1992
DOI: 10.1039/jm9920200031
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Predominant defects in semiconductor isovalent solid solutions: Pb1 –y(SexTe1 –x)y, Pb1 –y(SxTe1 –x)yand Pb1 –y(SxSe1 –x)y

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Cited by 19 publications
(20 citation statements)
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“…In addition, most reported vanadium-based cathodes are synthesized by hydrothermal or annealing methods, and the products usually have high crystallinity. [16][17][18][19][20] The intercalation/ deintercalation of Zn 2+ in the crystal framework can only proceed along specic routes and is stored in certain active sites, resulting in sluggish reaction kinetics and insufficient specic capacity. And the specic capacity decays rapidly due to the collapse of the rigid crystal framework caused by "volume expansion" during repeated Zn 2+ intercalation.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, most reported vanadium-based cathodes are synthesized by hydrothermal or annealing methods, and the products usually have high crystallinity. [16][17][18][19][20] The intercalation/ deintercalation of Zn 2+ in the crystal framework can only proceed along specic routes and is stored in certain active sites, resulting in sluggish reaction kinetics and insufficient specic capacity. And the specic capacity decays rapidly due to the collapse of the rigid crystal framework caused by "volume expansion" during repeated Zn 2+ intercalation.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the successful optimization of the material composition, the SPU 1.2 /30%IL 0.5 ionogels achieved the highest Δ T sol and T lum among all reported thermochromic materials (Figure 3e). [ 23,45–57 ] As shown in Figure 3f, the thermochromic performance of the SPU 1.2 /30%IL 0.5 ionogel, including T lum , T sol , luminous modulation capability (Δ T lum ) and Δ T sol , were well maintained after 1000 cycles of heating to 40 °C and cooling to room temperature. Furthermore, the ionogel's thermochromic performance remained unchanged after 1000 cycles of stretching to 150% of its original length and releasing, being stored at −30 °C, 60 °C, 90% RH, and vacuum environments (relative vacuum pressure = −0.098 MPa) for 2 months, and 1000 cycles of 180° bending and flattening (Figure 3f).…”
Section: Resultsmentioning
confidence: 95%
“…The reser voirs containing B and C source materials are con nected to a vessel containing (A 1 -x B x ) 1 -δ C 1 + δ by capillary tubes, which prevents rapid transport of com ponents B and C. Similar configurations can be used for melt or vapor growth of nonstoichiometric ternary compounds. At the same time, one can use a two component, two phase mixture, which ensures appro priate vapor pressures of both components at a con stant temperature [40,42]. [43,44].…”
Section: Nonstoichiometry Control During Crystal Growthmentioning
confidence: 99%