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The world's perennial need for energy and microelectronic miniaturization brings with it a broad set of technological and scientific challenges. Materials characterized by precise microstructural architectures based on fractal analysis and ranging in size down to nano scale represent an important avenue for finding novel solutions. Deep materials structure hierarchies of this type open new possibilities in capacity according to the Heywang model, especially when extended by a fractals approach and intergranular relationships supported and recognized by their fractal nature. These developments are opening new frontiers in microelectronics miniaturization. They build on early fractal applications that were used as tools in miniaturization research and also provided application perspectives for diverse energy technologies. In other words, fractals, as a crucial concept of modern theoretical-experimental physics and materials sciences, are tightly linked to higher integration processes and microelectronics miniaturization. They also hold potential for meeting the energy exploitation challenge. In this research context, for the first time we experimentally and theoretically investigated the electrostatic field between the grains within fractal nature aspects. It is essentially a theoretical experiment based on samples of experimental microstructures imaged with SEM, as previously published in a number of other papers. We now take the research a step further by consolidating the experimental samples with respect to the predicted distribution of grains and pores within the sample mass. We make an original contribution by opening the frame of scale sizes with respect to the technical processes of consolidation. This lets us predict the constitutive elements of the microstructures – approximately equidistant grains and pores. In this paper we define in a practical manner the final target elements for experimental consolidation of real samples. It is the main bridge between a

The world's perennial need for energy and microelectronic miniaturization brings with it a broad set of technological and scientific challenges. Materials characterized by precise microstructural architectures based on fractal analysis and ranging in size down to nano scale represent an important avenue for finding novel solutions. Deep materials structure hierarchies of this type open new possibilities in capacity according to the Heywang model, especially when extended by a fractals approach and intergranular relationships supported and recognized by their fractal nature. These developments are opening new frontiers in microelectronics miniaturization. They build on early fractal applications that were used as tools in miniaturization research and also provided application perspectives for diverse energy technologies. In other words, fractals, as a crucial concept of modern theoretical-experimental physics and materials sciences, are tightly linked to higher integration processes and microelectronics miniaturization. They also hold potential for meeting the energy exploitation challenge. In this research context, for the first time we experimentally and theoretically investigated the electrostatic field between the grains within fractal nature aspects. It is essentially a theoretical experiment based on samples of experimental microstructures imaged with SEM, as previously published in a number of other papers. We now take the research a step further by consolidating the experimental samples with respect to the predicted distribution of grains and pores within the sample mass. We make an original contribution by opening the frame of scale sizes with respect to the technical processes of consolidation. This lets us predict the constitutive elements of the microstructures – approximately equidistant grains and pores. In this paper we define in a practical manner the final target elements for experimental consolidation of real samples. It is the main bridge between a

The world's perennial need for energy and microelectronic miniaturization brings with it a broad set of technological and scientific challenges. Materials characterized by precise microstructural architectures based on fractal analysis and ranging in size down to nano scale represent an important avenue for finding novel solutions. Deep materials structure hierarchies of this type open new possibilities in capacity according to the Heywang model, especially when extended by a fractals approach and intergranular relationships supported and recognized by their fractal nature. These developments are opening new frontiers in microelectronics miniaturization. They build on early fractal applications that were used as tools in miniaturization research and also provided application perspectives for diverse energy technologies. In other words, fractals, as a crucial concept of modern theoretical-experimental physics and materials sciences, are tightly linked to higher integration processes and microelectronics miniaturization. They also hold potential for meeting the energy exploitation challenge. In this research context, for the first time we experimentally and theoretically investigated the electrostatic field between the grains within fractal nature aspects. It is essentially a theoretical experiment based on samples of experimental microstructures imaged with SEM, as previously published in a number of other papers. We now take the research a step further by consolidating the experimental samples with respect to the predicted distribution of grains and pores within the sample mass. We make an original contribution by opening the frame of scale sizes with respect to the technical processes of consolidation. This lets us predict the constitutive elements of the microstructures – approximately equidistant grains and pores. In this paper we define in a practical manner the final target elements for experimental consolidation of real samples. It is the main bridge between a

Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.

Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.

Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.

Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.

Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.

A new approach, based on fractal geometry and correlation between microstructure-nanostructure and rare-earth properties and other additives doped BaTiO3-ceramics and electronics properties, is applied. The grain contacts geometry based on different stereological models and especially intergranular contact surface fractal morphology was the subject of several papers of these authors. The main conclusion was that intergranular capacities have higher values then expected which is induced by contact surfaces sizes augmentation as a consequence of their fractal nature. Bigger micro-capacities were justified by virtually having bigger dielectric constants which was achieved by introducing fractal correction factor α0>1, as a multiplier to the usual dielectric constant εr to gain a bigger value of α0εr. In further BaTiO3-ceramics micro-electronics fractal theory development, different fractal methods were used to describe complexity of the spatial distribution of BaTiO3-grains, as well as pores. This led to a fractal correction factor revisited model, which considers existence of surfaces fractality, pores fractality and the inner liquid dynamics and solid state sintering phase within ceramics material represented by the Brownian motion model. The new correction factor α is a function of these three ceramics fractality "sources". Here, the relationship between α and α0 is established for doped BaTiO3-ceramics using the Curie-Weiss law and temperature as an omnipresent sintering parameter. Also, the model of two grains contact impedance is studied for different α and frequency values. By the control of shapes and contact surfaces numbers on the entire BaTiO3-ceramic sample level, the control over structural properties of these ceramics can be achieved, with the aim of correlation between material electronic properties and corresponding microstructure. The fractal nature for analysis of the ceramics structure provides a new approach for modeling and prognosis of the grai

A new technology for radionuclide trapping which is based on bio-templating approach was proposed in this paper. Porous oxide ceramics was prepared by wet impregnation of biological template with water solution of cerium and strontium nitrates. The template was derived from linden wood (tilia amurensis). Repeated pressure impregnation, heat treatments and final calcination at 1000 °C in air resulted in the template burnout and consolidation of the oxide layers. The obtained products had structure which corresponded to the negative replication of biological templates. X-ray diffraction, scanning electron microscopy, Raman spectroscopy and porosimetry were employed to characterize the composition and structure of biomorphic ceramics. It was found that the wood impregnated with water solution of cerium and strontium nitrates was converted into oxide ceramics (Ce0.9Sr0.1O2−δ), while preserving the microstructural features of the biological preform.

The structure of BaTiO3 based materials can be controlled by using different technological parameters and different additives. In this paper, microstructure and dielectrical properties of Er2O3 doped BaTiO3-ceramics, sintered from 1320 °C to 1380 °C have been investigated. Microstructural investigations were carried out using scanning electron microscope equipped with energy dispersive spectrometer. Grain size distribution was determined by quantitative metallography method. The new correlation between microstructure and dielectric properties of doped BaTiO3-ceramics, based on fractal geometry and contact surface probability, has been developed. Using the fractals and statistics of the grains contact surface, a reconstruction of microstructure configurations, as grains shapes or intergranular contacts, has been successfully done. Obtained results indicated that fractal analysis and statistics model for contact surfaces of different shapes were very important for the prognosis of BaTiO3-ceramics microstructure and dielectric properties. The morphology of ceramics grains pointed out the validity of developing new structure analytical methods, based on different grains’ shape geometries. The grains contact model based on ellipsoidal geometry is presented as new modeling tool for structure research of BaTiO3-ceramics materials. The directions of possible materials properties prognosis are determined according to the correlations synthesis–structure–property.The statistical approach to the investigation of BaTiO3-ceramic grains concerning the relationship between the temperature and the area of the contact surface is also introduced.

The structure of BaTiO3 based materials can be controlled by using different technological parameters and different additives. In this paper, microstructure and dielectrical properties of Er2O3 doped BaTiO3-ceramics, sintered from 1320 °C to 1380 °C have been investigated. Microstructural investigations were carried out using scanning electron microscope equipped with energy dispersive spectrometer. Grain size distribution was determined by quantitative metallography method. The new correlation between microstructure and dielectric properties of doped BaTiO3-ceramics, based on fractal geometry and contact surface probability, has been developed. Using the fractals and statistics of the grains contact surface, a reconstruction of microstructure configurations, as grains shapes or intergranular contacts, has been successfully done. Obtained results indicated that fractal analysis and statistics model for contact surfaces of different shapes were very important for the prognosis of BaTiO3-ceramics microstructure and dielectric properties. The morphology of ceramics grains pointed out the validity of developing new structure analytical methods, based on different grains’ shape geometries. The grains contact model based on ellipsoidal geometry is presented as new modeling tool for structure research of BaTiO3-ceramics materials. The directions of possible materials properties prognosis are determined according to the correlations synthesis–structure–property.The statistical approach to the investigation of BaTiO3-ceramic grains concerning the relationship between the temperature and the area of the contact surface is also introduced.