Degree Of Structural Order Research Articles

High Efficiency n-Type Doping of Organic Semiconductors by Cation Exchange.

Achieving efficient doping in n-type conjugated polymers is crucial for their application in electronic devices. In this study, an n-type doping method is developed based on cation exchange that maintains a high doping level while ensuring a high degree of structural order, leading to significantly improved electrical conductivity. By investigating various dopants and ionic liquids, it is discovered that the choice of dopant influences doping efficiency, while the selection of ionic liquid affects cation exchange efficiency. Through careful selection of suitable dopants and ionic liquids, High doping levels are achieved remarkably in a short period, resulting in the highest conductivity (nearly 1×10- 2Scm-¹) compared to other doping methods for poly{[N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5'-(2,2'-bithiophene)} (N2200). The findings highlight the robustness and efficiency of cation exchange doping as an effective approach for achieving high-quality n-type doping in conjugated polymers, thereby opening new avenues for the development of advanced polymer-based electronic devices.

Synthesis and properties of graphene-like porous carbon from modified cellulose

The work is devoted to the synthesis of graphene-like magnetic nanocomposites by direct pyrolysis of hemp microcrystalline cellulose modified with citric acid containing nickel or cobalt salts. Their chemical structure and morphology were characterized by X-ray diffraction (XRD), electron microscopy (SEM), Raman spectroscopy, low-temperature N2 adsorption-desorption, and Fourier transform infrared spectroscopy (FT-IR). Thermogravimetry has established a possible mechanism of pyrolysis of a modified cellulose matrix containing Ni and Co metals. X-ray diffraction analysis and Raman spectroscopy have shown that an increase in the number of carboxyl groups accelerates the process of graphitization of the cellulose matrix with transition metals (Ni and Co), as well as increases the degree of structural order and the level of graphitization. The conducted studies have shown that nanoparticles of metals of the zero-valence state are enclosed in graphene-like shells having a mainly mesoporous structure.

High-temperature structural drivers immobilizing alkaline substances in red mud-derived mineral wool

Smelting and fiberization of red mud (RM) is an attractive approach for rapid recovery of metal resources, production of mineral wool, and immobilization of hazardous alkalis. However, an enormous challenge remains in understanding alkali immobilization behavior in mineral wool over a broad A/S (Al2O3 to SiO2 mass ratio) range. Here we addressed the challenge through molecular dynamics, thermodynamic and experimental analyses. Increasing A/S ratio caused an increasing degree of structural order and the remarkable micro-phase separation occurred at A/S > 0.9. The role of Na+ and Ca2+ changed from the network-modifying cations to the charge-compensating cations. Melt viscosity decreased and then increased significantly with an intensified temperature sensitivity, identified by the increasing viscous flow activation energy from 211.5 to 377.03 kJ/mol in the temperature region from 1500 to 1570 °C. The transformation of thermodynamic properties (real mixed/excess molar Gibbs free energies, and entropy increment) corresponded to the structural changes. Thermal, mechanical and leaching tests confirmed the negative effect of this structural transformation on alkali immobilization. The A/S ratios controlled below 0.9 were proposed for environmental benefits and product stability. The investigation of immobilization mechanism provides valuable information for tuning the vitrification chemistry and developing safe and green mineral wool from RM.

Carbon Materials With Conductivity Gradients Allow Dynamic Screening of Steep Temperature Differences Along Thin Films

AbstractCarbon materials comprise a wide range of microstructures and excellent electrical and thermal properties while being cost‐effective and readily available. They can be obtained through carbothermal processes at high temperatures, starting from cellulose. Catalytically active compounds, for example, iron salts, strongly influence the carbon microstructure during the graphitization process. Different degrees of structural order can, therefore, be achieved by adjusting the concentration of the iron salts. An infusion withdrawal impregnation approach is used on filter paper to prepare a continuous gradient of the carbon microstructure. This structural change is accompanied by a continuous variation of the closely related electrical and thermal transport properties. Even more, the synergistic interplay of local sheet resistance and thermal diffusivity results in the formation of switchable temperature gradients when an external current is applied. Steady state temperature differences of up to 80 °C are observed along the centimeter‐scaled samples. The controllable temperature gradient formation will be of great interest for applications requiring a fast temperature screening. Furthermore, the temperature gradient can be imposed onto other materials, which will be particularly relevant for advanced thin film characterization applications.

Orientation-dependent multi-spall performance of monocrystalline NiTi alloys under shock compression

The primary objective of this work was committed to large-scale non-equilibrium molecular dynamics modeling for the investigation on multiple spall performance, microstructural evolutions, and melting state of NiTi alloys along three typical crystal orientations. We discovered that there was a single-wave structure present in the [100] orientation, whereas elastic-plastic two-wave structures were found in [110] and [111], exhibiting a significant anisotropy in elastic-plastic wave velocity. Compared to [110] and [111] orientations, multi-spallation was more likely to be generated in the [100] direction. During accumulative dynamic damage, there was also a strong sensitivity of void evolution to orientation. For [100], voids tended to be densely distributed in the material and exhibited a strip-shaped manner. In contrast, a more scattered void distribution was observed for the other two orientations, showing a flaky pattern. Interestingly, dislocations in the spall region were almost annihilated before approaching void nucleation. According to void statistics, the peak number of voids, void nucleation rate, and spall region size were identified to be in a good uniformity along [110], [100], and [111]. For all the cases, the samples experienced partial melting in the released state and were followed by a recovery of structural order degree. However, there was an insignificant anisotropy in the melting state for each crystal orientation during multi-spallation.

Enhancement effect of microwave dielectric properties of Zn3(VO4)2 ceramics based on Cu2+-excited critical melt-state of grains

Here, a low-loss and low sintering temperature Zn3-xCux (VO4)2 (ZCuVO) (x = 0.06) ceramic with two phases has been developed. The addition of Cu2+ induced the Zn3(VO4)2 (ZVO) ceramic to catalyze a small amount of the Zn2V2O7 phase. The macroscopic manifestations of weight loss and heat flow reveal the sintering behavior of ZCuVO ceramics. Final formation and densification of ZCuVO ceramics in the range of 700–825 °C. The addition of trace amounts of Cu2+ promoted the critical melt-state of grains, the improvement of the density, the change of the molecular polarization, and the degree of structural ordering, which ultimately manifested itself in the further enhancement of the microwave dielectric properties. The results show that a moderate amount of Cu2+ substitution can modulate εr, improve the Q×f value, and increase the τf value. The ZCuVO (x = 0.06) ceramic sintered at 775 °C showed excellent performance (εr = 12.62, Q×f = 38798.56 GHz, and τf = −69.29 ppm/°C). This study shows that this ceramic has good potential for LTCC applications and provides a reference for the critical melting state of the grains to enhance microwave dielectric properties.

Symmetry Engineering of Epitaxial Hf0.5Zr0.5O2 Ultrathin Films.

Robust ferroelectricity in HfO2-based ultrathin films has the potential to revolutionize nonvolatile memory applications in nanoscale electronic devices because of their compatibility with the existing Si technology. However, to fully exploit the potential of ferroelectric HfO2-based thin films, it is crucial to develop strategies for the controlled stabilization of various HfO2-based polymorphs in nanoscale heterostructures. This study demonstrates how substrate-orientation-induced anisotropic strain can engineer the crystal symmetry, structural domain morphology, and growth orientation of ultrathin Hf0.5Zr0.5O2 (HZO) films. Epitaxial ultrathin HZO films were grown on the heterostructures of (001)- and (110)-oriented La2/3Sr1/3MnO3/SrTiO3 (LSMO/STO) substrate. Various structural analyses revealed that the (110)-oriented substrate promotes a higher degree of structural order (crystallinity) with improved stability of the (111)-oriented orthorhombic phase (Pca21) of HZO. Conversely, the (001)-oriented substrate not only induces a distorted orthorhombic structure but also facilitates the partial stabilization of nonpolar phases. Electrical measurements revealed robust ferroelectric properties in epitaxial thin films without any wake-up effect, where the well-ordered crystal symmetry stabilized by STO(110) facilitated better ferroelectric characteristics. This study suggests that tuning the epitaxial growth of ferroelectric HZO through substrate orientation can improve the stability of the metastable ferroelectric orthorhombic phase and thereby offer a better understanding of device applications.

10 years of frontiers in carbon-based materials: carbon, the “newest and oldest” material. The story so far

While carbon in itself appears as simple an element as it could possibly get, the undeniable truth is that carbon materials represent a plethora of possibilities both from the perspective of their structure and their applications. While we may believe that carbon is “just another element”, one should never forget that its special ability to coordinate through different hybridizations with apparent ease grants the element properties that no other element may even match. Taking this one step further into the materials realm opens up numerous avenues in terms of materials dimensionality, surface and bulk functionalization, or degree of structural order just to mention a few examples. If these properties are translated into the properties and applications field, the results are just as impressive, with new applications and variants appearing with growingly larger frequency. This has resulted in over a million scientific papers published in the last decade in which the term “carbon” was used either in the title, abstract or keywords. When the search is narrowed down to the field “title” alone, the results drop to just over 318.000 scientific papers. These are figures that no other element in the periodic table can equal, which is a clear indicative that the story of carbon materials is still under constant evolution and development. This review will present an overview of the works published in the Frontiers in Carbon-based materials section during its 10 years of life that reflect the advancements achieved during the last decade in the field of carbon materials.

Effect of horizontal insertion of metal wire mesh into the flame on the formation and suppression of soot in acetylene diffusion flame

A simple and efficient strategy to suppress soot from acetylene diffusion flames is reported for the first time. Horizontally insertion of metal wire mesh into the acetylene diffusion flame is found to greatly suppress the soot emission. The effects of experimental parameters such as acetylene flow rate, wire mesh height above nozzle (WHAN), material of wire mesh, mesh number, and inner diameter of the burner nozzle on soot suppression in acetylene diffusion flames are investigated. In addition, the collected soot samples are characterized by TEM, HRTEM, XRD, BET and Raman. The soot suppression efficiency can reach 100 % by horizontal insertion of the metal wire mesh in the acetylene diffusion flame. The WHAN has a great influence on the effect of soot suppression. In the first 210 s of horizontally inserting the metal wire mesh into the flame, the total mass of collected soot first decreases and then increases with the increase of WHAN. The minimum total mass of soot is achieved when the normalized WHAN (obtained by dividing the wire mesh height above nozzle by flame height without insertion of the wire mesh) is at 0.1. This position corresponds to the soot particle inception zone of the acetylene diffusion flame. The flame is divided into two parts when the metal wire mesh is horizontally inserted into the flame. The temperature of the flame below the metal wire mesh decreases from 1770 K to 1480 K. The temperature of the flame above the metal wire mesh increases from 1590 K to 1780 K. The soot collected on the metal wire mesh grows into a volcano-shaped carbon (VSC) structure. The results of the schlieren imaging experiments show that this structure can promote the mixing of air and fuel in the lower region of the flame thereby suppressing the formation of soot particles. The soot analysis shows that the horizontal insertion of metal wire mesh into the flame leads to high amorphous feature and low degree of structural order of the soot, which means that the oxidation reactivity of the soot increases.

Structural Order-Disorder Analysis of Thermally-Activated Water-Washed Kaolin Particles Using Fourier Transform Infrared Spectroscopy

During the calcination of kaolin particles, kaolinite is thermally activated at high temperatures, causing the crystal structure to collapse and yielding amorphous metakaolinite through dehydroxylation. This metakaolinite is used as a supplementary cementitious material, and one of the most important factors influencing the pozzolanic properties is calcination conditions. Fourier transform infrared spectroscopy (FTIR) has become useful in distinguishing and obtaining information about structural order-disorder and phase transformation following the calcination process. In this study, water-washed kaolin particles were thermally activated at elevated temperatures ranging from 600 to 800 °C for 3–4 h at a rate of 10 °C/min before being analyzed with FTIR to determine the optimum conditions for calcining kaolin particles by examining functional groups, and also to study structural order-disorder or crystallinity of calcined kaolin particles. The most reactive metakaolinite state of water-washed kaolin particles was achieved after 3 h of calcination at 800 °C. Using both empirical and numerical approaches, variations in the position and relative intensity of O-H stretching and deformation of hydroxyl groups in the infrared spectrum can be used to classify the degree of structural order of water-washed kaolin particles. By increasing the calcination temperatures and period, the well-ordered and partially-ordered structures of kaolin particles were transformed into well-ordered, partially-ordered, and poorly-ordered structures. These structural disorder and crystallinity have a significant impact on pozzolanic activity because well-ordered kaolinite can be transformed into less reactive metakaolinite, whereas poorly-ordered kaolinite with high defects can be transformed into more reactive metakaolinite. However, in this study, the structure of water-washed kaolin particles that achieved complete dehydroxylation was discovered to be partially-ordered to poorly-ordered and can be transformed into highly reactive pozzolans.

Accelerated carbonation of regenerated binding material prepared with waste cement paste powder

An approach for the efficient re-utilisation of waste cement paste powders is proposed, wherein the powders are heated to a certain temperature to prepare regenerated binding materials (RBMs), and then rapidly carbonated by high-concentration carbon dioxide to prepare high-strength products. The structural evolution during the heating process of waste cement paste powder and the carbonation process of RBMs were investigated by X-ray diffraction analysis, scanning electron microscopy and 29Si nuclear magnetic resonance spectrum, and the compressive strength of the carbonated RBM samples was measured. The results show that the differences in carbonation reactivity, carbonation products of the RBMs and properties of carbonated RBMs can mainly be attributed to the differences in the degree of structural order of newly formed β-dicalcium silicate (C2S), the content of β-C2S, free calcium oxide (f-CaO) and incompletely decomposed calcium silicate hydrate (C–S–H) in RBMs. The strength of the carbonated sample of RBM prepared at 1050°C was the highest, followed by that prepared at 950°C, which was significantly higher than those prepared at 650, 750 and 850°C. The content of highly ordered β-C2S in RBMs with high carbonation reactivity and the dense stacking of the carbonation products are beneficial for the mechanical properties.

Phase transitions, baro- and piezocaloric effects in single crystal and ceramics of ferroelectric NH4HSeO4

A study of heat capacity, thermal dilatation and sensitivity to hydrostatic and uniaxial pressure was carried out on single-crystal and ceramic samples of NH4HSeO4. The main parameters of low-temperature successive phase transitions B2 (T1) ↔ incommensurate IC (T2) ↔ ferroelectric P1 (T3) ↔ non-ferroelectric did not depend on the type of samples. The behavior of the volumetric strain and the results of direct measurements of T3(p) contributed to the resolution of the longstanding problem associated with the ambiguity of the sign of the corresponding volumetric baric coefficient. The role of thermal expansion anisotropy in the formation of the piezocaloric effect (PCE) near the ferroelectric phase transition at T3 has been studied. Due to the strong difference in the linear baric coefficients, the main contribution to the barocaloric effect (BCE) comes from the inverse intensive and extensive PCE associated with the a-axis. Compared to a single crystal, ceramics demonstrate lower BCE values, which, however, exist in a wider temperature range, which leads to close values of integral caloric parameters. The strong decrease in both BCE and PCE at low-temperature transformations in NH4HSeO4 compared to the ferroelectrics NH4HSO4 and NH4NH4SO4 is associated with a small change in entropy during three low-temperature phase transitions, ΣΔSi = 2.52 J/mol∙K, which is a consequence of a high degree of structural ordering in selenate as a result of a high-temperature transformation at T0 between the superionic and B2 phases, accompanied by a giant change in entropy, ΔS0≈Rln21.

Potential of green-based microporous carbon for advanced water decontamination from azo dyes: Experiment and molecular dynamic simulation studies

Due to severe limitations in clean water resources, there has been an intensified focus on developing cost-effective, remarkably efficient, and recyclable adsorbents to enhance water quality. In this work, a cost-effective biobased activated carbon (AC) adsorbent was synthesized from date palm bark wastes and applied for the removal of two azo dye pollutants sunset yellow (SY), and tartrazine (TZ) from wastewater. The as-prepared powder of activated carbon was fully characterized using different analytical techniques including XRD, FTIR, XPS, Raman spectroscopy, zeta potential, FESEM, pHPZC and N2 adsorption-desorption analysis. These analyses revealed that the resulting biobased AC exhibited a graphene-like layered structure with a noticeable degree of structural order, decorated with diverse surface functional groups. The highly porous structure also demonstrated significant adsorption capacity for SY, and TZ contaminants, particularly at ambient temperatures. It achieved maximum uptakes of approximately 90 mg/g, and 65 mg/g for SY, and TZ respectively, spanning a wide pH range. Moreover, in-depth studies of the adsorption process, including kinetic and thermodynamic analyses, unveiled a chemical, spontaneous, and endothermic sorption mechanism for both SY, and TZ dyes, following a pseudo-second-order model adsorption behavior on the AC structure. Finally, an accurate adsorption mechanism has been proposed for the adsorption of dyes confirmed by experiments and molecular dynamic simulations.

In situ single-droplet analysis of emulsified fat using confocal Raman microscopy: insights into crystal network formation within spatial resolution.

Fat crystallization is one of the predominant factors influencing the structure and properties of fat-containing emulsions. In the present study, the role of emulsifiers on fat crystallization dynamics within droplet multiphase systems was evaluated via single-droplet analysis, taking advantage of the non-destructive properties of confocal Raman microscopy. Palm oil droplets dispersed in water were used as a model system, due to palm oil's well-known crystallization properties. Emulsion droplets of the same size were generated using two different emulsifiers (Whey Protein Isolate and Tween 60), at various concentrations. Fast and slow cooling treatments were applied to affect fat crystallisation and network formation as well as droplet morphology, and crystallization dynamics. Raman imaging analysis demonstrated that the chemical structure and concentration of the emulsifier significantly influenced both crystal nucleation within the droplets, as well as the spatial distribution and morphology of the fat crystal network. Additionally, analysis of the spectra of the crystallized phase provided essential information regarding the impact of the emulsifiers on the microstructure, degree of structural order, and structural arrangements of the fat crystal networks. Furthermore, by performing single droplet analysis during cooling it was possible to observe shape distortions in Tween 60 stabilized droplets, as a consequence of the formation of a three-dimensional network of fat crystals that strongly interacted with the interface. On the other hand, the droplets retained their shape when whey proteins were absorbed at the interface. Confocal Raman microscopy, in combination with polarized light microscopy, is, therefore, a well-suited tool for in situ, single-droplet analysis of emulsified oil systems, providing essential information about emulsified fat crystallization dynamics, contributing to better understanding and designing products with enhanced structure and function.

Mung Bean Starch and Mung Bean Starch Sheet Jelly: NaCl-Based Characteristics Variation.

Empirical evidence indicates that NaCl can improve the quality of mung bean starch sheet jelly (MBSS) when properly incorporated. In this study, by comparison with a sample without NaCl, the influences of NaCl (1.5-8%, w/w) on the physicochemical and structural properties of mung bean starch (MBS) and the quality of MBSS were investigated. MBS with added NaCl had greater gelatinization temperature and pasting parameters but lower gelatinization enthalpy than native MBS. With the addition of NaCl, the drying rate of MBSS first accelerated and then declined in the oven-drying process. The addition of NaCl improved the cooking properties of MBSS but decreased the hardness of cooked MBSS. Rheological results implied that the linear viscoelastic region of cooked MBSS decreased with the NaCl addition, and the storage modulus and tan δ were more frequency-dependent than the loss modulus of cooked MBSS. The addition of NaCl gradually increased the toughness of dried MBSS and the overall acceptability of cooked MBSS. Furthermore, NaCl decreased the structure order degree of starch in MBSS. Correlation analysis demonstrated that the quality of MBSS had a significant correlation with the molecular and lamellar order of starch. Overall, NaCl could improve the quality of MBSS by regulating the thermal, gelatinizing, and structural properties of MBS.

Fine molecular structure and digestibility changes of potato starch irradiated with electron beam and X-ray

The change of digestibility of starch irradiated with different types from the perspective of fine structure is not well understood. In this work, the change of internal structure, molecular weight and chain-length distribution, helical structure, lamellar structure, fractal structure and digestibility of native and treated potato starch with electron beam and X-ray was analyzed. Two irradiations caused the destruction of internal structure, the disappearance of growth rings and increase of pores. Irradiation degraded starch to produce short chains and to decrease molecular weight. Irradiation increased double helical content and the thickness and peak area of lamellar structure, resulting in the reorganization of amylopectin and increase of structure order degree. The protected glycosidic linkages increased starch resistance to hydrolase attack, thereby enhancing the anti-digestibility of irradiated starch. Pearson correlation matrix also verified the above-mentioned results. Moreover, X-ray more increased the anti-digestibility of starch by enhancing ability to change fine structure.

Different graphitization degrees of carbon matter in rocks of a same metamorphic evolution

Two X-ray diffraction methods were chosen to determine the degree of structural order (degree of graphitization) of natural carbonaceous matter. Factors influencing the graphitization processes during the progressive and regressive stages of metamorphism are examined. The correlation of the degrees of structural order of the carbonaceous material with the sequence of mineral growth allows the metamorphic history of the graphite-bearing rocks to be traced. The obtained data can be used for the evaluation of graphite as a raw material.

Shaping the Structure and Properties of TiO2-ZnO Oxide Coatings Produced by Plasma Electrolytic Oxidation on Titanium Substrate.

The paper presents the results of preliminary research on the possibility of synthesizing ZnO-TiO2 mixed coatings by plasma electrochemical oxidation (PEO). The aim of the work was to synthesize TiO2-ZnO mixed coatings on a titanium substrate from an electrolyte containing ZnO nanoparticles (NPs) and to assess the parameters of PEO on the structure, chemical composition, and properties of the obtained oxide coatings. The PEO process was carried out under various current-voltage conditions using different signals: DC, DC pulse, and AC. In this work, optimal conditions for the PEO process were determined to obtain well-adhering oxide coatings with the highest possible content of ZnO. The structure and morphology of the resulting oxide coatings were investigated, and their chemical and phase composition was comprehensively examined (EDX, XRD, XPS, and GD-OES). In addition, their basic optical properties were assessed. It has been shown that in the PEO DC pulse process, it is possible to obtain oxide coatings characterized by a high degree of structure order, high ZnO content in the oxide coating (3.6 at.%, XPS), and prospective applications for photocatalytic purposes (3.12 eV).

Influence of the Change of Phase Composition of (1 - x)ZrO2-xAl2O3 Ceramics on the Resistance to Hydrogen Embrittlement.

The article describes the influence of the change in the phase composition of ceramics on the stability of the crystal structure and retention of thermo-physical parameters during hydrogenation of the surface layer in the proton irradiation process. The selection of irradiation conditions allows modeling the degradation processes of ceramics associated with gas swelling during hydrogenation, as well as revealing the patterns of the effect of phase composition on embrittlement, de-strengthening, and structural degradation resistance. In the course of the conducted studies, dose-dependencies of irradiation-induced structural changes and consecutive accumulation of radiation-induced damage in ceramics as a result of hydrogenation of the damaged near-surface layer were established. It was found that the maximum structural changes are observed at doses above 1015 protons/cm2. Dependencies of the change in the degree of structural order as a function of the dose of accumulated damage and the concentration of accumulated protons were obtained. It was established that the variation of the ceramics phase composition due to the formation of solid solutions of ZrO2/Al2O3 and ZrO2/Al2O3/AlZr3 type leads to an enhancement of resistance to swelling by 3-5 times in comparison with monoclinic ZrO2 ceramics. The general analysis of the variation of strength and thermo-physical parameters of ceramics as a function of irradiation fluence for ceramics with different phase compositions showed a direct dependence of the decrease in hardness, resistance to cracking, and thermal conductivity on the concentration of deformation structural distortions caused by irradiation.

Evaluation of the Applicability of Modifying CdSe Thin Films by the Addition of Cobalt and Nickel to Enhance the Efficiency of Photocatalytic Decomposition of Organic Dyes

This article presents the results of an assessment of the use of CdSe, NiCdSe, and CoCdSe thin films as a basis for photocatalysts used for the decomposition of the organic dyes rhodamine B, cargo red, and indigo carmine. Interest in this area was determined by the need to solve a number of issues related to increasing the efficiency purifying aqueous media from the negative effects of organic dyes, which cannot be disposed of using traditional methods associated with adsorption or filtration. The use of the electrochemical synthesis method to obtain thin films of a given thickness showed that the addition of nickel or cobalt sulfates to the standard electrolyte solution used to obtain CdSe films results in the formation of CdSe films with a higher degree of structural ordering (the crystallinity degree was more than 50%), as well as a decline in the band gap. When analyzing data on the photocatalytic decomposition of organic dyes, it was found that a change in the structure of the films due to the introduction of nickel and cobalt leads, in the case of the decomposition of the rhodamine B dye, to a more efficient decomposition, and in the case of the cargo red and indigo carmine dyes, not only to their complete decomposition and mineralization, but also to a reduction in the time of photocatalytic reactions (decomposition growth rate). Moreover, an analysis of cyclic tests demonstrated that NiCdSe and CoCdSe films maintain 90% of their photocatalytic decomposition efficiency compared to that achieved during the first decomposition cycle, while CdSe degrades after three consecutive cycles and its efficiency reduces by more than 2.5–3 times.