Thermal insulation materials play an increasingly important role in protecting mechanical parts functioning at high temperatures.In this study,a new porous high-entropy(La_(1/6)Ce_(1/6)Pr_(1/6)Sm_(1/6)Eu_(1/6)Gd_(1/6)...Thermal insulation materials play an increasingly important role in protecting mechanical parts functioning at high temperatures.In this study,a new porous high-entropy(La_(1/6)Ce_(1/6)Pr_(1/6)Sm_(1/6)Eu_(1/6)Gd_(1/6))PO_(4)(HE(6RE_(1/6))PO_(4))ceramics was prepared by combining the high-entropy method with the pore-forming agent method and the effect of different starch contents(0–60vol%)on this ceramic properties was systematically investigated.The results show that the porous HE(6RE_(1/6))PO_(4)ceramics with 60vol%starch exhibit the lowest thermal conductivity of 0.061 W·m^(-1)·K^(-1)at room temperature and good pore structure stability with a linear shrinkage of approximately1.67%.Moreover,the effect of large regular spherical pores(>10μm)on its thermal insulation performance was discussed,and an optimal thermal conductivity prediction model was screened.The superior properties of the prepared porous HE(6RE_(1/6))PO_(4)ceramics allow them to be promising insulation materials in the future.展开更多
Cu_(2)ZnSnS_(4)薄膜因其元素地壳含量丰富、无毒且具有优异的光电性能,受到研究者的广泛关注。本文基于纳米墨水法用Cd部分取代Zn制成了Cu_(2)(Cd x Zn_(1-x))SnS_(4)(CCZTS)薄膜,研究退火时间和后退火温度对薄膜及其太阳电池性能的影...Cu_(2)ZnSnS_(4)薄膜因其元素地壳含量丰富、无毒且具有优异的光电性能,受到研究者的广泛关注。本文基于纳米墨水法用Cd部分取代Zn制成了Cu_(2)(Cd x Zn_(1-x))SnS_(4)(CCZTS)薄膜,研究退火时间和后退火温度对薄膜及其太阳电池性能的影响。研究结果表明,所制备的薄膜为CCZTS相,无其他杂相,薄膜表面平整且致密,结晶性较好。随着退火时间增加,薄膜的晶粒尺寸有所增大,薄膜太阳电池的pn结质量得到提升,其性能也随之提高。通过对薄膜太阳电池进行后退火处理,分析了吸收层的元素扩散对电池性能的影响,在Cd元素形成梯度分布时,电池性能有所提高。随着后退火温度的增加,其电池性能和pn结质量呈现先提高后下降的趋势。经后退火300℃处理后,电池转换效率最佳,为3.13%。展开更多
The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with r...The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with reducing atmosphere (20% H2 and 80% N2). The phase evolution, morphology and afterglow fluorescent properties are systematically studied by the various instruments of XRD, FE-SEM, PLE/PL spectroscopy and fluorescence decay analysis. The PL spectra shows that the Sr1-3xAl2O4:Eu2+x/Dy3+ 2x phosphors display vivid green emission at s519 nm (4f65d1!4f7 transition of Eu2+) with monitoring of the maximum excitation wavelength at s334 nm (8S7=2!6IJ transition of Eu2+), among which the optimal concentration of Eu2+ and Dy3+ is 15 at.% and 30 at.%, respectively. The color coordinates and temperature of Sr1-3xAl2O4:Eu2+ x/Dy3+ 2x phosphors are approximately at (s0.27, s0.57) and s6700 K, respectively. On the above basis, the M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors is obtained by the same method. The PL spectra of these phosphors shows the strongest blue emission at s440 nm and cyan emission at s499 nm under s334 nm wavelength excitation, respectively, which are blue shifted comparing to Sr1??3xAl2O4:Eu2+ x/Dy3+ 2x phosphors. The color coordinates and temperatures of M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors are approximately at (s0.18, s0.09), s2000 K and (s0.18, s0.42), s11600 K, respectively. In this work, long afterglow materials of green, blue and cyan aluminates phosphors with excellent properties have been prepared, in order to obtain wide application in the field of night automatic lighting and display.展开更多
A selective and new spectrophotometric method is described for determination of five 1,4 dihydropyridine drugs (1,4- DHP);namely nifedipine (NIF), nicardipine (NIC), nimodipine (NIM), felodipine (FEL) and amlodipine (...A selective and new spectrophotometric method is described for determination of five 1,4 dihydropyridine drugs (1,4- DHP);namely nifedipine (NIF), nicardipine (NIC), nimodipine (NIM), felodipine (FEL) and amlodipine (AML). The method is based on a coupling reaction between the cited drugs and vanillin reagent in acidic condition. Under optimized conditions, the red coloured products were measured at 500 nm for NIF, NIC, NIM and FEL or at 479 nm for AML. Molar absorptivities were ranged from 0.575 × 104 - 1.065 × 104 l·mol-1·cm-1, Beer’s law was obeyed at 5 - 70 μg/mL concentration range and the limit of detection was ranged from 0.150 - 1.500 μg/mL. The proposed method was successfully extended to pharmaceutical preparations tablets and capsules and comparison by Student’s t-test and variance ratio F-test showed no significant difference.展开更多
Barium metaborate (BaB 2O 4) exists in two forms the high temperature for m α phase and the low temperature form β phase,with the phase transition poi nt at around 925℃.The low temperature phase (β BBO) is an exce...Barium metaborate (BaB 2O 4) exists in two forms the high temperature for m α phase and the low temperature form β phase,with the phase transition poi nt at around 925℃.The low temperature phase (β BBO) is an excellent NLO cryst al for UV region,while the high temperature one (α BBO) is known as a good bir efringent material.α BBO crystal possesses better transparency in the ultravio let region compared with commonly used YVO 4 and CaCO 3 crystals.However,due t o phase transition problem,it is difficult to grow single α BBO crystals by D CZ method,which restricts its wider application.α BBO crystal usually cracks upon cooling resulted from phase transition to β phase.Therefore,it is difficult to grow β BBO single crystals directly from pure BaB 2O 4 mel t;however,to grow single crystals of α BBO is not easy,either. Our recent experiments showed that one could avoid cracking of α BBO cryst als by Sr 2+ doping.This minute amount of Sr 2+ plays the role of structure stabilizer,which inhibits structural reconstruction. In this way,Sr 2+ d op ed BBO single crystals do not subject to phase transition from 925℃ down to roo m temperature. We have mow successfully grown out α BBO single crystals 30mm in diameter by D CZ method from Sr x Ba 1- x BO 4 melt with Sr concentration 0.3 0 .5%.The ratation rate is 10 15r/min,pulling speed is 1 2mm/h.Preliminary tests revealed that its structure and physic chemical properties were almost identic al to those grown from pure melts.These Sr 2+ doped α BBO crystals are no w being widely used in optical isolators.展开更多
基金the National Key R&D Program of China(No.2021YFB3701404)the National Natural Science Fund for Distinguished Young Scholars(No.52025041)+1 种基金the National Natural Science Foundation of China(Nos.52250091,51904021,and 52174294)the Fundamental Research Funds for the Central Universities(Nos.FRF-TP-20-02C2 and FRF-BD-22-05).
文摘Thermal insulation materials play an increasingly important role in protecting mechanical parts functioning at high temperatures.In this study,a new porous high-entropy(La_(1/6)Ce_(1/6)Pr_(1/6)Sm_(1/6)Eu_(1/6)Gd_(1/6))PO_(4)(HE(6RE_(1/6))PO_(4))ceramics was prepared by combining the high-entropy method with the pore-forming agent method and the effect of different starch contents(0–60vol%)on this ceramic properties was systematically investigated.The results show that the porous HE(6RE_(1/6))PO_(4)ceramics with 60vol%starch exhibit the lowest thermal conductivity of 0.061 W·m^(-1)·K^(-1)at room temperature and good pore structure stability with a linear shrinkage of approximately1.67%.Moreover,the effect of large regular spherical pores(>10μm)on its thermal insulation performance was discussed,and an optimal thermal conductivity prediction model was screened.The superior properties of the prepared porous HE(6RE_(1/6))PO_(4)ceramics allow them to be promising insulation materials in the future.
文摘Cu_(2)ZnSnS_(4)薄膜因其元素地壳含量丰富、无毒且具有优异的光电性能,受到研究者的广泛关注。本文基于纳米墨水法用Cd部分取代Zn制成了Cu_(2)(Cd x Zn_(1-x))SnS_(4)(CCZTS)薄膜,研究退火时间和后退火温度对薄膜及其太阳电池性能的影响。研究结果表明,所制备的薄膜为CCZTS相,无其他杂相,薄膜表面平整且致密,结晶性较好。随着退火时间增加,薄膜的晶粒尺寸有所增大,薄膜太阳电池的pn结质量得到提升,其性能也随之提高。通过对薄膜太阳电池进行后退火处理,分析了吸收层的元素扩散对电池性能的影响,在Cd元素形成梯度分布时,电池性能有所提高。随着后退火温度的增加,其电池性能和pn结质量呈现先提高后下降的趋势。经后退火300℃处理后,电池转换效率最佳,为3.13%。
基金the National Natural Science Foundation of China (No. 51602126)the National Key Research and Development Plan of China (No. 2016YFB0303505)+1 种基金China and University of Jinan Postdoctoral Science Foundation (No. 2017M622118 and XBH1716)the 111 Project of International Corporation on Advanced Cement-based Materials (D17001).
文摘The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with reducing atmosphere (20% H2 and 80% N2). The phase evolution, morphology and afterglow fluorescent properties are systematically studied by the various instruments of XRD, FE-SEM, PLE/PL spectroscopy and fluorescence decay analysis. The PL spectra shows that the Sr1-3xAl2O4:Eu2+x/Dy3+ 2x phosphors display vivid green emission at s519 nm (4f65d1!4f7 transition of Eu2+) with monitoring of the maximum excitation wavelength at s334 nm (8S7=2!6IJ transition of Eu2+), among which the optimal concentration of Eu2+ and Dy3+ is 15 at.% and 30 at.%, respectively. The color coordinates and temperature of Sr1-3xAl2O4:Eu2+ x/Dy3+ 2x phosphors are approximately at (s0.27, s0.57) and s6700 K, respectively. On the above basis, the M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors is obtained by the same method. The PL spectra of these phosphors shows the strongest blue emission at s440 nm and cyan emission at s499 nm under s334 nm wavelength excitation, respectively, which are blue shifted comparing to Sr1??3xAl2O4:Eu2+ x/Dy3+ 2x phosphors. The color coordinates and temperatures of M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors are approximately at (s0.18, s0.09), s2000 K and (s0.18, s0.42), s11600 K, respectively. In this work, long afterglow materials of green, blue and cyan aluminates phosphors with excellent properties have been prepared, in order to obtain wide application in the field of night automatic lighting and display.
文摘A selective and new spectrophotometric method is described for determination of five 1,4 dihydropyridine drugs (1,4- DHP);namely nifedipine (NIF), nicardipine (NIC), nimodipine (NIM), felodipine (FEL) and amlodipine (AML). The method is based on a coupling reaction between the cited drugs and vanillin reagent in acidic condition. Under optimized conditions, the red coloured products were measured at 500 nm for NIF, NIC, NIM and FEL or at 479 nm for AML. Molar absorptivities were ranged from 0.575 × 104 - 1.065 × 104 l·mol-1·cm-1, Beer’s law was obeyed at 5 - 70 μg/mL concentration range and the limit of detection was ranged from 0.150 - 1.500 μg/mL. The proposed method was successfully extended to pharmaceutical preparations tablets and capsules and comparison by Student’s t-test and variance ratio F-test showed no significant difference.
文摘Barium metaborate (BaB 2O 4) exists in two forms the high temperature for m α phase and the low temperature form β phase,with the phase transition poi nt at around 925℃.The low temperature phase (β BBO) is an excellent NLO cryst al for UV region,while the high temperature one (α BBO) is known as a good bir efringent material.α BBO crystal possesses better transparency in the ultravio let region compared with commonly used YVO 4 and CaCO 3 crystals.However,due t o phase transition problem,it is difficult to grow single α BBO crystals by D CZ method,which restricts its wider application.α BBO crystal usually cracks upon cooling resulted from phase transition to β phase.Therefore,it is difficult to grow β BBO single crystals directly from pure BaB 2O 4 mel t;however,to grow single crystals of α BBO is not easy,either. Our recent experiments showed that one could avoid cracking of α BBO cryst als by Sr 2+ doping.This minute amount of Sr 2+ plays the role of structure stabilizer,which inhibits structural reconstruction. In this way,Sr 2+ d op ed BBO single crystals do not subject to phase transition from 925℃ down to roo m temperature. We have mow successfully grown out α BBO single crystals 30mm in diameter by D CZ method from Sr x Ba 1- x BO 4 melt with Sr concentration 0.3 0 .5%.The ratation rate is 10 15r/min,pulling speed is 1 2mm/h.Preliminary tests revealed that its structure and physic chemical properties were almost identic al to those grown from pure melts.These Sr 2+ doped α BBO crystals are no w being widely used in optical isolators.
