Crystal Phase Research Articles

Azobenzene derivatives with two aliphatic chains: mesogenic and photoisomerisation studies of (E)-4-[(4-heptyloxyphenyl)diazenyl]phenyl alkanoates (7OABOOCm)

ABSTRACT Compounds from the homologous series of (E)-4-[(4-heptyloxyphenyl)diazenyl]phenyl alkanoates (7OABOOCm) for m = 1–19, were synthesised. The phase behaviour was investigated by differential scanning calorimetry, polarised light (optical) microscopy, and thermo-optical analysis. The enantiotropic nematic, smectic C and crystal G phases were found for derivatives with m = 1–18, m = 7–17, and m = 4, respectively. In addition, during cooling, smectic F, crystal G, and unknown X phases were observed for derivatives with m = 7–9, m = 3,8,9, and m = 4, respectively. The X-ray diffraction results suggest that the X phase is presumably monotropic crystal H or a second crystal phase. The E–Z photoisomerisation process was observed during UV light irradiation. A photostationary state was reached after exposure time equal to approximately 80 s. The derived kinetic constant k of this process was of the order of 10−2 s−1.

Thermotropic "Plumber's Nightmare" - A Tight Liquid Organic Double Framework.

Gyroid, double diamond and the body-centred "Plumber's nightmare" are the three most common bicontinuous cubic phases in lyotropic liquid crystals and block copolymers. While the first two are also present in solvent-free thermotropics, the latter had never been found. Containing six-fold junctions, it was unlikely to form in the more common phases with rod-like cores normal to the network columns, where a maximum of four branches can join at a junction. The solution has therefore been sought in side-branched mesogens that lie in axial bundles joined at their ends by flexible "hinges". But for the tightly packed double framework, geometric models predicted that the side-chains should be very short. The true Plumber's nightmare reported here, using fluorescent dithienofluorenone rod-like mesogen, has been achieved with, indeed, no side chains at all, but with 6 flexible end-chains. Such molecules normally form columnar phases, but the key to converting a complex helical column-forming mesogen into a framework-forming one was the addition of just one methyl group to each pendant chain. A geometry-based explanation is given.

Rapid Joule heating fabrication of Ru cluster-loaded WO3 on carbon nanotubes to enhance alkaline electrocatalytic hydrogen production activity

The design of efficient electrocatalysts for hydrogen evolution reaction (HER) suitable for industrial applications remains a challenging task. In this work, Ru clusters were loaded onto WO3 which were grown on carbon nanotubes (WRu/C-JH) using a rapid Joule heating method. The crystal phases of WO3 was transformed, and abundant active sites were exposed during the rapid heating and cooling process. All these modifications contributed to the greatly improved electrocatalytic activity in HER. As tested, in 1 M KOH, it only required an overpotential of 22 mV to reach 10 mA cm−2 and 401 mV to reach a high current density of 1 A cm−2 on WRu/C-JH. Moreover, WRu/C-JH demonstrated excellent stability at 500 mA cm−2 for 100 h. Furthermore, a two-electrode system was constructed to assess overall water splitting performance of WRu/C-JH. This system was capable of reaching 100 mA cm−2 at a low voltage of 1.94 V. The mechanism of the enhancement in HER for as-prepared sample was also deeply discussed.

Preparation and antibacterial evaluation of silver-doped zirconia for enhanced dental restoration performance.

Because of its superior strength, esthetic properties, and excellent biocompatibility, zirconia is preferred for dental prosthetic such as crowns and bridges. However, zirconia crowns and bridges are susceptible to secondary caries owing to margin leakage. Silver is a well-known antibacterial agent, making it a desirable additive to zirconia crowns and bridges for secondary caries prevention. This study focuses on imparting zirconia composite with antibacterial properties to enhance its protective capacity in dental restorations. We used the sol-gel method to dope Ag into zirconia. Silver-doped zirconia powders were prepared at Zr:Ag molar ratios of 100:0,100:0.1, 100:0.5, 100:1, 100:3, and 100:5 (respective samples denoted as Ag-0, Ag-0.1, Ag-0.5, Ag-1, Ag-3, and Ag-5) and were subjected to firing at various temperatures (400-1,000 °C). We performed X-ray diffraction to investigate the crystal phase of these powders and X-ray fluorescence and field emission scanning electron microscopy to analyze their elemental composition and surface morphology, respectively. Moreover, we performed spectrophotometry to determine the L*a*b* color values, conducted dissolution tests, and quantified the Ag content through inductively coupled plasma optical emission spectroscopy (ICP-OES). In addition, we studied the antibacterial activity of the samples. Analyses of the samples fired at ≤600 °C revealed a predominantly white to grayish-white coloration and a tetragonal crystal phase. Firing at ≥700 °C resulted in gray or dark gray coloration and a monoclinic crystal phase. The Ag content decreased after firing at 900 °C or 1,000 °C. Ag-0.5 and above exhibited antibacterial activity against both Escherichia coli and Staphylococcus aureus. Therefore, the minimum effective silver-doped zirconia sample was found to be Ag-0.5. This study allows the exploration of the antimicrobial potential of silver-doped zirconia materials in dental applications such as prosthdontical lining materials, promoting the development of innovative restorations with protective capacity against secondary caries.&#xD.

Biochar assisted synthesis of α-MnO2 nanowires with superior performance for non-radical activation of peroxymonosulfate

Non-radical activation of peroxymonosulfate (PMS) is a promising water treatment technology for removing refractory organics, but its mechanism is still ambiguous and the development of highly efficient catalyst is still a challenge. Herein, α-MnO2 nanowires were synthesized by a hydrothermal method with the assistance of biochar and their performance for PMS activation was studied. The characterization results show that the addition of biochar had little effect on the crystal phase and valence state of MnO2 but significantly reduced the size of nanowires. These nanowires had mesoporous structure, high surface area and oxidation ability, resulting in their superior performance for removing organic pollutants with PMS activation. The degradation of phenol by α-MnO2-PMS followed first order kinetics with an activation energy of 14.82 kJ mol−1. Electron paramagnetic resonance and radical scavenging experiments demonstrated that this activation process followed the non-radical mechanism. The quenching effect of scavengers led to the misleading role of singlet oxygen. In fact, surface activated PMS (MnO2–PMS*) rather than singlet oxygen was the reactive species. Weak acidic condition was conducive for the formation of MnO2–PMS* complexes. This catalyst exhibited good reusability and high activity for removing various organic pollutants, and the common substances in real water had little effect on its performance, suggesting its potential application in wastewater treatment.

Purification and investigation of tellurium rich Te-As-Se chalcogenide glass for extended far-infrared transmission

In the present study, tellurium-rich (45–55 mol%) As-Se-Te chalcogenide glasses were synthesized and purified further to eliminate the impurities for achieving extended far infrared transmission. The glasses were characterized and studied for physical, thermal, optical, structural and mechanical properties. All the glasses have shown transparency in the wavelength range of ∼1.6–19 µm, with >45 % transmission with impurities. The purification process through vacuum distillation has eliminated the oxide impurities in the glass and the glass displayed ∼52 %T in the wide infrared region. The refractive index for purified glass decreased from 3.487 at 2 µm to 3.362 at 10 µm. The purified glass was heat treated for four hours, and the most dominant crystal phase, As2Te3 was observed in XRD analysis. Presence of sharp Raman peak at ∼120 cm−1 belonging to As2Te3 pyramids in heat-treated sample well agreed with the XRD results.

The Effects of Electric Fields on Protein Phase Behavior and Protein Crystallization Kinetics.

We experimentally studied the effects of an externally applied electric field on protein crystallization and liquid-liquid phase separation (LLPS) and its crystallization kinetics. For a surprisingly weak alternating current (AC) electric field, crystallization was found to occur in a wider region of the phase diagram, while nucleation induction times were reduced, and crystal growth rates were enhanced. LLPS on the contrary was suppressed, which diminishes the tendency for a two-step crystallization scenario. The effect of the electric field is ascribed to a change in the protein-protein interaction potential.

Preparation of low thermal expansion, transparent LAS glass-ceramics via simplified heat-treatment method

Li2O-Al2O3-SiO2 (LAS) glass-ceramics are commercially significant due to their unique microstructure and exceptional properties, including near-zero thermal expansion coefficient, making them suitable for a wide range of applications. However, the content of SiO2 and Al2O3 in the composition of LAS glass is very high, which leads to high viscosity and very difficult melting of this type of glasses. In order to reduce the melting temperature of the glass, use of relatively high Na2O in the basic glass composition allows high-quality glass to melt. Employing a simplified heat-treatment method, LAS glass-ceramics are prepared with Australian spodumene as the primary material. By exploring the effect of crystallization temperature on the structures and properties of the resulting LAS glass-ceramics, samples with excellent comprehensive properties are achieved. The prepared glass-ceramics are thoroughly characterized using DSC, XRD, FTIR, SEM, and TEM, along with assessments of their viscosity, thermal, optical, and mechanical properties. Relatively more Na2O is introduced into the glass compositions, which can lower the melting temperature of the glass to below 1600 oC. The basic glass is annealed at 700 oC for 2 h, nucleation phenomenon Nucleation phenomenon can be generated in the LAS glasses. When the microcrystalline temperature of glasses increases from 835 oC to 910 oC, the main crystalline phase of glass-ceramics changes from β-quartz solid solution to β-spodumene solid solution. The change in the main crystal phase has significantly affected the properties of glass-ceramics. When the crystallization temperature is below 860 °C, the glass-ceramics exhibit a low negative expansion coefficient (<-0.5×10-6 K-1), high visible light transmittance (>85%), and excellent average flexural strength (173.3 MPa).

Solution-Processed Pb(Zr,Ti)O3 Thin Films with Strong Remnant Pockels Coefficient.

In contrast to the widely studied electrical properties of Pb(Zr,Ti)O3 thin films, which have led to their applicability in various application areas such as thin film capacitors, microelectronics, and ferroelectric memories, the electro-optic (EO) properties are far less studied, which hinders the applicability of Pb(Zr,Ti)O3 films for EO applications such as heterogeneously integrated phase modulators in silicon (Si) photonics. Therefore, the EO properties of Pb(Zr,Ti)O3 films need to be further investigated to pave the way for the applicability of Pb(Zr,Ti)O3 films in EO applications. As the EO properties of ferroelectric thin films strongly depend on their crystal phase and texture, which in turn are influenced by the method of film fabrication. Therefore, in this work, we investigate the EO properties of a promising solution process using a La2O2CO3 template film. We successively characterize the precursor ink, microstructure and EO properties of the solution-processed Pb(Zr,Ti)O3film. The Pb(Zr,Ti)O3 film exhibits a fiber texture and has a large maximum and remnant Pockels coefficient (reff) of 69 pm V-1 and 66 pm V-1, respectively. The integration into a ring resonator-based modulator shows a VπL of 2.019 V cm. The determination of these promising EO properties could further pave the way for the applicability of Pb(Zr,Ti)O3 thin films in Si photonics.

Bilateral Embedded Anchoring via Tailored Polymer Brush for Large-Area Air-processed Blue Light-Emitting Diodes.

Perovskite light-emitting diodes (PeLEDs) that can be air-processed promises the development of displaying optoelectronic device, while is challenged by technical difficulty on both the active layer and hole transport layer (HTL) caused by the unavoidable humidity interference. Here, we propose and validate that, planting the polymer brush with tailored functional groups in inorganic HTL, provides unique bilateral embedded anchoring that is capable of simultaneously addressing the n phases crystallization rates in the active layer as well as the deteriorated particulate surface defects in HTL. Exemplified by zwitterionic polyethyleneimine-sulfonate (PEIS) in present study, its implanting in NiOx HTL offers abundant nuclei sites of amino and sulfonate groups that balance the growth rate of different n phases in quasi-2D perovskite films. Moreover, the PEIS effectively nailed the interfacial contact between perovskite and NiOx, and reduced the particulate surface defects in HTL, leading to the enhanced PLQY and stability of large-area blue perovskite film in ambient air. By virtue of these merits, present work achieves the first demonstration of the air-processed blue PeLEDs in large emitting area of 1.0 cm2 with peak external quantum efficiency (EQE) of 2.09 %, which is comparable to the similar pure-bromide blue PeLEDs fabricated in glovebox.

Study on the effect of heat treatment on the structure, mechanical and electrical properties of alumina fiber insulation

In this paper, the heat treatment of alumina fiber was studied. The infiltration agent on the fiber surface was removed after heat treatment at 450 °C for 6 h. TG-DSC, scanning electron microscope, x-ray diffraction, Fourier infrared spectrometer, energy dispersive spectrometer, and patterning were used to analyze the thermal weight loss, fiber surface morphology, crystal structure, and composition of alumina fibers. The results show that the aluminum oxide fiber has excellent temperature resistance and does not undergo crystal phase transformation during thermal weight loss. After heat treatment, the fiber surface infiltration agent ablates and dissolves from the fiber surface, and the internal crystal structure of the fiber remains stable. The tensile testing machine was utilized to test the breaking strength of alumina fiber. The fiber still maintained high strength after heat treatment, and the retention rate of breaking strength was greater than 74%. ZC-90G high insulation resistance measuring instrument and WDY-Ⅱ automatic voltage tester were utilized to analyze the insulation resistivity and breakdown strength of alumina fiber before and after heat treatment. The results show that heat treatment can effectively improve the insulation performance and breakdown strength of alumina fiber.

A General Nucleation Model for Semiconductor Nanocrystals.

We introduce a nonclassical model for nanocrystal nucleation in solution which centers on the dynamic interplay of chemical bond breakage and formation coupled with the desolvation of precursor molecules, which we term the molecular chemistry (MC) model. Departing from classical theory, our model employs the bond count as the key variable rather than particle size, thereby redefining the role of supersaturation and its role in determining the so-called critical nucleus size. We apply the model to CdSe nanocrystal formation in nonpolar solvents and showcase its efficacy in predicting solvent dynamics, precursor characteristics, crystal phase, stoichiometry, "magic number" behavior, and transition states. While the coupled-cluster method is used to determine the bond energy, we show that it is possible to derive reaction pathways by reducing the calculations to algebraic approximations for the nucleation energy. This singular set of bond energy parameters allows nanocrystal nucleation and growth to be conceptualized as a straightforward chemical reaction.

Synthesis of nitrogen-doped crystalline Ga2O3 thin films via trimethylgallium doped NH3/H2/N2/O2 premixed stagnation flames

This study presents a novel and cost-effective technique for fabricating nitrogen-doped crystalline α-Ga2O3 and β-Ga2O3 thin films under atmospheric pressure conditions through flame synthesis for the first time. We employ metal–organic ammonia (NH3)-assisted flame synthesis (MO-NAFS) in a quasi-one-dimensional trimethylgallium (TMG) doped NH3/H2/N2/O2 flat flame to achieve a one-step deposition of Ga2O3 onto c-plane α-Al2O3 substrates. We found that hydrogen (H2) addition directly impacts the crystallinity of the Ga2O3 thin film. When only NH3 is employed as the fuel, a thin-film single-crystal nitrogen-doped β-Ga2O3 was observed. Blending the NH3 with 5 % of H2 yields a single-crystal nitrogen-doped α-Ga2O3, while a further increase of H2 fraction up to 10 % results in a mixture of both α-Ga2O3 and β-Ga2O3 crystals. Remarkably, the nitrogen doping through MO-NAFS was found to persistently result in an N/O atomic ratio as high as 1.12, as determined by the XPS analysis. This approach paves the way to a simple and scalable means for producing crystalline nitrogen-doped Ga2O3 thin films with potential control of crystal phase composition through parameter adjustments.

Synthesis of CoMnFe2O4 hollow microstructure decorated GO for photocatalytic degradation of organic dyes

Over the past decade, safeguarding marine life and aquatic ecosystems against deleterious dye pollutants has emerged as a paramount concern. Methylene blue dye stands out as one such pollutant capable of inflicting irreversible damage to marine ecosystems even at minute concentrations. Addressing this pressing issue, we synthesized a novel CoMnFe2O4/graphene oxide nanocomposite employing a microwave-ultrasonic method. This composite, comprising soft superparamagnetic CoMnFe2O4 hollow microstructures integrated onto graphene oxide surfaces, revealed a mesoporous structure with a notably high surface area, which was about 96.4654 m2.g−1. Various analytical techniques were employed to scrutinize the crystal structure, functional groups, surface chemical composition, and morphologies of the synthesized CoMnFe2O4/graphene oxide nanocomposite (X-ray diffraction, Fourier-Transform Infrared Spectroscopy, energy-dispersive X-ray spectroscopy, field emission scanning electron microscopy, and high-resolution transmission electron microscopy). The CoMnFe2O4 crystal phase appears to be cubic in the X-ray diffraction with a 28.91 nm Avg. crystallite size. The measured band gap energies for the CoMnFe2O4, graphene oxide, and CoMnFe2O4/graphene oxide nanocomposite are 2.23 eV, 2.90 eV, and 1.89 eV, respectively. Remarkably, under visible light irradiation, the nanocomposite exhibited an impressive degradation efficiency of 97.54 % within just fifty minutes (at pH = 7, Methylene blue conc. = 15 mg/L, and catalyst dose = 0.05 g.), attributed to a photo degradation rate constant (k value) reaching 0.07330 min−1. Notably, this efficiency nearly doubled with the introduction of H2O2 peroxide. The outstanding recyclability of the CoMnFe2O4/graphene oxide nanocomposite, sustaining optimal performance over four cycles without significant degradation, underscores its potential for long-term environmental remediation efforts. Moreover, its magnetic extractability from contaminated solutions enhances its suitability for advanced environmental applications.

Orientational transitions of discotic columnar liquid crystals in cylindrical pores.

Confined in a cylindrical pore with homeotropic anchoring condition, the hexagonal columnar phase of discotic liquid crystals can form a "log-pile" configuration, in which the columns are perpendicular to the long axis of the pore. However, the {100} planes of the hexagonal lattice can orient either parallel (termed (100)‖ orientation) or perpendicular ((100)⊥) to pore axis. Here we experimentally show that the (100)‖ orientation is found in narrower cylindrical pores, and the (100)‖-(100)⊥ transition can be controlled by engineering the structure of the molecules. The (100)‖ orientation is destroyed in asymmetric discotics hepta(heptenyloxy)triphenylene (SATO7); replacing the oxygen linkage in hexa(hexyloxy)triphenylene (HATO6) by sulphur (HATS6) improves the (100)‖ orientation in small pores; adding a perfluorooctyl end to each alkyl chain of HATO6 (HATO6F8) moves the (100)‖-(100)⊥ transition to larger pores. We have provided a semi-quantitative explanation of the experimental observations, and discussed them in the context of previous findings on related materials in a wider pore size range from 60 nm to 100 μm. This allows us to produce a comprehensive picture of confined columnar liquid crystals whose applications critically depend on our ability to align them.

Microstructural analysis and densification of ordinary Portland cement mortars incorporated with minimal nano-TiO2: intermixing and surface coating on both fresh and hardened surfaces

The present study investigated the microstructural properties of ordinary Portland cement (OPC)-modified with minimum dosage of nano TiO2 on fresh and hardened cement mortar surfaces and intermixed samples. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX) were used to analyze the morphology and hydration products of the OPC specimens doped with nanotitanium (NT).Additionally, XRD coupled with Rietveld refinement was employed to quantify the crystal phases and refine the crystal structure model through the comparison of the calculated diffraction pattern to the measured pattern. Subsequently, crystallographic analysis was conducted to evaluate the crystallographic structure and to confirm the existence of specific atoms and bonds within the crystal structure altered with NT. The findings revealed that the addition of minimal NT resulted in a more compact and denser microstructure, characterized by increased formation of calcium silicate hydrate (CSH) gel and a reduction in calcium hydroxide (CH) crystals.This led to a reduction in the porosity of the hardened coating surface, with similar improvements observed for the fresh coating and intermixed samples compared to those of the control mortar. A decrease in the lattice parameters, accompanied by an increase in the number of atoms, bonds and polyhedra in the crystal structure, led to alterations in the interatomic spacing and contributed to the densification of the cementitious matrix.The findings also showed that NT integration led to a more compact structure with shorter bond distances and smaller polyhedral volumes for the Ti samples than for the control sample. Moreover, compared with the freshly cast and hardened coating samples, the NT-intermixed samples exhibited the shortest Ti–O bond distances and the smallest polyhedral volume. Overall, the analysis presented in this study significantly contributes to the development of novel and environmentally friendly photocatalytic cementitious materials at minimal dosages.

Enhanced intrinsic thermal conductivity of liquid crystalline polyester dispersed films through hydrogen bond interaction

Polymer-dispersed liquid crystal (MHxFy) films comprising liquid crystal polymer (LCPH and LCPF) were successfully obtained by the method of solution casting & thermal compressing. At a LCPH mass fraction of 67%, thermal conductivity (λ) value in through-plane (λ⊥) and in-plane (λ∥) direction of MH2F1 films reach up to 0.305 W/(m·K) and 2.879 W/(m·K), respectively. In comparison to pure LCPF, the thermal conductivity of MH2F1 exhibited an increase of 4.42 times, which is 14.4 times than that of conventional thermoplastics. Meanwhile, the crystallinity of MHxFy films around 50% which is indicate the crystal phase become more integrated and regular. The FTIR spectra reveals a significant blue shift (3432 cm−1 to 3421 cm−1) in the absorption peak of the −OH group in MH2F1, suggesting a robust interaction between LCPF and LCPH. The primary cause of elevated thermal conduction in these films was determined to be the consistent presence of “thermal bridges” and a high degree of crystallinity. Furthermore, the T5%, Tmax and residual carbon at 800 °C of MH2F1 were 347.8 °C, 409.4 °C and 8%, respectively. This is attributed to the ordered distribution of LCPH in LCPF matrix through hydrogen bonding interaction, forming an interpenetrating network of LCPF-LCPH. The result show that MHxFy films demonstrating superior intrinsic thermal conductivities, thermal stabilities, and mechanical properties.

Influence of high field strength ions on the crystallization characteristics and properties of slag glass-ceramics

Blast furnace slag glass–ceramics were prepared by melting using rare-earth-containing blast furnace slag (REBFS) as the main raw material and Fe2O3 and Cr2O3 as composite nucleating agents. By adding different TiO2 contents, the study comprehensively revealed the effects of high field strength ions on the glass network structure, crystalline properties, elemental distribution and physicochemical properties. Raman spectroscopy and differential scanning calorimetry revealed that TiO2 acted primarily as a network modifier in the glass network. The appropriate TiO2 content disrupted the glass network, decreasing the crystallization activation energy (EC) of the glass–ceramic. However, excess TiO2 repaired the network structure, thereby increasing the EC. The combined effect of the Cr and Ti substantially improved the crystallization characteristics of the glass-ceramics. Cr2O3 induced the formation of spinel, which promoted the crystallization of the main crystalline augite phase. The self-aggregation of the high field strength Ti4+ ion induced the formation of a titanium- and cerium- containing titanite phase, which also contributed to grain refinement. This titanite phase effectively increased the Vickers hardness and acid and alkali resistances of the glass-ceramics to 9.16GPa and over 98.5%, respectively. The excellent physicochemical properties render REBFS glass–ceramics as being promising materials for various construction applications. This research provides theoretical support for comprehensively utilizing blast furnace slag and provides theoretical guidance for preparing slag glass–ceramics possessing desirable physicochemical properties.

Glass-Ceramic Materials with Luminescent Properties in the System ZnO-B2O3-Nb2O5-Eu2O3

In this paper, the crystallization behavior of 50ZnO:47B2O3:3Nb2O3:0.5Eu2O3 (G-0 h) glass has been investigated in detail by DSC, XRD and TEM analysis. The luminescent properties of the resulting glass-ceramics were also investigated. By XRD and TEM analysis, crystallization of several crystalline phases has been proved (α-Zn3B2O6, β-Zn3B2O6 and ZnNb2O6). By calculating crystal parameters, it was found that europium ions are successfully incorporated in the β-Zn3B2O6. Photo-luminescent spectra showed increased emission in the resulting glass-ceramic samples compared to the parent glass sample due to higher asymmetry of Eu3+ ions in the obtained crystalline phases. It was established that the optimum emission intensity is registered for glass-ceramic samples obtained after 25 h heat treatment of the parent glass.

Prolonging a discrete time crystal by quantum-classical feedback

Nonequilibrium phases of quantum matter featuring time crystalline eigenstate order have been realized recently on noisy intermediate-scale quantum (NISQ) devices. While ideal quantum time crystals exhibit collective subharmonic oscillations and spatiotemporal long-range order persisting for infinite times, the decoherence time of current NISQ devices sets a natural limit to the survival of these phases, restricting their observation to a shallow quantum circuit. Here we propose a time-periodic scheme that leverages quantum-classical feedback protocols in subregions of the system to enhance a time crystal signal significantly exceeding the decoherence time of the device. As a case of study, we demonstrate the survival of the many-body localized discrete time crystal phase in the one-dimensional periodically kicked Ising model, accounting for decoherence of the system with an environment. Based on classical simulation of quantum circuit realizations we find that this approach is suitable for implementation on existing quantum hardware and presents a prospective path to simulate complex quantum many-body dynamics that transcend the low depth limit of current digital quantum computers. Published by the American Physical Society 2024