zhihan Chang Yuchen Zhang +1 位作者 Yuan Tian Xiuli Wang 《Chinese Chemical Letters》 2025年第8期478-486,共9页
The fabrication of bifunctional electrocatalysts for hydrogen and oxygen evolution in aqueous environment has far-reaching significance.Especially,reasonable interface process regulation toward heterogeneous composite... The fabrication of bifunctional electrocatalysts for hydrogen and oxygen evolution in aqueous environment has far-reaching significance.Especially,reasonable interface process regulation toward heterogeneous composites can make full use of the active sites and improve the electrocatalytic activity.In this study,we designed and synthesized NiS_(2)-MoS_(2)-based heterogeneous composites as efficient and stable electrocatalysts for hydrogen and oxygen evolution in alkaline electrolyte.The heterostructure was obtained by one-step hydrothermal ulfurization operation towards polymolybdate-based metal-organic complex.The composition and nanostructures can be tailored by modulating experiment parameter,realizing the phase-controlled synthesis and interface regulation:(1)High-percentage of 1T-MoS_(2)can be achieved via selecting appropriate vulcanization time and thiourea concentration,benifiting for the higher electroconductivity and more active sites;(2)Regular and orderly vulcanization time promotes the gradual growth and aggregation of nanosheets;(3)The existence of nickel hydroxide improves the electrocatalytic stability for oxygen production performance.The optimized heterogeneous interfaces provide sufficient active sites and accelerate electron transfer.Consequently,the optimal heterogeneous nanosheets present low overpotentials of 33 and 122 m V at the catalytic current densities of 10 m A/cm2for HER and OER,respectively. 展开更多
关键词 POLYMOLYBDATE multi-heterostructure POLYOXOMETALATES Electrocatalytic hydrogen/oxygen evolution Metal-organic complexes
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