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Journal articles on the topic 'Mesostructured'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 March 2023

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1

Hollergschwandtner, Elena, Thomas Schwaha, Josef Neumüller, Ulrich Kaindl, Daniela Gruber, Margret Eckhard, Michael Stöger-Pollach, and Siegfried Reipert. "Novel mesostructured inclusions in the epidermal lining of Artemia franciscana ovisacs show optical activity." PeerJ 5 (October 27, 2017): e3923. http://dx.doi.org/10.7717/peerj.3923.

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Background Biomineralization, e.g., in sea urchins or mollusks, includes the assembly of mesoscopic superstructures from inorganic crystalline components and biopolymers. The resulting mesocrystals inspire biophysicists and material scientists alike, because of their extraordinary physical properties. Current efforts to replicate mesocrystal synthesis in vitro require understanding the principles of their self-assembly in vivo. One question, not addressed so far, is whether intracellular crystals of proteins can assemble with biopolymers into functional mesocrystal-like structures. During our electron microscopy studies into Artemia franciscana (Crustacea: Branchiopoda), we found initial evidence of such proteinaceous mesostructures. Results EM preparations with high-pressure freezing and accelerated freeze substitution revealed an extraordinary intracellular source of mesostructured inclusions in both the cyto-and nucleoplasm of the epidermal lining of ovisacs of A. franciscana. Confocal reflection microscopy not only confirmed our finding; it also revealed reflective, light dispersing activity of these flake-like structures, their positioning and orientation with respect to the ovisac inside. Both the striation of alternating electron dense and electron-lucent components and the sharp edges of the flakes indicate self-assembly of material of yet unknown origin under supposed participation of crystallization. However, selected area electron diffraction could not verify the status of crystallization. Energy dispersive X-ray analysis measured a marked increase in nitrogen within the flake-like inclusion, and the almost complete absence of elements that are typically involved in inorganic crystallization. This rise in nitrogen could possibility be related to higher package density of proteins, achieved by mesostructure assembly. Conclusions The ovisac lining of A. franciscana is endowed with numerous mesostructured inclusions that have not been previously reported. We hypothesize that their self-assembly was from proteinaceous polycrystalline units and carbohydrates. These mesostructured flakes displayed active optical properties, as an umbrella-like, reflective cover of the ovisac, which suggests a functional role in the reproduction of A. franciscana. In turn, studies into ovisac mesostructured inclusions could help to optimizing rearing Artemia as feed for fish farming. We propose Artemia ovisacs as an in vivo model system for studying mesostructure formation.

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2

Wakabayashi, Ryutaro, and Tatsuo Kimura. "Surfactant-Assisted Mesostructural Variation by the Molecular Structure of Frameworks." Journal of Nanoscience and Nanotechnology 20, no. 5 (May 1, 2020): 3078–83. http://dx.doi.org/10.1166/jnn.2020.17478.

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Typical syntheses for the mesostructural design were performed with strategic deviations, being substantially powerful for changing the molecular structure of frameworks, from the synthetic conditions optimized for the preparation of lamellar and 2-d hexagonal mesostructured materials where the frameworks were constructed by aluminophosphate (AlPO) like units with and without organic groups in the molecular scale. A series of the materials such as mesostructured aluminum organophosphonate (AOP) and AlPO type ones were investigated according to the molecular structure and crystallinity of inorganic–organic hybrid and non-hybrid inorganic frameworks. Considering a uniqueness of AlPO based frameworks, a rational insight on strength of interactions between crystalline/amorphous AlPO based units and cationic surfactant molecules was surveyed as one of the most significant factors for understanding the mesostructural variation.

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3

Lai, Hongwei, Qiang Wu, Jin Zhao, Longmei Shang, He Li, Renchao Che, Zhiyang Lyu, et al. "Mesostructured NiO/Ni composites for high-performance electrochemical energy storage." Energy & Environmental Science 9, no. 6 (2016): 2053–60. http://dx.doi.org/10.1039/c6ee00603e.

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The mesostructured NiO/Ni composites boost the electrochemical energy storage performance of NiO to its theoretical limit, which results from the synergism of high accessibility to electrolyte, short solid-state ion diffusion length and high conductivity owing to the unique mesostructure.

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4

Pan, Jia Hong, Seung Yong Chai, and Wan In Lee. "Photocatalytic Properties of Mesoporous TiO₂ Films Derived from Evaporation-Induced Self-Assembly Method." Materials Science Forum 510-511 (March 2006): 58–61. http://dx.doi.org/10.4028/www.scientific.net/msf.510-511.58.

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Hexagonal and cubic mesoporous TiO2 films were prepared by using triblock copolymer-templated sol-gel method via evaporation-induced self-assembly (EISA) process. The mesophase of TiO2 film was controlled by spin-speed during the spin-coating process. The hexagonal mesoporous structure was formed at a high spin-speed around 2000 rpm, whereas the cubic mesostructure was formed at a low spin-speed around 600 rpm. XRD and TEM results indicate that those mesostructures are highly organized with a pore diameter of 7 nm. The prepared cubic and hexagonal mesoporous films were tested as photocatalysts for the decomposition of 2-propanol in gas phase. Both films presented considerably higher photocatalytic activity than a nonporous TiO2 films prepared by a typical sol-gel process without addition of triblock copolymer. Notably, we found that the cubic mesoporous films showed a relatively higher photocatalytic activity than the hexagonal mesostructured film. We believe this is due to the orientation of pore channels open on the surface of mesoporous films.

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5

Ning, Hailong, James H. Pikul, Runyu Zhang, Xuejiao Li, Sheng Xu, Junjie Wang, John A. Rogers, William P. King, and Paul V. Braun. "Holographic patterning of high-performance on-chip 3D lithium-ion microbatteries." Proceedings of the National Academy of Sciences 112, no. 21 (May 11, 2015): 6573–78. http://dx.doi.org/10.1073/pnas.1423889112.

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As sensors, wireless communication devices, personal health monitoring systems, and autonomous microelectromechanical systems (MEMS) become distributed and smaller, there is an increasing demand for miniaturized integrated power sources. Although thin-film batteries are well-suited for on-chip integration, their energy and power per unit area are limited. Three-dimensional electrode designs have potential to offer much greater power and energy per unit area; however, efforts to date to realize 3D microbatteries have led to prototypes with solid electrodes (and therefore low power) or mesostructured electrodes not compatible with manufacturing or on-chip integration. Here, we demonstrate an on-chip compatible method to fabricate high energy density (6.5 μWh cm−2⋅μm−1) 3D mesostructured Li-ion microbatteries based on LiMnO2 cathodes, and NiSn anodes that possess supercapacitor-like power (3,600 μW cm−2⋅μm−1 peak). The mesostructured electrodes are fabricated by combining 3D holographic lithography with conventional photolithography, enabling deterministic control of both the internal electrode mesostructure and the spatial distribution of the electrodes on the substrate. The resultant full cells exhibit impressive performances, for example a conventional light-emitting diode (LED) is driven with a 500-μA peak current (600-C discharge) from a 10-μm-thick microbattery with an area of 4 mm2 for 200 cycles with only 12% capacity fade. A combined experimental and modeling study where the structural parameters of the battery are modulated illustrates the unique design flexibility enabled by 3D holographic lithography and provides guidance for optimization for a given application.

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6

Li, Jianquan, and Linda F. Nazar. "Mesostructured iron sulfides." Chemical Communications, no. 18 (2000): 1749–50. http://dx.doi.org/10.1039/b005574n.

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7

Malfatti, Luca, Tongjit Kidchob, Stefano Costacurta, Paolo Falcaro, Piero Schiavuta, Heinz Amenitsch, and Plinio Innocenzi. "Highly Ordered Self-Assembled Mesostructured Hafnia Thin Films: An Example of Rewritable Mesostructure." Chemistry of Materials 18, no. 19 (September 2006): 4553–60. http://dx.doi.org/10.1021/cm060236n.

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8

MacLachlan, Mark J., Neil Coombs, Robert L. Bedard, Steve White, Laurence K. Thompson, and Geoffrey A. Ozin. "Mesostructured Metal Germanium Sulfides." Journal of the American Chemical Society 121, no. 51 (December 1999): 12005–17. http://dx.doi.org/10.1021/ja992663q.

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9

Kim, S. S. "Ultrastable Mesostructured Silica Vesicles." Science 282, no. 5392 (November 13, 1998): 1302–5. http://dx.doi.org/10.1126/science.282.5392.1302.

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10

Tian, Bozhi, Sahadev A. Shankarappa, Homer H. Chang, Rong Tong, and Daniel S. Kohane. "Biodegradable Mesostructured Polymer Membranes." Nano Letters 13, no. 9 (August 21, 2013): 4410–15. http://dx.doi.org/10.1021/nl402251x.

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11

Egger, Sam M., Katie R. Hurley, Ashish Datt, Garrett Swindlehurst, and Christy L. Haynes. "Ultraporous Mesostructured Silica Nanoparticles." Chemistry of Materials 27, no. 9 (April 21, 2015): 3193–96. http://dx.doi.org/10.1021/cm504448u.

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12

Ayyappan, S., N. Ulagappan, and C. N. R. Rao. "Mesostructured lamellar chromium oxide." Journal of Materials Chemistry 6, no. 10 (1996): 1737. http://dx.doi.org/10.1039/jm9960601737.

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13

Roy, Xavier, Laurence K Thompson, Neil Coombs, and Mark J MacLachlan. "Mesostructured Prussian Blue Analogues." Angewandte Chemie 120, no. 3 (January 4, 2008): 521–24. http://dx.doi.org/10.1002/ange.200703627.

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14

Roy, Xavier, Laurence K Thompson, Neil Coombs, and Mark J MacLachlan. "Mesostructured Prussian Blue Analogues." Angewandte Chemie International Edition 47, no. 3 (January 4, 2008): 511–14. http://dx.doi.org/10.1002/anie.200703627.

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15

Zhang, Jun, Meihua Yu, Pei Yuan, Hongning Wang, Kun Qian, Lei Tan, Yunhua Wang, and Chengzhong Yu. "Tuning cooperative vesicle templating and liquid crystal templating simply by varying silica source." Journal of Materials Research 25, no. 4 (April 2010): 648–57. http://dx.doi.org/10.1557/jmr.2010.0085.

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The cooperative self-assembly of organic–inorganic siliceous composite structures has been studied from the aspect of inorganic precursors. We reveal that the vesicular or mesostructured materials can be obtained selectively by just changing the silica sources in one templating system. For poly(ethylene oxide)-type block copolymers with either poly(propylene oxide) or poly(butylene oxide) as the hydrophobic moieties, when the other synthesis parameters are exactly the same, the use of tetramethyl orthosilicate (TMOS) as a silica source gives rise to highly ordered mesostructures, while the use of tetraethyl orthosilicate (TEOS) leads to vesicles or foams. The attenuated total reflection Fourier transform infrared (ATR-FTIR) technique is used to monitor the silicate species derived from the hydrolysis and condensation of TMOS and TEOS as a function of the reaction time. On the basis of the ATR-FTIR results, we propose a “differentiating effect” at relatively high pH (4.7) to interpret the influence of different silica sources on the self-organized composite structures. For comparison, a “leveling effect” at relatively low pH (strong acidic conditions) is revealed to explain that both TMOS and TEOS lead to the same mesostructures. Our contribution provides a feasible and designable method to synthesize from conventional ordered mesostructures to novel vesicular structures, which are significant for their future practical applications.

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16

Secci, Fausto, Marco Sanna Angotzi, Valentina Mameli, Sarah Lai, Patrícia A. Russo, Nicola Pinna, Mauro Mureddu, Elisabetta Rombi, and Carla Cannas. "Mesostructured γ-Al2O3-Based Bifunctional Catalysts for Direct Synthesis of Dimethyl Ether from CO2." Catalysts 13, no. 3 (February 28, 2023): 505. http://dx.doi.org/10.3390/catal13030505.

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In this work, we propose two bifunctional nanocomposite catalysts based on acidic mesostructured γ-Al2O3 and a Cu/ZnO/ZrO2 redox phase. γ-Al2O3 was synthesized by an Evaporation-Induced Self-Assembly (EISA) method using two different templating agents (block copolymers Pluronic P123 and F127) and subsequently functionalized with the redox phase using an impregnation method modified with a self-combustion reaction. These nanocomposite catalysts and their corresponding mesostructured supports were characterized in terms of structural, textural, and morphological features as well as their acidic properties. The bifunctional catalysts were tested for the CO2-to-DME process, and their performances were compared with a physical mixture consisting of the most promising support as a dehydration catalyst together with the most common Cu-based commercial redox catalyst (CZA). The results highlight that the most appropriate Pluronic for the synthesis of γ-Al2O3 is P123; the use of this templating agent allows us to obtain a mesostructure with a smaller pore size and a higher number of acid sites. Furthermore, the corresponding composite catalyst shows a better dispersion of the redox phase and, consequently, a higher CO2 conversion. However, the incorporation of the redox phase into the porous structure of the acidic support (chemical mixing), favoring an intimate contact between the two phases, has detrimental effects on the dehydration performances due to the coverage of the acid sites with the redox nanophase. On the other hand, the strategy involving the physical mixing of the two phases, distinctly preserving the two catalytic functions, assures better performances.

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17

Yada, Mitsunori, Hiroki Tanaka, Masato Akiyama, Takeru Kitajima, Yuko Inoue, and Takanori Watari. "Enhancing Heat Resistance of Red Color by Coating Fe₂O₃ Nanoparticles with Mesostructured Silica." Key Engineering Materials 878 (March 2021): 49–55. http://dx.doi.org/10.4028/www.scientific.net/kem.878.49.

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The surface of α-Fe2O3 nanoparticles was successfully coated with mesostructured silica templated by surfactant assemblies using cetyltrimethylammonium ions. By repeating the coating operation, it was possible to control the thickness of the mesostructured silica phase. In the sample obtained with ten coatings, in particular, the aggregation and sintering of the α-Fe2O3 nanoparticles was suppressed, and the bright red before the heat treatment was maintained even after a heat treatment at 1300 °C.

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18

Beekman, Matt, Susan Kauzlarich, Luke Doherty, and George Nolas. "Zintl Phases as Reactive Precursors for Synthesis of Novel Silicon and Germanium-Based Materials." Materials 12, no. 7 (April 8, 2019): 1139. http://dx.doi.org/10.3390/ma12071139.

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Recent experimental and theoretical work has demonstrated significant potential to tune the properties of silicon and germanium by adjusting the mesostructure, nanostructure, and/or crystalline structure of these group 14 elements. Despite the promise to achieve enhanced functionality with these already technologically important elements, a significant challenge lies in the identification of effective synthetic approaches that can access metastable silicon and germanium-based extended solids with a particular crystal structure or specific nano/meso-structured features. In this context, the class of intermetallic compounds known as Zintl phases has provided a platform for discovery of novel silicon and germanium-based materials. This review highlights some of the ways in which silicon and germanium-based Zintl phases have been utilized as precursors in innovative approaches to synthesize new crystalline modifications, nanoparticles, nanosheets, and mesostructured and nanoporous extended solids with properties that can be very different from the ground states of the elements.

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19

Gao, Qian, Wei-Tao Zheng, Cun-Di Wei, and Hui-Ming Lin. "Methanol-Sensing Property Improvement of Mesostructured Zinc Oxide Prepared by the Nanocasting Strategy." Journal of Nanomaterials 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/263852.

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The specific structure and morphology often play a critical role in governing the excellent intrinsic properties of the compound semiconductor. Herein, mesostructured ZnO with excellent methanol-sensing properties was prepared by a structure replication procedure through the incipient wetness technique. The investigation on the crystal structure and morphology of the resultant material shows that the product consists of hexagonally arranged mesopores and crystalline walls, and its structure is an ideal replication of CMK-3 template. Consequently, mesostructured ZnO was fabricated as a gas sensor for methanol. The excellent methanol-sensing performance was achieved at a relatively low operating temperature of 120°C. In comparison with the nonporous ZnO prepared through conventional coprecipitation approach, mesostructured ZnO material shows the higher sensitivity and stability. Furthermore, it shows the discrimination between methanol and ethanol sensitivity, which makes it a good candidate in fabricating selective methanol sensor in practice.

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20

Yu, K., X. Wu, C. J. Brinker, and J. Ripmeester. "Mesostructured MTES-Derived Silica Thin Film with Spherical Voids Investigated by TEM: 1. Mesostructure Determination." Langmuir 19, no. 18 (September 2003): 7282–88. http://dx.doi.org/10.1021/la034310h.

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21

Mizoshita, Norihiro, Masamichi Ikai, Takao Tani, and Shinji Inagaki. "Hole-Transporting Periodic Mesostructured Organosilica." Journal of the American Chemical Society 131, no. 40 (October 14, 2009): 14225–27. http://dx.doi.org/10.1021/ja9050263.

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22

Bryjak, Jolanta, Katarzyna Szymańska, and Andrzej B. Jarzębski. "Laccase Immobilisation on Mesostructured Silicas." Chemical and Process Engineering 33, no. 4 (December 1, 2012): 611–20. http://dx.doi.org/10.2478/v10176-012-0051-9.

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Extracellular laccase produced by the wood-rotting fungus Cerrena unicolor was immobilised covalently on the mesostructured siliceous foam (MCF) and three hexagonally ordered mesoporous silicas (SBA-15) with different pore sizes. The enzyme was attached covalently via glutaraldehyde (GLA) or by simple adsorption and additionally crosslinked with GLA. The experiments indicated that laccase bound by covalent attachment remains very active and stable. The best biocatalysts were MCF and SBA-15 with Si-F moieties on their surface. Thermal inactivation of immobilised and native laccase at 80°C showed a biphasic-type activity decay, that could be modelled with 3- parameter isoenzyme model. It appeared that immobilisation did not significantly change the mechanism of activity loss but stabilised a fraction of a stable isoform. Examination of time needed for 90% initial activity loss revealed that immobilisation prolonged that time from 8 min (native enzyme) up to 155 min (SBA-15SF).

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23

Schulz, M., M. Tiemann, M. Fröba, and C. Jäger. "NMR Characterization of Mesostructured Aluminophosphates." Journal of Physical Chemistry B 104, no. 45 (November 2000): 10473–81. http://dx.doi.org/10.1021/jp000337n.

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24

Shi, Li Ying, Jian Qiang Wang, Ling Gao, Li Huang, Jianhua Zhu, Ying Wang, Xiaoxing Fan, et al. "Preparation of Mesostructured Lamellar Zirconia." Materials and Manufacturing Processes 22, no. 6 (June 29, 2007): 705–9. http://dx.doi.org/10.1080/10426910701385010.

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25

Carreon, Moises A., and Vadim V. Guliants. "Mesostructured vanadium-phosphorus-oxide phases." Microporous and Mesoporous Materials 55, no. 3 (September 2002): 297–304. http://dx.doi.org/10.1016/s1387-1811(02)00432-8.

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26

Liu, Ping, Igor L. Moudrakovski, Jun Liu, and Abdelhamid Sayari. "Mesostructured Vanadium Oxide Containing Dodecylamine⊥." Chemistry of Materials 9, no. 11 (November 1997): 2513–20. http://dx.doi.org/10.1021/cm970067u.

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27

Petkov, N., S. Mintova, B. Jean, T. Metzger, and T. Bein. "Functionalized cubic mesostructured silica films." Materials Science and Engineering: C 23, no. 6-8 (December 2003): 827–31. http://dx.doi.org/10.1016/j.msec.2003.09.134.

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28

Malik, Abds-Sami, Morven J. Duncan, and Peter G. Bruce. "Mesostructured iron and manganese oxides." Journal of Materials Chemistry 13, no. 9 (2003): 2123. http://dx.doi.org/10.1039/b303551d.

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29

Sayari, Abdelhamid, Vanaja R. Karra, J. Sudhakar Reddy, and Igor L. Moudrakovski. "Synthesis of mesostructured lamellar aluminophosphates." Chemical Communications, no. 3 (1996): 411. http://dx.doi.org/10.1039/cc9960000411.

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30

Innocenzi, Plinio, Tongjit Kidchob, Paolo Falcaro, and Masahide Takahashi. "Patterning Techniques for Mesostructured Films†." Chemistry of Materials 20, no. 3 (February 2008): 607–14. http://dx.doi.org/10.1021/cm071784j.

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31

Shah, Jainisha, and Thomas J. Pinnavaia. "Thiol-functionalized mesostructured silica vesicles." Chemical Communications, no. 12 (2005): 1598. http://dx.doi.org/10.1039/b413265c.

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32

Khimyak, Yaroslav Z., and Jacek Klinowski. "Synthesis of new mesostructured aluminophosphates." Journal of the Chemical Society, Faraday Transactions 94, no. 15 (1998): 2241–47. http://dx.doi.org/10.1039/a802221f.

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33

Huang, Yinyan, and Wolfgang M. H. Sachtler. "Preparation of mesostructured lamellar zirconia." Chemical Communications, no. 13 (1997): 1181–82. http://dx.doi.org/10.1039/a700974g.

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34

Fröba, Michael, and Nadine Oberender. "First synthesis of mesostructured thiogermanates." Chemical Communications, no. 18 (1997): 1729–30. http://dx.doi.org/10.1039/a703634e.

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35

Zhang, Zhaorong, Randall W. Hicks, Thomas R. Pauly, and Thomas J. Pinnavaia. "Mesostructured Forms of γ-Al2O3." Journal of the American Chemical Society 124, no. 8 (February 2002): 1592–93. http://dx.doi.org/10.1021/ja016974o.

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36

Johansson, Erik, Eunshil Choi, Sarah Angelos, Monty Liong, and Jeffrey I. Zink. "Light-activated functional mesostructured silica." Journal of Sol-Gel Science and Technology 46, no. 3 (December 19, 2007): 313–22. http://dx.doi.org/10.1007/s10971-007-1661-4.

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37

Kim, C. H., S. S. Kim, F. Guo, T. P. Hogan, and T. J. Pinnavaia. "Polymer Intercalation in Mesostructured Carbon." Advanced Materials 16, no. 8 (April 19, 2004): 736–39. http://dx.doi.org/10.1002/adma.200305692.

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38

Kanatzidis, M. G. "Beyond Silica: Nonoxidic Mesostructured Materials." Advanced Materials 19, no. 9 (May 7, 2007): 1165–81. http://dx.doi.org/10.1002/adma.200601763.

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39

Fowler, C. E., D. Khushalani, B. Lebeau, and S. Mann. "Nanoscale Materials with Mesostructured Interiors." Advanced Materials 13, no. 9 (May 2001): 649–52. http://dx.doi.org/10.1002/1521-4095(200105)13:9<649::aid-adma649>3.0.co;2-g.

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40

Junggeburth, Sebastian C., Katharina Schwinghammer, Kulpreet S. Virdi, Christina Scheu, and Bettina V. Lotsch. "Towards Mesostructured Zinc Imidazolate Frameworks." Chemistry - A European Journal 18, no. 7 (January 9, 2012): 2143–52. http://dx.doi.org/10.1002/chem.201101530.

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Zhang, Hong Liang, Chang Jin Tang, Fei Gao, and Lin Dong. "Synthesis and Catalytic Activity of Fe-MCM-41 Nanoparticles." Advanced Materials Research 933 (May 2014): 17–22. http://dx.doi.org/10.4028/www.scientific.net/amr.933.17.

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Mesostructured Fe-MCM-41 nanoparticles have been hydrothermally prepared for the first time with assistance of binary surfactants (CTAB and F127). The formation of nanoparticles consists of two steps, that is, the hydrolysis of silica precursor via catalysis by an acidic ferric salt, followed by facile assembly into mesostructured nanocomposites with cationic micelles by addition of condensation catalyst. In the hydroxylation of phenol with aqueous H2O2, Fe-MCM-41-NP displayed higher activity than a Fe-MCM-41 sample with normal particle size (Fe-MCM-41-LP).

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42

Roiati, V., S. Colella, G. Lerario, L. De Marco, A. Rizzo, A. Listorti, and G. Gigli. "Investigating charge dynamics in halide perovskite-sensitized mesostructured solar cells." Energy Environ. Sci. 7, no. 6 (2014): 1889–94. http://dx.doi.org/10.1039/c3ee43991g.

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43

Naik, Parimal V., Pieter L. H. Verlooy, Sam Smet, Johan A. Martens, and Ivo F. J. Vankelecom. "PDMS mixed matrix membranes filled with novel PSS-2 nanoparticles for ethanol/water separation by pervaporation." RSC Advances 6, no. 82 (2016): 78648–51. http://dx.doi.org/10.1039/c6ra15231g.

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Naik, Parimal V., Lik H. Wee, Maria Meledina, Stuart Turner, Yanbo Li, Gustaaf Van Tendeloo, Johan A. Martens, and Ivo F. J. Vankelecom. "PDMS membranes containing ZIF-coated mesoporous silica spheres for efficient ethanol recovery via pervaporation." Journal of Materials Chemistry A 4, no. 33 (2016): 12790–98. http://dx.doi.org/10.1039/c6ta04700a.

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45

Voss, Georg J. B., Elvia A. Chavez Panduro, Anette Midttveit, Jostein B. Fløystad, Kristin Høydalsvik, Alain Gibaud, Dag W. Breiby, and Magnus Rønning. "Mesostructured alumina as powders and thin films." J. Mater. Chem. A 2, no. 25 (2014): 9727–35. http://dx.doi.org/10.1039/c4ta00604f.

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46

Malik, Ritu, Vijay K. Tomer, Vandna Chaudhary, Manjeet S. Dahiya, Anshu Sharma, S. P. Nehra, Surender Duhan, and Kamalakannan Kailasam. "An excellent humidity sensor based on In–SnO2 loaded mesoporous graphitic carbon nitride." Journal of Materials Chemistry A 5, no. 27 (2017): 14134–43. http://dx.doi.org/10.1039/c7ta02860a.

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Rather, Ryhan Abdullah, Mohd Umar Khan, and Zeba N. Siddiqui. "Sulphated alumina tungstic acid (SATA): a highly efficient and novel heterogeneous mesostructured catalyst for the synthesis of pyrazole carbonitrile derivatives and evaluation of green metrics." RSC Advances 10, no. 2 (2020): 818–27. http://dx.doi.org/10.1039/c9ra09013d.

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Yamauchi, Yusuke, Masaki Komatsu, Minekazu Fuziwara, Yoshihiro Nemoto, Keisuke Sato, Tokihiko Yokoshima, Hiroaki Sukegawa, Kouichiro Inomata, and Kazuyuki Kuroda. "Ferromagnetic Mesostructured Alloys: Design of Ordered Mesostructured Alloys with Multicomponent Metals from Lyotropic Liquid Crystals." Angewandte Chemie International Edition 48, no. 42 (October 5, 2009): 7792–97. http://dx.doi.org/10.1002/anie.200902934.

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Yamauchi, Yusuke, Masaki Komatsu, Minekazu Fuziwara, Yoshihiro Nemoto, Keisuke Sato, Tokihiko Yokoshima, Hiroaki Sukegawa, Kouichiro Inomata, and Kazuyuki Kuroda. "Ferromagnetic Mesostructured Alloys: Design of Ordered Mesostructured Alloys with Multicomponent Metals from Lyotropic Liquid Crystals." Angewandte Chemie 121, no. 42 (October 5, 2009): 7932–37. http://dx.doi.org/10.1002/ange.200902934.

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Li, Lin, Zexi Liu, Lu Han, Shunai Che, and Yingying Duan. "Chiral mesostructured hydroxide zinc carbonate for enantioseparation in high performance liquid chromatography." Chemical Communications 58, no. 25 (2022): 4040–43. http://dx.doi.org/10.1039/d1cc06813j.

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