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晶体生长的热动力学分析——以碘化汞晶体为例
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作者 陈静 《当代化工研究》 CAS 2024年第9期41-43,共3页
为研究热动力学因素对晶体形貌的影响,以碘化汞晶体为例,对晶体生长速率进行分析计算,得到台阶能、面溶解焓、体溶解焓、有效溶质的摩尔分数以及各晶面的生长速率,根据α-HgI_(2)晶体的各晶面的生长速率排序(001)<(110)<(101)<... 为研究热动力学因素对晶体形貌的影响,以碘化汞晶体为例,对晶体生长速率进行分析计算,得到台阶能、面溶解焓、体溶解焓、有效溶质的摩尔分数以及各晶面的生长速率,根据α-HgI_(2)晶体的各晶面的生长速率排序(001)<(110)<(101)<(102)<(103),确定(001)面应为α-HgI_(2)晶体的最大显露面,体现出了α-HgI_(2)晶体的最大形态学特征。 展开更多
关键词 晶体形貌 碘化汞 热动力学因素 晶体生长速率
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Effect of Phosphate on Zinc Transport in Lou Soil 被引量:4
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作者 LU JIALONG DONG LINGXIAO +1 位作者 ZHANG YIPING ZHANG FUCANG and PAN ZHI (Department of Resources and Environmental Sciences, Northwestern Agricultural University, Yangling,Shaanxi 712100 China) 《Pedosphere》 SCIE CAS CSCD 1998年第4期355-360,共6页
A study on the transport characteristics of zinc in lou soil with phosphate at different concentrations was carried out by the method of step input. The effects of phosphate and temperature on zinc transport were stud... A study on the transport characteristics of zinc in lou soil with phosphate at different concentrations was carried out by the method of step input. The effects of phosphate and temperature on zinc transport were studied through analysing the diffusion-dispersion coefficients (D) and the retardation factor (R) obtained by the program CXTFIT. The results showed that D decreased and R increased with increasing concentration of phosphate so that it was difficult for zinc to break through the soil column, and zinc stopped to break through the column at high temperature. One order equation, double constant equation and the Elovich equation were all suitable for the description of zinc dynamica. Effects of phosphate and temperature on zinc transport were further confirmed by the analysis on pseudo-thermodynamic parameters of zinc transport. 展开更多
关键词 diffusion-dispersion coefficient PHOSPHATE pseudo-thermodynamic parameters retardation factor zinc transport kinetics
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Cationic-potential tuned biphasic layered cathodes for stable desodiation/sodiation 被引量:1
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作者 Xu Gao Huanqing Liu +17 位作者 Hongyi Chen Yu Mei Baowei Wang Liang Fang Mingzhe Chen Jun Chen Jinqiang Gao Lianshan Ni Li Yang Ye Tian Wentao Deng Roya Momen Weifeng Wei Libao Chen Guoqiang Zou Hongshuai Hou Yong-Mook Kang Xiaobo Ji 《Science Bulletin》 SCIE EI CAS CSCD 2022年第15期1589-1602,M0004,共15页
Sodium layered oxides generally suffer from deep-desodiation instability in P2 structure and sluggish kinetics in O3 structure.It will be great to design P2/O3 biphasic materials that bring the complementary merits of... Sodium layered oxides generally suffer from deep-desodiation instability in P2 structure and sluggish kinetics in O3 structure.It will be great to design P2/O3 biphasic materials that bring the complementary merits of both structures.However,such exploration is hindered by the ambiguous mechanism of material formation.Herein,supported by theoretical simulations and various spectroscopies,we prove that P2/O3 biphasic structures essentially originate from the internal heterogeneity of cationic potential,which can be realized by constraining the temperature-driven ion diffusion during solid-state reactions.Consequently,P2/O3 biphasic Na_(0.7)Ni_(0.2)Cu_(0.1)Fe_(0.2)Mn_(0.5)O_(2)-δ with well-designed quaternary composition is successfully obtained,exhibiting much-improved rate capabilities(62 mAh g^(-1)at 2.4 A g^(-1)) and cycling stabilities(84%capacity retention after 500 cycles)than its single-phase analogues.Furthermore,synchrotron-based diffraction and X-ray absorption spectroscopy are employed to unravel the underlying sodium-storage mechanism of the P2/O3 biphasic structure.This work presents new insights toward the rational design of advanced layered cathodes for sodium-ion batteries. 展开更多
关键词 Sodium-ion batteries Layered oxides Cationic potential Biphasic structure Cathode materials
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