Academic literature on the topic 'Growth and self assembly'
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Journal articles on the topic "Growth and self assembly"
Ostrikov, Kostya (Ken), Igor Levchenko, and Shuyan Xu. "Self-organized nanoarrays: Plasma-related controls." Pure and Applied Chemistry 80, no. 9 (January 1, 2008): 1909–18. http://dx.doi.org/10.1351/pac200880091909.
Full textRode, Sebastian, Jens Elgeti, and Gerhard Gompper. "Chiral-filament self-assembly on curved manifolds." Soft Matter 16, no. 46 (2020): 10548–57. http://dx.doi.org/10.1039/d0sm01339k.
Full textYasmin, Rojoba, and Russell Deaton. "Logical computation with self-assembling electric circuits." PLOS ONE 17, no. 12 (December 7, 2022): e0278033. http://dx.doi.org/10.1371/journal.pone.0278033.
Full textZhang, Wan-Cheng, Meng-Dai Luoshan, Peng-Fei Wang, Chu-Yun Huang, Qu-Quan Wang, Si-Jing Ding, and Li Zhou. "Growth of Porous Ag@AuCu Trimetal Nanoplates Assisted by Self-Assembly." Nanomaterials 10, no. 11 (November 5, 2020): 2207. http://dx.doi.org/10.3390/nano10112207.
Full textLópez-López, Máximo, Esteban Cruz-Hernández, Isaac Martínez-Velis, Juan Salvador Rojas-Ramírez, Manolo Ramirez-Lopez, and Álvaro Orlando Pulzara-Mora. "Self Assembly of semiconductor nanostructures." Respuestas 12, no. 2 (May 16, 2016): 47–51. http://dx.doi.org/10.22463/0122820x.570.
Full textRaghuwanshi, Vikram Singh, Miguel Ochmann, Frank Polzer, Armin Hoell, and Klaus Rademann. "Growth mechanisms of self-assembled gold nanoparticles in Deep Eutectic Solvent." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C891. http://dx.doi.org/10.1107/s2053273314091086.
Full textChang, Wen Ku, Yu Shiang Wu, and Zhong Han Shen. "Self-Assembly of Cuprous Oxide Micro/Nanostructures by Photo-Reduction Method." Advanced Materials Research 97-101 (March 2010): 2180–83. http://dx.doi.org/10.4028/www.scientific.net/amr.97-101.2180.
Full textWilts, Bodo D., Peta L. Clode, Nipam H. Patel, and Gerd E. Schröder-Turk. "Nature’s functional nanomaterials: Growth or self-assembly?" MRS Bulletin 44, no. 2 (February 2019): 106–12. http://dx.doi.org/10.1557/mrs.2019.21.
Full textAhn, Sungsook, Sung Yong Jung, and Sang Joon Lee. "Self-Assembly Change by Gold Nanoparticle Growth." Journal of Physical Chemistry C 115, no. 45 (October 25, 2011): 22301–8. http://dx.doi.org/10.1021/jp2085523.
Full textTanaka, Takumi, Yuki Terauchi, Akira Yoshimi, and Keietsu Abe. "Aspergillus Hydrophobins: Physicochemical Properties, Biochemical Properties, and Functions in Solid Polymer Degradation." Microorganisms 10, no. 8 (July 25, 2022): 1498. http://dx.doi.org/10.3390/microorganisms10081498.
Full textDissertations / Theses on the topic "Growth and self assembly"
Cruz, Daniel Alejandro. "Hierarchical Self-Assembly and Substitution Rules." Scholar Commons, 2019. https://scholarcommons.usf.edu/etd/7770.
Full textMolnar, G., L. Dozsa, Z. Vertesy, and Z. J. Horvath. "Thickness Dependent Growth of Epitaxial Iron Silicide Nanoobjects on Si (001)." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35180.
Full textJiang, Feng. "Ligand Controlled Growth of Aqueous II-VI Semiconductor Nanoparticles and Their Self-Assembly." Diss., The University of Arizona, 2013. http://hdl.handle.net/10150/311311.
Full textBouville, Florian. "Self-assembly of anisotropic particles driven by ice growth : Mechanisms, applications and bioinspiration." Thesis, Lyon, INSA, 2013. http://www.theses.fr/2013ISAL0155/document.
Full textSelf-assembly phenomena are of prime interest in materials science, because they fill the gap between assembly of macrostructure and processing of nanomaterials. Self-assembly is based on the spontaneous organization of individual small constituents into patterns and structures. Controlling the spatial arrangement can possibly improve materials properties by maximizing its response in a given direction. Furthermore, particular types of spatial arrangement, such as found in natural structures, can even induce new properties. During the past three years, we have used ice templating process to trigger the assembly of platelet-shaped particles to replicate the hierarchical structure of nacre. Control over this technique allowed structural customization at different length-scales: local orientation of the platelets, ice crystal long range order, and the control if the interfaces between the platelets. This hierarchical process has set the ground for the creation of a new fully mineral nacre-like alumina. The local platelet self-assembly triggered by ice growth was investigated by Discrete Element Modelling which provided new insight into the dynamic phenomenon responsible for the particles alignment. Synchrotron X-ray tomography was used to validated the model results. The different architecture observed in the final samples are not the result of a percolation threshold, as one could expect, but is instead a consequence of the delicate balance between pushing and engulfment at the solidification front. The local alignment of platelets can be beneficial for the functional and structural characteristics of composites and relevant aspects for two potential applications were investigated: the thermal properties of the hexagonal boron nitride/silicon rubber composites and the mechanical properties of macroporous alumina. Further adaptation of the process allowed for long range ordering of the ice crystals (up to the centimeter scale). Different tools have also been developed in order to characterize the response of composites as a function of the architecture at the level of the macropores and particle organisation. Once those two levels of alignment were achieved, the addition of a glassy phase and nanoparticles to the grain boundaries of the platelets introduces, just like in nacre, interfaces capable of deflect and even stopping crack propagation
Hille, Pascal [Verfasser]. "Advanced group III-nitride nanowire heterostructures - self-assembly and position-controlled growth / Pascal Hille." Gießen : Universitätsbibliothek, 2017. http://d-nb.info/1132510511/34.
Full textNardi, Elena. "Growth of organic nanostructures through on-surface reactions : from phthalocyanines self-assembly to polymeric phthalocyanines." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4351/document.
Full textSurface-assisted covalent coupling of suitably designed molecular precursors on metal surfaces has recently emerged as a new route towards the design of novel molecular architectures promising for future applications. Phthalocyanines and their derivatives have been widely studied for their chemical and optoelectronic properties. In this thesis the synthesis of phthalocyanine compounds is presented. The compounds are obtained through an on-surface reaction between tetracarbonitrile-functionalized precursors and metals. The experimental investigation is carried out by means of scanning tunnelling microscopy and X-Ray photoemission spectroscopy. Two molecular precursors, TCN-DBTTF and PPCN, are studied. TCN-DBTTF molecules are deposited with metal atoms (Mn, Fe, or Cu) on Ag(111) and Au(111). Annealing is used to activate the reaction of cyclotetramerization between precursors and metals. In the most favourable case (TCN-DBTTF with Fe on Ag(111)) the reaction can be activated at 200°C and leads to the synthesis of individual phthalocyanines. Increasing the temperature allows the synthesis of polymeric lines, at 250°C, and small 2D domains, at 275°C. Similar results are obtained for PPCN deposition with Mn or Cu on Au(111). In this latter case, the evolution of core level spectra allows a chemical proof of the on-surface reaction. The factors affecting on-surface cyclotetramerization have also been studied. This study demonstrates the versatility of the method: on-surface cyclotetramerization allows creating original 2D polymers connected by phthalocyanine macrocycles, and may work with a wide range of tetracarbonitrile-functionalized precursors and metallic atoms
Davey, Roger J. "The nucleation and growth of crystals from solution - molecular self assembly, materials science and process technology." Thesis, University of Manchester, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.525976.
Full textDahal, Yuba Raj. "Equilibrium and kinetic factors in protein crystal growth." Diss., Kansas State University, 2017. http://hdl.handle.net/2097/36220.
Full textDepartment of Physics
Jeremy D. Schmit
Diseases such as Alzheimer’s, Parkinson’s, eye lens cataracts, and Type 2 diabetes are the results of protein aggregation. Protein aggregation is also a problem in pharmaceutical industry for designing protein based drugs for long term stability. Disordered states such as precipitates and gels and ordered states such as crystals, micro tubules and capsids are both possible outcomes of protein–protein interaction. To understand the outcomes of protein–protein interaction and to find the ways to control forces, it is required to study both kinetic and equilibrium factors in protein–protein interactions. Salting in/salting out and Hofmeister effects are familiar terminologies used in protein science field from more than a century to represent the effects of salt on protein solubility, but they are yet to be understood theoretically. Here, we build a theory accounting both attractive and repulsive electrostatic interactions via the Poisson Boltzmann equation, ion–protein binding via grand cannonical partition function and implicit ion–water interaction using hydrated ion size, for describing salting in/salting out phenomena and Hofmeister and/or salt specific effect. Our model free energy includes Coulomb energy, salt entropy and ion–protein binding free energy. We find that the salting in behavior seen at low salt concentration near the isoelectric point of the protein is the output of Coulomb energy such that the addition of salt not only screens dipole attraction but also it enhances the monopole repulsion due to anion binding. The salting out behavior appearing after salting in at high salt concentration is due to a salt mediated depletion interaction. We also find that the salting out seen far from the isoelectric point of the protein is dominated by the salt entropy term. At low salt, the dominant effect comes from the entropic cost of confining ions within the aggregates and at high salt, the dominant effect comes from the entropy gain by ions in solution by enhancing the depletion attraction. The ion size has significant effects on the entropic term which leads to the salt specificity in the protein solubility. Crystal growth of anisotropic and fragile molecules such as proteins is a challenging task because kinetics search for a molecule having the correct binding state from a large ensemble of molecules. In the search process, crystal growth might suffer from a kinetic trap called self–poisoning. Here, we use Monte Carlo simulation to show why protein crystallization is vulnerable to the poisoning and how one can avoid such trap or recover crystal growth from such trap during crystallization. We show that self–poisoning requires only three minimal ingredients and these are related to the binding affinity of a protein molecule and its probability of occurrence. If a molecule attaches to the crystal in the crystallographic state then its binding energy will be high but in protein system this happens with very low probability (≈ 10−5). On the other hand, non–crystallographic binding is energetically weak, but it is highly probable to happen. If these things are realized, then it will not be surprising to encounter with self–poisoning during protein crystallization. The only way to recover or avoid poisoning is to alter the solution condition slightly such as by changing temperature or salt concentration or protein concentration etc.
Farrer, I. "Growth and applications of self-assembled quantum dots." Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.598945.
Full textYoshikawa, Taro [Verfasser], and Oliver [Akademischer Betreuer] Ambacher. "Toward ultra-thin nanocrystalline diamond film growth: electrostatic self-assembly of non-aggregated diamond nanoparticles onto substrate surfaces." Freiburg : Universität, 2017. http://d-nb.info/115294469X/34.
Full textBooks on the topic "Growth and self assembly"
A, Golovin A., Nepomni͡ashchiĭ A. A, and NATO Public Diplomacy Division, eds. Self-assembly, pattern formation and growth phenomena in nano-systems. Dordrecht: Springer, 2006.
Find full textPelesko, John A. Self Assembly. London: Taylor and Francis, 2007.
Find full textNagarajan, Ramanathan, ed. Self-Assembly. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.
Full textChen, Xi, ed. Mechanical Self-Assembly. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-4562-3.
Full textMcManus, Jennifer J., ed. Protein Self-Assembly. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9678-0.
Full textNilsson, Bradley L., and Todd M. Doran, eds. Peptide Self-Assembly. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7811-3.
Full textPreece, Jon Andrew. From self-assembly to self-organisation. Birmingham: University of Birmingham, 1994.
Find full textSelf-directed growth. Muncie, Ind: Accelerated Development, 1988.
Find full textCusack, Lucy M. Self-assembly of heterosupermolecules. Dublin: University College Dublin, 1997.
Find full textBellucci, Stefano, ed. Self-Assembly of Nanostructures. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-0742-3.
Full textBook chapters on the topic "Growth and self assembly"
Papadopoulos, Christo. "Direct-Growth and Self-assembly." In SpringerBriefs in Materials, 45–61. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31742-7_7.
Full textPersichetti, L., A. Capasso, A. Sgarlata, M. Fanfoni, N. Motta, and A. Balzarotti. "Towards a Controlled Growth of Self-assembled Nanostructures: Shaping, Ordering, and Localization in Ge/Si Heteroepitaxy." In Self-Assembly of Nanostructures, 201–63. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4614-0742-3_4.
Full textGuldin, Stefan. "Crystal Growth in Block Copolymer-Derived Mesoporous TiO $$_2$$ 2." In Inorganic Nanoarchitectures by Organic Self-Assembly, 87–100. Heidelberg: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00312-2_6.
Full textBaryshnikov, Yuliy, Ed Coffman, Nadrian Seeman, and Teddy Yimwadsana. "Self-correcting Self-assembly: Growth Models and the Hammersley Process." In DNA Computing, 1–11. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/11753681_1.
Full textHenneberger, F. "7.4.1 Self-assembled quantum dots: Introduction." In Growth and Structuring, 352–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-68357-5_64.
Full textSkjeltorp, A. T., J. Akselvoll, K. de Lange Kristiansen, G. Helgesen, R. Toussaint, E. G. Flekkøy, and J. Cernak. "Self-Assembly and Dynamics of Magnetic Holes." In Forces, Growth and Form in Soft Condensed Matter: At the Interface between Physics and Biology, 165–79. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2340-5_9.
Full textSpringholz, G., and G. Bauer. "9.6 Self-assembled Stranski-Krastanow quantum dots." In Growth and Structuring, 501–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-68357-5_93.
Full textTokar, V. I., and H. Dreyssé. "Self-Assembly of Few-Atom Clusters in a Model of a Strained Submonolayer." In Atomistic Aspects of Epitaxial Growth, 429–37. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0391-9_32.
Full textTersoff, J. "Role of Stress in the Self-Assembly of Nanostructures." In Low Dimensional Structures Prepared by Epitaxial Growth or Regrowth on Patterned Substrates, 13–17. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0341-1_2.
Full textSpringholz, G., and G. Bauer. "9.6.1 Growth of self-assembled lead-salt quantum dots." In Growth and Structuring, 503–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-68357-5_94.
Full textConference papers on the topic "Growth and self assembly"
Frechette, Stephen, Yong Bin Kim, and F. Lombardi. "Checkpointing of Rectilinear Growth in DNA Self-Assembly." In 2008 23rd IEEE International Symposium on Defect and Fault Tolerance in VLSI Systems (DFTVS). IEEE, 2008. http://dx.doi.org/10.1109/dft.2008.10.
Full textWang, Benzhong, and Soo-Jin Chua. "Self-organized growth of InP on GaAs substrate by MOCVD." In International Symposium on Microelectronics and Assembly, edited by H. Barry Harrison, Andrew T. S. Wee, and Subhash Gupta. SPIE, 2000. http://dx.doi.org/10.1117/12.405393.
Full textMasoud Hashempour, Zahra Mashreghian Arani, and Fabrizio Lombardi. "Robust self-assembly of interconnects by parallel DNA growth." In 2007 IEEE International Symposium on Nanoscale Architectures. IEEE, 2007. http://dx.doi.org/10.1109/nanoarch.2007.4400860.
Full textChandramohan, Abhishek, Nikolai Sibirev, Vladimir G. Dubrovskii, Budhika Mendis, Mike C. Petty, Andrew J. Gallant, and Dagou A. Zeze. "Self-assembly based nanometer-scale patterning for nanowire growth." In SPIE Nanoscience + Engineering, edited by Eva M. Campo, Elizabeth A. Dobisz, and Louay A. Eldada. SPIE, 2015. http://dx.doi.org/10.1117/12.2188016.
Full textKladitis, Paul E., and Victor M. Bright. "Novel Resistive Point Heater for MEMS Remote Solder Self-Assembly." In ASME 2000 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/imece2000-1087.
Full textHajilounezhad, Taher, and Matthew R. Maschmann. "Numerical Investigation of Internal Forces During Carbon Nanotube Forest Self-Assembly." In ASME 2018 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/imece2018-86567.
Full textSimmonds, Paul J. "Quantum dot growth on (111) and (110) surfaces using tensile-strained self-assembly." In Quantum Dots and Nanostructures: Growth, Characterization, and Modeling XV, edited by Diana L. Huffaker and Holger Eisele. SPIE, 2018. http://dx.doi.org/10.1117/12.2299676.
Full textWang, Yunran, Mark Hopkinson, Im Sik Han, Saraswati Behera, and Chaoyuan Jin. "Directed self-assembly of InAs quantum dots using in situ interference lithography." In Quantum Dots, Nanostructures, and Quantum Materials: Growth, Characterization, and Modeling XVII, edited by Diana L. Huffaker and Holger Eisele. SPIE, 2020. http://dx.doi.org/10.1117/12.2544875.
Full textAhn, Jaewoo, Jung Seob Shim, and Dong Hyun Lee. "Fabrication of quantum-dot light-emitting devices using template-assisted self-assembly (Conference Presentation)." In Quantum Dots and Nanostructures: Growth, Characterization, and Modeling XVI, edited by Diana L. Huffaker and Holger Eisele. SPIE, 2019. http://dx.doi.org/10.1117/12.2508452.
Full textTaylor, Curtis, Eric Stach, Gregory Salamo, and Ajay Malshe. "Nanoindentation Assisted Self-Assembly of Quantum Dots." In ASME 2006 International Manufacturing Science and Engineering Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/msec2006-21139.
Full textReports on the topic "Growth and self assembly"
Hsu, Julia W. P. Nanolithography Directed Materials Growth and Self-Assembly. Office of Scientific and Technical Information (OSTI), October 2006. http://dx.doi.org/10.2172/1137213.
Full textHuang, Rui. Volmer-Weber Growth of Nanoscale Self-Assembled Quantum Dots. Office of Scientific and Technical Information (OSTI), August 2009. http://dx.doi.org/10.2172/1054166.
Full textHwang, Robert Q., Carol S. Ashley, C. Jeffrey Brinker, Christine Charlotte Mitchell, Michael Ewald Bartram, and Michael Elliott Coltrin. Self-Assembled Templates for Fabricating Novel Nano-Arrays and Controlling Materials Growth. Office of Scientific and Technical Information (OSTI), February 2002. http://dx.doi.org/10.2172/794247.
Full textDye, R. C., R. E. Hermes, M. G. Martinez, and N. M. Peachey. Inorganic-organic composite nanoengineered films using self-assembled monolayers for directed zeolite film growth. Office of Scientific and Technical Information (OSTI), October 1997. http://dx.doi.org/10.2172/534511.
Full textThomson, T. Silicide formation and particle size growth in high temperature annealed, self-assembled FePt nanoparticle arrays. Office of Scientific and Technical Information (OSTI), October 2003. http://dx.doi.org/10.2172/826528.
Full textCURRO, JOHN G., JOHN DWANE MCCOY, AMALIE L. FRISCHKNECHT, and KUI YU. Molecular Self-Assembly. Office of Scientific and Technical Information (OSTI), November 2001. http://dx.doi.org/10.2172/789581.
Full textLavin, Judith, Richard Alan Kemp, and Constantine A. Stewart. Photovoltaic self-assembly. Office of Scientific and Technical Information (OSTI), October 2010. http://dx.doi.org/10.2172/1011215.
Full textFurst, Eric M. Directed Self-Assembly of Nanodispersions. Office of Scientific and Technical Information (OSTI), November 2013. http://dx.doi.org/10.2172/1105006.
Full textDe Yoreo, J., W. D. Wilson, and T. Palmore. Solvent mediated self-assembly of solids. Office of Scientific and Technical Information (OSTI), December 1997. http://dx.doi.org/10.2172/674420.
Full textCheng, Shengfeng, Steven James Plimpton, Jeremy B. Lechman, and Gary Stephen Grest. Drying/self-assembly of nanoparticle suspensions. Office of Scientific and Technical Information (OSTI), October 2010. http://dx.doi.org/10.2172/993324.
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