| 1. |
- Alnoor, Hatim, et al.
(författare)
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Exploring MXenes and their MAX phase precursors by electron microscopy
- 2021
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Ingår i: Materials Today Advances. - : Elsevier. - 2590-0498. ; 9
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Tidskriftsartikel (refereegranskat)abstract
- This review celebrates the width and depth of electron microscopy methods and how these have enabled massive research efforts on MXenes. MXenes constitute a powerful recent addition to 2-dimensional materials, derived from their parent family of nanolaminated materials known as MAX phases. Owing to their rich chemistry, MXenes exhibit properties that have revolutionized ranges of applications, including energy storage, electromagnetic interference shielding, water filtering, sensors, and catalysis. Few other methods have been more essential in MXene research and development of corresponding applications, compared with electron microscopy, which enables structural and chemical identification at the atomic scale. In the following, the electron microscopy methods that have been applied to MXene and MAX phase precursor research are presented together with research examples and are discussed with respect to advantages and challenges.
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| 2. |
- Bairagi, Samiran, et al.
(författare)
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Formation of quaternary Zn(AlxGa1−x)2O4 epilayers driven by thermally induced interdiffusion between spinel ZnGa2O4 epilayer and Al2O3 substrate
- 2023
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Ingår i: Materials Today Advances. - : Elsevier. - 2590-0498. ; 20
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Tidskriftsartikel (refereegranskat)abstract
- Zinc aluminogallate, Zn(AlxGa1−x)2O4 (ZAGO), a single-phase spinel structure, offers considerable potential for high-performance electronic devices due to its expansive compositional miscibility range between aluminum (Al) and gallium (Ga). Direct growth of high-quality ZAGO epilayers however remains problematic due to the high volatility of zinc (Zn). This work highlights a novel synthesis process for high-quality epitaxial quaternary ZAGO thin films on sapphire substrates, achieved through thermal annealing of a ZnGa2O4 (ZGO) epilayer on sapphire in an ambient air setting. In-situ annealing x-ray diffraction measurements show that the incorporation of Al in the ZGO epilayer commenced at 850 °C. The Al content (x) in ZAGO epilayer gradually increased up to around 0.45 as the annealing temperature was raised to 1100 °C, which was confirmed by transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy. X-ray rocking curve measurement revealed a small full width at half maximum value of 0.72 °, indicating the crystal quality preservation of the ZAGO epilayer with a high Al content. However, an epitaxial intermediate �–(AlxGa1−x)2O3 layer (� - AGO) was formed between the ZAGO and sapphire substrate. This is believed to be a consequence of the interdiffusion of Al and Ga between the ZGO thin film and sapphire substrate. Using density functional theory, the substitution cost of Ga in sapphire was determined to be about 0.5 eV lower than substitution cost of Al in ZGO. Motivated by this energetically favorable substitution, a formation mechanism of the ZAGO and AGO layers was proposed. Spectroscopic ellipsometry studies revealed an increase in total thickness of the film from 105.07 nm (ZGO) to 147.97 nm (ZAGO/AGO) after annealing to 1100 °C, which were corroborated using TEM. Furthermore, an observed increase in the direct (indirect) optical bandgap from 5.06 eV (4.7 eV) to 5.72 eV (5.45 eV) with an increasing Al content in the ZAGO layer further underpins the formation of a quaternary ZAGO alloy with a tunable composition.
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| 3. |
- Chouke, Prashant B., et al.
(författare)
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Bioinspired metal/metal oxide nanoparticles: A road map to potential applications
- 2022
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Ingår i: Materials Today Advances. - : Elsevier Ltd. - 2590-0498. ; 16
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Tidskriftsartikel (refereegranskat)abstract
- Manufacturing of metal and metal oxide nanoparticles (M/MO NPs) in large quantities needed a strong reliable, sustainable, and eco-friendly protocol. Present work represents on biogenic approaches to fabricate green nanoparticles using green technology. The fabrications of M/MO NPs using natural bio-resources were engaged by means of alternative technique in place of conventional methods. These methods are naturally benign, straightforward, economical, and renewed technology; they does not content harmful chemicals, zero contaminants, and eco-friendly. The extracts from the biogenic resources are widely accepted owing to its capability to minimise and control the size and shape of metal and metal oxides NPs because of different structure directing agents, usually bioorganic phyto-chemicals. In this present review, we have summarized fabrication of different NPs like silver, gold, copper oxide, cobalt oxide, titanium oxide, cerium oxide, bismuth oxide, zinc oxide and nickel oxide nanoparticles using natural resources. The challenges, limiting factors and future directions of the bioinspired synthesis of metal/metal oxide NPs are also highlighted in this review. Moreover, biogenic materials has explored for further environmental remediation in terms of photocatalytic activity, elimination of organic waste, and antibacterial, antioxidant assay, and protein-metal complexes binding affinities by molecular docking.
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| 4. |
- Horng, Ray-Hua, et al.
(författare)
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Growth mechanism and characteristics of beta-Ga2O3 heteroepitaxailly grown on sapphire by metalorganic chemical vapor deposition
- 2022
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Ingår i: Materials Today Advances. - : ELSEVIER. - 2590-0498. ; 16
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Tidskriftsartikel (refereegranskat)abstract
- In this study, monoclinic gallium oxide (beta-Ga2O3) epilayer was successfully grown on c-plane, (0001), sapphire substrate by metalorganic chemical vapor deposition (MOCVD) with interplaying growth temperature, TEGa flow rate, and growth time. X-ray diffraction 20 scans show only three narrow diffraction peaks referred to beta-Ga2O3 ((2) over bar 01), ((4) over bar 02), and ((6) over bar 03) in all epilayers, indicating a superior crystalline quality. Current-voltage (I-V) measurement reveals that these beta-Ga2O3 films are insulating and exhibit high resistance in a range of 10(12)-10(14) Omega. The crystallization characteristics of the epilayers can be effectively improved with thickness through increasing TEGa flow rate and growth time, which was evidenced by X-ray rocking curves and I-V measurements. However, the surface roughness of beta-Ga2O3 film increases with growth time and TEGa flow rate. When the growth temperature increases above 825 degrees C, the thickness of beta-Ga2O3 film decreases clearly. Furthermore, it can be found that the growth rate decreased as the growth time increasing. The growth mechanism based on first-principles calculation was proposed as that 3D growth induced by the lattice mismatch between beta-Ga2O3 and sapphire starts at nucleation stage, and follows up a lateral growth promoting a 2D growth after the thick epilayer being grown. In addition, the complex chemical reaction between TEGa and oxygen precursors was unraveled by density function theory calculation. (c) 2022 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
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| 5. |
- Kim, Jongho, et al.
(författare)
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Remarkable conductivity enhancement in P-doped polythiophenes via rational engineering of polymer-dopant interactions
- 2023
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Ingår i: Materials Today Advances. - : Elsevier BV. - 2590-0498. ; 18
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Tidskriftsartikel (refereegranskat)abstract
- Molecular doping is an effective approach to tune the charge density and optimize electrical performance of conjugated polymers. However, the introduction of dopants, on the other hand, may disturb the polymer microstructure and disrupt the charge transport path, often leading to a decrease of charge carrier mobility and deterioration of electrical conductivity of the doped films. Here we show that dopant-induced disorder can be overcome by rational engineering of polymer-dopant interactions, resulting in remarkable enhancement of electrical conductivity. Benchmark poly(3-hexylthiophene) (P3HT) and its analogous random polymers of 3-hexylthiophene and thiophene P[(3HT)1-x-stat-(T)x] were synthesized and doped by 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ). Remarkably, random P[(3HT)1-x-stat-(T)x] was doped to a far superior electrical conductivity, that in the case of x ≥ 0.24, the conductivity of P[(3HT)1-x-stat-(T)x] is over 100 times higher than that of the doped P3HT, despite both P3HT and P[(3HT)1-x-stat-(T)x] exhibit comparable charge carrier mobility in their pristine state and in spite of their practically identical redox properties. This result can be traced back to the formation of π-stacked polymer-dopant-polymer co-crystals exhibiting extremely short packing distances of 3.13–3.15 Å. The mechanism behind these performances is based on a new role played by the dopant molecules that we name “bridging-gluing”. The results are coherently verified by the combination of optical absorption spectroscopy, X-ray diffraction, density functional theory calculations, and molecular dynamics simulations.
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| 6. |
- Naeimipour, Sajjad, et al.
(författare)
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Multimodal and dynamic cross-linking of modular thiolated alginate-based bioinks
- 2023
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Ingår i: Materials Today Advances. - : ELSEVIER. - 2590-0498. ; 19
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Tidskriftsartikel (refereegranskat)abstract
- Engineered extracellular matrix-mimicking hydrogels can facilitate 3D cell culture and fabrication of tissue-like constructs and biologically relevant disease models. Processing of cell-laden hydrogels using additive manufacturing techniques further allows for the development of tissue-mimetic structures with higher spatial complexity. Whereas a wide range of printable hydrogels is available, they tend to lack biological functionality and cell compatibility. Here we show an enzymatically mediated thiol-based cross-linking strategy for the design of modular and cytocompatible hydrogel-based bioinks for 3D bioprinting of dynamic multi-material architectures. Alginate is functionalized with cysteines modified with an enzyme-labile thiol protection group. Deprotection using penicillin G acylase (PGA) generates free thiols on-demand, enabling hydrogel cross-linking using thiol-reactive cross-linkers and intermolecular disulfides while avoiding undesired and uncontrolled thiol oxidation. Remaining free thiols can be used for post-printing hydrogel functionalization and lamination of multilayer structures. Moreover, the addition of PGA to a thermo-reversible hydrogel support bath enables the bioprinting of cell-laden 3D structures with high cell viability and excellent shape fidelity. The possibilities to enzymatically generate free thiols during bioprinting facilitate cross-linking and tuning of bioink properties using cytocompatible chemistries and allow for the printing of complex and dynamic cell-laden structures.
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| 7. |
- Sheikh, S., et al.
(författare)
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Alloying effect on the oxidation behavior of a ductile Al0.5Cr0.25Nb0.5Ta0.5Ti1.5 refractory high-entropy alloy
- 2020
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Ingår i: Materials Today Advances. - : Elsevier BV. - 2590-0498. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- Refractory high-entropy alloys (RHEAs) are widely studied because of their promising potential for ultrahigh-temperature applications. One key challenge towards the development of RHEAs as high temperature structural materials is to concurrently achieve optimum oxidation resistance and mechanical properties. Here in this work, the effect of alloying on the oxidation behavior of ductile RHEAs was studied. Specifically, a ductile RHEA, Al0.5Cr0.25Nb0.5Ta0.5Ti1.5, was alloyed with Al and Zr aiming to improve its oxidation resistance. The two modified RHEAs, Al0.75Cr0.25Nb0.5Ta0.5Ti1.5 and Al0.5Cr0.25Nb0.5Ta0.5Ti1.5Zr0.01, indeed show enhanced oxidation resistance at 800 degrees C and 1,100 degrees C, compared with Al0.5Cr0.25Nb0.5Ta0.5Ti1.5. In addition, all three RHEAs studied here show an excellent oxidation resistance at 800 degrees C compared with other RHEAs, although there is still a large space to further improve their performance at 1,100 degrees C. Internal oxidation and even nitridation are still present after oxidation exposure, indicating further efforts are required to form protective oxide scales on the surface of ductile RHEAs. Nevertheless, the work is expected to shed some light on future directions of improving the oxidation of ductile RHEAs, via the alloying route.
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| 8. |
- Singh, Deobrat, et al.
(författare)
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2D Janus and non-Janus diamanes with an in-plane negative Poisson's ratio for energy applications
- 2022
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Ingår i: Materials Today Advances. - : Elsevier. - 2590-0498. ; 14
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Tidskriftsartikel (refereegranskat)abstract
- Motivated by the successful synthesis of 2D C2F diamanes [Bakharev, P.V. et al., Nat. Nanotechnol. 15, 59-66 (2020)], we have systematically investigated the structural stability, in-plane mechanical, optoelectronic, photocatalytic, piezoelectric, and thermoelectric properties of non-Janus and Janus diamanes monolayers named as C2H, C2F, C2Cl, C4HF, C4HCl and C4FCl. The structural stability is confirmed by cohesive energy, phonon dispersion spectra, and mechanical properties. The electronic properties has been calculated by HSE06 functional and the band gap are found to be 3.85, 5.64, 2.32, 4.16, 0.73 and 1.91 eV for C-2H, C2F, C2Cl, C4HF, C4HCl and C4FCl, respectively. The hydrogen-containing non-Janus and Janus diamanes monolayers have a higher negative Poisson's ratio (NPR) and therefore are good auxetic materials. From the Poisson's ratio and Young's modulus of each configuration of non-Janus and Janus diamanes monolayer, anisotropic behavior was displayed. From the optical properties calculations, the refractive index values are around 1.5, which means that it will be a transparent monolayered materials. Also, C2Cl, C4HCl and C4FCl monolayers displayed high absorption spectra with an order of 105 cm(-1) in the visible region, which shows great applications in optoelectronic devices. Additionally, the valence and conduction band-edge positions of 2D Janus and non-Janus diamanes of C2H, C2F, and C2Cl and C4HF monolayers have to straddle the redox potentials of water. It means that the photogenerated electrons and holes are sufficient to drive the overall water splitting. Whereas non-Janus diamanes C4HCl, and C4FCl monolayers displayed only water oxidation. The investigated in-plane piezoelectric coefficient has larger in non-Janus diamanes C4HF, C4HCl, and C4FCl monolayers. Therefore, it is very useful in the field of piezoelectric applications. From the thermoelectric properties, the non-Janus and Janus diamanes monolayers have great thermoelectric efficiency and were found to be 10.52 and 10.63% for C2H and C2F, respectively. Our results demonstrate the new class of 2D carbon-based monolayers has good auxetic materials as well as a wide range of applications in optoelectronics, piezoelectric, and thermoelectric fields. (C)& nbsp;2022 The Authors. Published by Elsevier Ltd.& nbsp;
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| 9. |
- Xu, Chao, et al.
(författare)
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Microporous organic polymers as CO2 adsorbents : advances and challenges
- 2020
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Ingår i: Materials Today Advances. - : Elsevier BV. - 2590-0498. ; 6
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Forskningsöversikt (refereegranskat)abstract
- Microporous organic polymers (MOPs) with internal pores less than 2 nm have potential use in gas separation, sensing, and storage, in the form of membranes, monoliths, fibers, or adsorbent granules. These covalently bonded polymers are being formed by reacting with rigid organic monomers, and MOPs have lately been studied for capturing CO2 from gas mixtures in the form of membranes and adsorbents. Especially, the potential of MOPs in the processes of carbon capture and storage has been in the focus and small pore MOPs are preferred for regular separation processes but larger pores could be suitable if cryogenic processes would be used. Recent studies (2014 – mid 2019) on the potential use of MOPs as CO2 adsorbents and, to some degree, CO2-selective membranes are reviewed.
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