Relevant bibliographies by topics / Solid Gold 1

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Solid Gold 1'

Author: Grafiati
Published: 24 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Solid Gold 1"

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Liu, Liping, Jinglin Kong, Xiao Xie, Hongwen Wu, Xiaofeng Ye, Zhiliang Zhao, Lei Wang, and Quanjun Liu. "Gold nanorod translocation through a solid-state nanopore." Chinese Science Bulletin 59, no. 7 (January 29, 2014): 598–605. http://dx.doi.org/10.1007/s11434-013-0109-1.

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Xiao-Guang, Ma, Sun Wei-Guo, and Cheng Yan-Song. "Theoretical Studies on Photoionization Cross Sections of Solid Gold." Communications in Theoretical Physics 43, no. 1 (January 2005): 159–64. http://dx.doi.org/10.1088/0253-6102/43/1/030.

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Jones, Peter G., and Birte Ahrens. "Gold(I)-Komplexe mit Aminliganden, II. (Methylpyridin)-Komplexe von Gold(I) Gold(I) / Complexes with Amine Ligands, II. Methylpyridine Complexes of Gold(I)." Zeitschrift für Naturforschung B 53, no. 7 (July 1, 1998): 653–62. http://dx.doi.org/10.1515/znb-1998-0702.

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Abstract Gold(I) complexes of overall formula LAuCl (L = various methylpyridines) are non-conducting in acetone. X-ray structure analyses show that the solid state structure of the cor­ responding complex 1 (L = 2-picoline) is molecular; the 3-picoline derivative 2 is however ionic (L2Au)+(AuCl2)-. 3-Picoline forms a molecular complex LAuC6F5 (3) and also the ionic (L2Au)+(SbF6)- (4). Complexes 1, 2 and 4 display short Au ··· Au contacts, leading to chains of gold atoms; additionally, complexes 3 and 4 show weak Au ··· F contacts. The (3-picoline)-gold(III) complex trans-(L2AuCl2)+(SbF6)- (5) was obtained as a by-product; it too contains short Au ··· F contacts.
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Rösner, H., O. Kuhlmann, and E. Nembach. "Dislocation configurations in ordered copper–10 at.% gold solid solutions." Materials Science and Engineering: A 242, no. 1-2 (February 1998): 296–98. http://dx.doi.org/10.1016/s0921-5093(97)00721-1.

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Donatan, Senem, Mehmet Sarikaya, Candan Tamerler, and Mustafa Urgen. "Effect of solid surface charge on the binding behaviour of a metal-binding peptide." Journal of The Royal Society Interface 9, no. 75 (April 4, 2012): 2688–95. http://dx.doi.org/10.1098/rsif.2012.0060.

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Over the last decade, solid-binding peptides have been increasingly used as molecular building blocks coupling bio- and nanotechnology. Despite considerable research being invested in this field, the effects of many surface-related parameters that define the binding of peptide to solids are still unknown. In the quest to control biological molecules at solid interfaces and, thereby, tailoring the binding characteristics of the peptides, the use of surface charge of the solid surface may probably play an important role, which then can be used as a potential tuning parameter of peptide adsorption. Here, we report quantitative investigation on the viscoelastic properties and binding kinetics of an engineered gold-binding peptide, 3RGBP 1, adsorbed onto the gold surface at different surface charge densities. The experiments were performed in aqueous solutions using an electrochemical dissipative quartz crystal microbalance system. Hydrodynamic mass, hydration state and surface coverage of the adsorbed peptide films were determined as a function of surface charge density of the gold metal substrate. Under each charged condition, binding of 3rGBP 1 displayed quantitative differences in terms of adsorbed peptide amount, surface coverage ratio and hydration state. Based on the intrinsically disordered structure of the peptide, we propose a possible mechanism for binding of the peptide that can be used for tuning surface adsorption in further studies. Controlled alteration of peptide binding on solid surfaces, as shown here, may provide novel methods for surface functionalization used for bioenabled processing and fabrication of future micro- and nanodevices.
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Lopatynskyi, A. M., Y. O. Malymon, V. K. Lytvyn, I. V. Mogylnyi, A. E. Rachkov, A. P. Soldatkin, and V. I. Chegel. "Solid and Hollow Gold Nanostructures for Nanomedicine: Comparison of Photothermal Properties." Plasmonics 13, no. 5 (December 23, 2017): 1659–69. http://dx.doi.org/10.1007/s11468-017-0675-1.

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Bott, Raymond C., Graham A. Bowmaker, Robbie W. Buckley, Peter C. Healy, and M. C. Senake Perera. "Synthesis, Structures and Spectroscopic Properties of 1 : 1 Complexes of Gold(I) Halides with Trimesitylphosphine." Australian Journal of Chemistry 53, no. 3 (2000): 175. http://dx.doi.org/10.1071/ch99165.

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Monomeric two-coordinate gold(I) complexes, [Au(P(mes)3)X] (P(mes)3 = tris(2,4,6-trimethylphenyl)phosphine, X = Cl, Br and I), have been prepared and characterized by single-crystal X-ray structure determinations, far-infrared spectroscopy and solution and solid-state CPMAS 31 P n.m.r. spectroscopy. X-Ray structure determinations show that crystals obtained from solutions of [NBu4] [AuX2] and P(mes)3 in acetonitrile for X = Cl, Br and I and in dimethylformamide (dmf) for X = Br and I form an isomorphous series of complexes, crystallizing in space group P21/c with a ª 8, b ª 22, c ª 13 Å, b ª 98˚ (a form). Crystallization of the chloride from dimethylformamide yields the solvated complex [Au(P(mes)3)X]·(dmf) in space group P2/a with a 15.224(2), b 10.070(1), c 18.210(4) Å, b 100.42(2)˚. Electrochemical synthesis of the complexes for X = Cl and Br yield two new crystalline phases; the chloride in space group P21/c with a 10.249(2), b 8.189(2), c 31.844(3) Å, b 91.68(1)˚ (b form) and the bromide in space group Pbca with a 19.208(4), b 15.586(3), c 16.962(4) Å ( g form). The Au–P bond lengths increase in the order Cl < Br < I with distances c. 0.02–0.03 Å longer than average values for other [Au(PR3)X] complexes, reflecting steric congestion by the P(mes)3 ligand. For the unsolvated complexes, the Au–X distances are c. 0.02 Å shorter than average values. For the Cl/dmf solvate, both Au–P and Au–X bond lengths increase. For the a complexes, far-infrared spectra show n(Au 35,37 Cl) 336, 329 cm –1 , n(AuBr) 234 cm –1 and n(AuI) 195 cm –1 and solid-state 31 P CPMAS n.m.r. spectra yield broad peaks with d–3.9 (Cl), –0.6 (Br) and +6.0 I). For the Cl/dmf solvate, n(Au 35,37 Cl) are 334, 327 cm –1 and d is –4.4. Solution 31 P n.m.r. spectra in CDCl3 give sharp single peaks at d –5.0 (Cl), –1.4 (Br) and +5.5 (I) with the similarity of the values with those for the solid-state spectra consistent with similar conformational structures for the [Au(P(mes)3)X] molecules in the two states.
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Adlim, Adlim, and Mohamad Abu Bakar. "PREPARATION OF CHITOSAN-GOLD NANOPARTICLES: PART 2. THE ROLE OF CHITOSAN." Indonesian Journal of Chemistry 8, no. 3 (June 17, 2010): 320–26. http://dx.doi.org/10.22146/ijc.21585.

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Colloidal gold nanoparticles prepared by employing chitosan as the stabilizer in solvent of methanol-acetic acid solution were stable for months without precipitation. The mole ratio of chitosan-gold ions of 5:1 - 30:1 gave dispersed and fine gold particles in range of 9.4-10.4 nm. Gold reduction in chitosan matrix was faster at higher chitosan concentration, and molar ratio of chi : Au, from 5:1 to 40:1. Higher acidity of acetic acid (pH 2-6) led to faster reduction of gold ions. The intensity of gold metal colloid plasmon band increased at higher concentration of acetic acid. Chitosan functioned both as a stabilizer and a reducing agent for gold ions. Gold colloidal particles immobilized on chitosan coated TiO2 as the solid support gave more dispersed and smaller particles (4.6 nm) compared with gold particles supported on TiO2 without chitosan coating. Keywords: gold nanoparticles, chitosan, chitosan coated TiO2
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Tzeng, Biing-Chiau, Johann Zank, Annette Schier, and Hubert Schmidbaur. "The Structural Chemistry of GoId(I) Quinoline-2-thiolate and Iodide Complexes of Polytertiary Phosphines." Zeitschrift für Naturforschung B 54, no. 7 (July 1, 1999): 825–31. http://dx.doi.org/10.1515/znb-1999-0701.

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Treatment of (chloro)gold(I) complexes of di- and tetra-tertiary phosphines with equivalent quantities of sodium quinoline-2-thiolate in methanol / dichloromethane affords the corresponding (phosphine)gold(I) quinoline-2-thiolates in high yields. The di- and tetranuclear complexes, respectively, of α, ω-bis(diphenylphosphino)-propane (1), -butane (2) and -pentane (3) and of tris(2-diphenylphosphino-ethyl)phosphine (4) have been obtained as crystalline solids, and the structures of 2 and 4 have been determined by single crystal X-ray diffraction studies. Unexpectedly, the molecules of 2 are loosely aggregated into strings via weak intermolecular gold-sulfur, not via Au ∙∙∙ Au interactions. Compound 4 is a monomeric tetranuclear cluster in the solid state with two intramolecular gold-gold bonds. Bis(2-diphenylphosphino-ethyl)- phenylphosphine (PPP) forms trinuclear complexes with gold(I) chloride, bromide and iodide (5a - c). The iodide complex features a chain structure through intermolecular Au ∙∙∙ Au contacts between the two terminal P-Au-I units. The closest contacts between the chains are determined by Au ∙∙∙ I and I ∙∙∙ I interactions of the central P-Au-I unit.
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Nguyen, Thuong Thi Kim, Huyen Thu Luu, Loi Duc Vu, Thao Thi Ta, and Giang Thi Huong Le. "Determination of Total Mercury in Solid Samples by Anodic Stripping Voltammetry." Journal of Chemistry 2021 (January 12, 2021): 1–8. http://dx.doi.org/10.1155/2021/8888879.

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The anodic stripping voltammetry (ASV) was investigated to determine total mercury in solid samples using a gold electrode. The mercury was deposited on the gold electrode in a preconcentration step. The oxidation peak of mercury was irreversible. The optimal conditions of the procedure were found to be as follows: 0.05 mol L−1 HCl solution, deposition potential −0.5 V vs. Ag/AgCl/KCls, deposition time 40 s, and sweep rate 0.04 V s−1. Under the optimal conditions, the peak current showed a linear dependence on Hg2+ concentration in the range from 0.01 to 0.1 mg l−1. The detection limit and quantification limit were 4.28 µg L−1 and 12.98 µg L−1, respectively. The mean recovery and relative standard deviation were 91.2% and 2.4% (n = 9). The procedure was successfully applied for determining total mercury in samples collected from Hanoi light bulb warehouse—The Rang Dong Light Source and Vacuum Flask JSC. The results were compared with cold vapor atomic absorption spectrometry (CV-AAS).
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Dissertations / Theses on the topic "Solid Gold 1"

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Calais, Linus. "The Representation of Culture : A Comparative Analysis of Cultural Representation in Swedish EFL Coursebooks." Thesis, Jönköping University, HLK, Ämnesforskning, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-53604.

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The overall aim of this study is to analyse the cultural representation in fictional texts in three English as a Foreign Language (EFL) coursebooks written for the English 5 course in Swedish upper secondary school. The three coursebooks are Blueprint A 3.0, Pick & Mix 1, and Solid Gold 1. The study was conducted in order to compare and discuss the portrayal and representation of cultures of the English-speaking world. The method used consists of a combination of the two-stage model constructed by McDonough et al. (2013) and a qualitative content analysis. The three coursebooks were analysed through the theoretical framework of postcolonial theory. The results show that American culture is represented to a higher extent than any other culture in the included fictional works. Because of the discrepancy in representation, American culture was portrayed through various societal issues, living conditions, and cultural features. However, many other cultures of the English-speaking world were barely represented at all. Furthermore, the results show that cultures such as Indian or Irish are not included in all the coursebooks. The lack of fictional texts representing cultures of Africa included in the coursebooks further shows the discrepancy and specific focus on certain parts of the English-speaking world. Solid Gold 1 was the only one of the three coursebooks which included fictional texts discussing all cultures highlighted. Although there is a notable difference in the representation of cultures, and the number of times certain cultures are mentioned, the analysis shows that the coursebooks create many opportunities, through fictional texts, for students to learn about societal issues, cultural features, and living conditions in parts of the world where English is used, meeting the requirements of the Swedish curriculum.
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Harris, Kristopher J. "Solid-state spin-1/2 NMR studies of disorder, bonding, and symmetry." Phd thesis, 2009. http://hdl.handle.net/10048/429.

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This thesis is concerned with applications of modern solid-state NMR spectroscopy. Investigations of three quite different types are undertaken, each of which attempt to advance knowledge in the fields of chemistry and NMR. The goal of each project is to obtain insight into the effects of chemical environment, in particular bonding, on the NMR observables. Carbon-13 and nitrogen-15 solid-state nuclear magnetic resonance has been used to study solid samples containing the dicyanoaurate(I) anion, [Au(CN)2]-, with n-butylammonium, potassium, and thallium counterions. Differences in Au-Tl metallophilic bonding are shown to cause a difference in the isotropic cyanide carbon-13 chemical shift of up to 15.7 ppm, while differences in Au-Au aurophilic bonding are found to be responsible for a change of up to 5.9 ppm. Disordered polymeric gold(I) monocyanide was also investigated, and a range of 7+-2% to 25+-5% of the AuCN chains are found to be "slipped" instead of aligned with the neighbouring chains at the metal position. An investigation of the chemical shift tensors of the 13C-labelled carbons in solid samples of Ph13C≡13CPh and (η2-Ph13C≡13CPh)Pt(PPh3)2·(C6H6) has also been carried out. Coordination of diphenylacetylene to platinum causes a change in the 13C chemical shift tensor orientation and a net increase in the isotropic chemical shift. The carbon chemical shift tensors in the platinum complex bear a striking similarity to those of the alkenyl-carbons in trans-Ph(H)C=C(H)Ph, and a theoretical discussion of these observations is presented. Each of the fundamental NMR interaction tensors (σ, J, D and V) may be decomposed into isotropic, symmetric, and antisymmetric components. Observations of all theoretically allowed components other than the antisymmetric portion of J (Janti) have previously been published. Andrew and Farnell's theory (Mol. Phys. 15, 157 (1968)) for the effects of Janti on NMR spectra has been extended to powdered samples, and methods for analyzing the resultant line shapes have been determined. Finally, the first reported experimental attempts to measure Janti are presented, and experimental proof that no elements of Janti(119Sn,119Sn) in hexa(p-tolyl)ditin are larger than 2900 Hz is given.
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Books on the topic "Solid Gold 1"

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Arshed, Norin, Julie McFarlane, and Robert MacIntosh, eds. Enterprise and its Business Environment. Goodfellow Publishers, 2016. http://dx.doi.org/10.23912/978-1-910158-78-4-2852.

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A clear and insightful introduction to the world of business enterprise and the inner workings of the firm. It explores the role of entrepreneurs, consumers and businesses to understand how their roles affect the production and allocation of good and services and provides a solid base from which those new to the study of business can develop their own interests in relation to the most powerful economic and entrepreneurial forces shaping the world in which we live.
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Book chapters on the topic "Solid Gold 1"

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Joseph, Ryan. "Solid Foods Aren’t Good for You." In HIV-Negative, 181–90. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-6106-8_17.

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Robinson, Garry. "Providing a Solid Foundation with Good Programming Practices." In Real World Microsoft Access Database Protection and Security, 81–107. Berkeley, CA: Apress, 2004. http://dx.doi.org/10.1007/978-1-4302-0793-1_4.

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Desai, T., H. Daido, M. Suzuk, N. Sakaya, Ariel R. Guerreiro, and K. Mima. "X-Ray Emission from Laser Irradiated Structured Gold Targets." In Atoms, Solids, and Plasmas in Super-Intense Laser Fields, 381–87. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1351-3_24.

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Zhang, Hong, Shui Yuan Chen, Su Zhen Tang, Wen Pao Ke, Heng Lai, and Zhi Gao Huang. "Electrical Conductivity and Low-Field Magnetoresistance in La2/3(Ca0.60Ba0.40)1/3Mn1-xVxO3 Prepared by Sol-Gol." In Solid State Phenomena, 901–4. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-30-2.901.

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Denisoff, R. Serge. "What is Popular Music: A Silly Question?" In Solid Gold, 1–43. Routledge, 2020. http://dx.doi.org/10.4324/9780429338663-1.

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Mruk, Christopher J. "What Is Authentic Self-Esteem and Why Does It Matter?" In Feeling Good by Doing Good, 1–26. Oxford University Press, 2018. http://dx.doi.org/10.1093/med-psych/9780190637163.003.0001.

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Chapter 1 deals with the crucial issue of defining self-esteem to set solid foundations for the rest of the book. The chapter describes all three major ways that social scientists, mental health professionals, and people in general define self-esteem. Then this section shows how defining self-esteem in terms of a relationship between competence and worthiness is best for two reasons. First, this approach reflects John Milton’s original use of the term, which bases self-esteem on doing that which is just and right rather than simply on feeling good about oneself. Second, this definition gives people a sense of where to go when facing life’s challenges and how to make healthier decisions. The chapter includes a description of the basic types of self-esteem, namely, low, defensive, and authentic self-esteem, and various self-esteem related problems.
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Van der Westhuizen, Thea. "Good Entrepreneurial Intentions, No Entrepreneurial Action." In Handbook of Research on Entrepreneurship, Innovation, and Internationalization, 207–29. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-8479-7.ch008.

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Against the background of the extremely high youth unemployment rate in South Africa, a survey was conducted among final-year undergraduate business students, asking them to rate the importance of five entrepreneurial processes: 1) obtaining entrepreneurship-related education, 2) searching, 3) planning, 4) marshalling, 5) implementing. Responses indicated that they recognized the importance of all five and also displayed personality traits positively related to individual entrepreneurial orientation and entrepreneurial intent. Continuing deterioration in youth employment nonetheless suggests that good entrepreneurial intentions do not translate into sustainable entrepreneurial action. Respondents failed to recognize the importance of their lecturers' role in their business education and seemed not to perceive that they needed intensive support from their lecturers to become entrepreneurial. They also failed to recognize the crucial importance of solid ground-work before starting a new business. These gaps in knowledge have an important bearing on the high unemployment rate.
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Van der Westhuizen, Thea. "Good Entrepreneurial Intentions, No Entrepreneurial Action." In Research Anthology on Business and Technical Education in the Information Era, 1124–46. IGI Global, 2021. http://dx.doi.org/10.4018/978-1-7998-5345-9.ch063.

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Against the background of the extremely high youth unemployment rate in South Africa, a survey was conducted among final-year undergraduate business students, asking them to rate the importance of five entrepreneurial processes: 1) obtaining entrepreneurship-related education, 2) searching, 3) planning, 4) marshalling, 5) implementing. Responses indicated that they recognized the importance of all five and also displayed personality traits positively related to individual entrepreneurial orientation and entrepreneurial intent. Continuing deterioration in youth employment nonetheless suggests that good entrepreneurial intentions do not translate into sustainable entrepreneurial action. Respondents failed to recognize the importance of their lecturers' role in their business education and seemed not to perceive that they needed intensive support from their lecturers to become entrepreneurial. They also failed to recognize the crucial importance of solid ground-work before starting a new business. These gaps in knowledge have an important bearing on the high unemployment rate.
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Ponelis, Shana. "Information as Economic Good." In Advances in Business Information Systems and Analytics, 1–13. IGI Global, 2014. http://dx.doi.org/10.4018/978-1-4666-4983-5.ch001.

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Information plays an important role in most economies, and in some economies constitutes the dominant sector where information is created, traded, sold, and brokered as a commodity or economic good. It is therefore important for all stakeholders to understand the unique nature of information as an economic good and the implications thereof on the creation, trading, selling, and brokering thereof, as well as the potential legal and ethical issues. The purpose of this chapter is to provide the reader with an overview of the origins of the information economy, information as an economic good, and the characteristics that distinguish it from other economic goods; the impact of these characteristics on the pricing and packaging of information goods as well as some of the legal and ethical issues that pertain to information systems are highlighted. The chapter concludes with possible future trends and research directions.
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Enoki, Toshiaki, Morinobu Endo, and Masatsugu Suzuki. "Synthesis and Intercalation Chemistry." In Graphite Intercalation Compounds and Applications. Oxford University Press, 2003. http://dx.doi.org/10.1093/oso/9780195128277.003.0004.

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Alkali metal GICs are the best known donor type GICs, since they are easily prepared and their brilliant gold color for stage-1 GICs has attracted scientists working in intercalation chemistry. They have therefore been targets of intensive and detailed studies of their solid-state properties on the basis of the employment of highly oriented pyrolytic graphite (HOPG). There are several intercalation methods, which are classified basically into vapor-phase reaction, reaction of the mixture of graphite and alkali metal, high pressure reaction, electrochemical reaction, and reaction in a solvent. Among these methods, vapor-phase intercalation reaction is the most popular. The two-zone method can easily give alkali metal GICs with well-defined single-stage phases. The vapor pressure of the alkali metal becomes high enough to obtain a satisfactory reaction rate for intercalation reaction in the temperature range 200-550°C, at which we can use a Pyrex glass tube as a reaction chamber. Figure 2.1 shows a typical two-zone method, where graphite and alkali metal are maintained at different temperatures, TG and TI, respectively, in a vacuum-sealed glass tube placed in a two-zone furnace. Changing TI controls the vapor pressure of the alkali metal. Figure 2.2 presents the conditions of intercalation reaction with potassium, where single-stage phase samples with stages 1 to 8 are obtained by changing the temperature difference TG — TK (Nishitani et al., 1983). Typical experimental conditions are given in Table 2.1 for the preparation of K, Rb, and Cs GICs (Dresselhaus and Dresselhaus, 1981). The intercalation reaction is again carried out by heating a mixture of graphite and alkali metal in a vacuum-sealed glass tube. In this case, the reaction becomes considerably more rapid owing to direct contact of molten alkali metal with graphite, although the reaction takes place in a similar manner to the vapor-phase reaction. A stainless steel tube is used for the intercalation of lithium since lithium vapor degrades a glass tube because of its high chemical activity. Alkali metal can be intercalated into graphite when the alkali metal is solvated in liquid ammonia or an organic solvent such as dimethylsulphoxide (DMSO).
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Conference papers on the topic "Solid Gold 1"

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Baylam, I., O. Balci, N. Kakenov, C. Kocabas, and A. Sennaroglu. "Graphene-Gold Supercapacitor As a Voltage-Controlled Saturable Absorber for Femtosecond Pulse Generation." In Advanced Solid State Lasers. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/assl.2015.aw1a.1.

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Yoshiba, M., C. Y. Chen, T. F. M. Chang, D. Yamane, K. Machida, K. Masu, and M. Sone. "Mechanical Properties of Electrodeposited Gold for MEMS Device." In 2015 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2015. http://dx.doi.org/10.7567/ssdm.2015.ps-2-1.

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Fujita, K., K. Yasui, M. Ozawa, K. Odoi, and H. Ichikawa. "Organic resistive memory device composed of hyperbranched polystyrene and gold nanoparticles." In 2011 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2011. http://dx.doi.org/10.7567/ssdm.2011.b-4-1.

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Lin, C. T., P. W. Huang, J. C. Wang, L. C. Chang, C. H. Chen, Y. Y. Chen, and C. S. Lai. "Performance Revelation and Optimization of Gold Nanocrystal for Future Nonvolatile Memory Application." In 2012 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2012. http://dx.doi.org/10.7567/ssdm.2012.g-1-4.

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Ichikawa, H., K. Yasui, M. Ozawa, and K. Fujita. "Improvement in Repeatability for Organic Bistable Device using Hyper-Branched Polymer / Gold Nanoparticles Composite." In 2008 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2008. http://dx.doi.org/10.7567/ssdm.2008.i-1-2.

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Sugawa, K., T. Kawahara, T. Akiyama, and S. Yamada. "Facile Fabrication of Densely Packed Multistructure Assemblies of Gold Nanoparticles using Layer-by-layer Method." In 2008 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2008. http://dx.doi.org/10.7567/ssdm.2008.f-1-6.

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Arulkumaran, S., G. I. Ng, K. Ranjan, C. M. Manoj Kumar, S. C. Foo, K. S. Ang, and S. Vicknesh. "Record-Low Contact Resistance for InAlN/AlN/GaN HEMTs on Si with Non-Gold Metal." In 2014 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2014. http://dx.doi.org/10.7567/ssdm.2014.e-1-6l.

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Arakawa, Taichi, Tomoaki Kawahara, Tsuyoshi Akiyama, and Sunao Yamada. "Facile Fabrication of Gold Nanoparticle-Titanium Oxide Alternate Assemblies by Surface Sol-Gel Process and Their Photoresponsive Properties." In 2006 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2006. http://dx.doi.org/10.7567/ssdm.2006.i-1-5.

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Fujii, Y., T. Shimizu, M. Hosoda, G. Wu, S. Huang, H. Sakaue, T. Takahagi, and S. Shingubara. "Large Negative Resistance Property Observed in 3-D Network of DNA and Gold Nanoparticle Formed by DNA Mediated Self-organization." In 2004 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2004. http://dx.doi.org/10.7567/ssdm.2004.h-1-4.

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Sun, Liyong, Jun Zhou, and Phil Jones. "Effect of Nanostructures and Wettability on the Instability of Thin Water Films on a Solid Surface: A Molecular Dynamics Study." In ASME 2016 14th International Conference on Nanochannels, Microchannels, and Minichannels collocated with the ASME 2016 Heat Transfer Summer Conference and the ASME 2016 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icnmm2016-7921.

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Abstract:
Molecular dynamics simulations are performed to investigate the stability of thin water films on square gold nanostructures of varying depth and wavelength. The critical film thickness of breakup is shown to increase linearly with nanostructure depth, and is not affected by nanostructure wavelength. In addition, the wettability of the gold surface is controlled from superhydrophilic to hydrophobic by altering the energy parameter of the solid-liquid potential, and the equilibrium contact angle for each energy parameter is calculated using a droplet spreading simulation. Four different energy parameters of the solid-liquid potential are investigated. The ratio of the energy parameter to the energy parameter of water and gold is 1, 0.5, 0.25 and 0.1. The case for ratio of 1 represents water on superhydrophilic gold surfaces. The relationship between the critical film thickness of breakup and the equilibrium contact angle is demonstrated. The results of the present work will provide guidelines for nanostructure design for controlling thin film stability.
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