Electroless Deposition and Patterning of Morphologically Complex Precious Metal Films on Semiconductor Surfaces

2002 ◽  
Vol 737 ◽  
Author(s):  
Lon A. Porter ◽  
Hee Cheul Choi ◽  
Alexander E. Ribbe ◽  
Jillian M. Buriak

ABSTRACTPrecious metals are choice materials for a myriad of applications due their high electrical conductivity, resistance to corrosion, and ligand binding specificity. Indispensable in modern electronics fabrication, precious metals also enjoy widespread use as catalysts, support substrates, and sensor elements. Recent progress towards metallization on diminishing size regimes has imposed increasingly stringent demands upon thin film preparation methodologies. Metallization techniques employed in ultra large scale integration (ULSI) device fabrication, nanoelectromechanical systems (NEMS), and arrayed nanosensors will require unparalleled control of surface morphology, deposition rate, and substrate adhesion without sacrificing throughput or cost effectiveness. Furthermore, precious metal films of this type are essential for fundamental investigations aimed at elucidating the intricate nature of interfacial topics ranging from self-assembled monolayers (SAMs) to heterogeneous catalysis. In contrast to complex and expensive vacuum methods of metallization, research in our laboratory has focused on the preparation of precious metal thin films on semiconductor substrates via electroless deposition. Thin and thick films of gold, platinum, and palladium nanoparticles have been prepared as a result of the immersion of germanium and gallium arsenide substrates into dilute, aqueous solutions of tetrachloraurate (III), tetrachloroplatinate (II), and tetrachloropalladate (II), respectively. This methodology yields nanostructured precious metal films with control over surface morphology and deposition rate. Moreover, metal films prepared in this manner exhibit excellent adhesion to the underlying semiconductor substrate. The resultant films were characterized utilizing scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and scanning probe microscopy (SPM). This method provides for the facile interfacing of metal nanostructures with group (IV) and III-IV compound semiconductor surfaces.

2002 ◽  
Vol 737 ◽  
Author(s):  
Lon A. Porter ◽  
Hee Cheul Choi ◽  
J. M. Schmeltzer ◽  
Alexander E. Ribbe ◽  
Jillian M. Buriak

ABSTRACTCurrently, there is considerable interest in producing patterned metallic structures with reduced dimensions for use in technologies such as ultra large scale integration (ULSI) device fabrication, nanoelectromechanical systems (NEMS), and arrayed nanosensors, without sacrificing throughput or cost effectiveness. Research in our laboratory has focused on the preparation of precious metal thin films on semiconductor substrates via electroless deposition. This method provides for the facile interfacing of metal nanoparticles with a group (IV) and III-IV compound semiconductor surfaces. Morphologically complex films composed of gold, platinum, and palladium nanoparticles have been prepared as a result of the immersion of germanium and gallium arsenide substrates into dilute, aqueous solutions of tetrachloraurate (III), tetrachloroplatinate (II), and tetrachloropalladate (II), respectively. Continuous metallic films form spontaneously under ambient conditions, in the absence of a fluoride source or an externally applied current. This facile electroless deposition methodology provides an alternative to complex and expensive vacuum methods of metallization, yet allows for the preparation of both thin and thick nanostructured films with control over surface morphology and deposition rate. Furthermore, precious metal films prepared in this way exhibit excellent adhesion to the underlying semiconductor substrate. The resultant films were characterized utilizing scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and scanning probe microscopy (SPM). In order to apply this novel metallization method toward the development of useful technologies, patterning utilizing photolithography, microcontact printing (μCP), and scanning probe nanolithography (SPN) has been demonstrated.


Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 354
Author(s):  
Anatoly M. Sazonov ◽  
Aleksei E. Romanovsky ◽  
Igor F. Gertner ◽  
Elena A. Zvyagina ◽  
Tatyana S. Krasnova ◽  
...  

The gold and platinum-group elements (PGE) mineralization of the Guli and Kresty intrusions was formed in the process of polyphase magmatism of the central type during the Permian and Triassic age. It is suggested that native osmium and iridium crystal nuclei were formed in the mantle at earlier high-temperature events of magma generation of the mantle substratum in the interval of 765–545 Ma and were brought by meimechite melts to the area of development of magmatic bodies. The pulsating magmatism of the later phases assisted in particle enlargement. Native gold was crystallized at a temperature of 415–200 °C at the hydrothermal-metasomatic stages of the meimechite, melilite, foidolite and carbonatite magmatism. The association of minerals of precious metals with oily, resinous and asphaltene bitumen testifies to the genetic relation of the mineralization to carbonaceous metasomatism. Identifying the carbonaceous gold and platinoid ore formation associated genetically with the parental formation of ultramafic, alkaline rocks and carbonatites is suggested.


Sensors ◽  
2018 ◽  
Vol 18 (11) ◽  
pp. 4076 ◽  
Author(s):  
June Hwang ◽  
Minyang Yang

Surface-enhanced Raman spectroscopy (SERS) is a promising analytical tool due to its label-free detection ability and superior sensitivity, which enable the detection of single molecules. Since its sensitivity is highly dependent on localized surface plasmon resonance, various methods have been applied for electric field-enhanced metal nanostructures. Despite the intensive research on practical applications of SERS, fabricating a sensitive and reproducible SERS sensor using a simple and low-cost process remains a challenge. Here, we report a simple strategy to produce a large-scale gold nanoparticle array based on laser interference lithography and the electrophoretic deposition of gold nanoparticles, generated through a pulsed laser ablation in liquid process. The fabricated gold nanoparticle array produced a sensitive, reproducible SERS signal, which allowed Rhodamine 6G to be detected at a concentration as low as 10−8 M, with an enhancement factor of 1.25 × 105. This advantageous fabrication strategy is expected to enable practical SERS applications.


2019 ◽  
Author(s):  
Sasan V. Grayli ◽  
Xin Zhang ◽  
Dmitry Star ◽  
Gary Leach

Size, shape and crystallinity play a critical role in the wavelength-dependent optical responses and plasmonic local near-field distributions of metallic nanostructures. While their enhanced local fields can drive new and useful chemical and physical processes, the ability to fabricate shape-controlled single-crystal metal nanostructures and position them precisely on substrates for device applications represents a significant barrier to harnessing their greater potential. Here, we describe a novel electroless deposition process in the presence of anionic additives that yields additive-specific, shape-controlled, single-crystal plasmonic Au nanostructures on Ag(100) and Au(100) substrates. Deposition of Au in the presence of SO<sub>4</sub><sup>2-</sup> ions results in the formation of smooth Au(111)-faceted square pyramids that show large surface enhanced Raman responses. The use of halide additives such as Cl<sup>-</sup> and Br<sup>- </sup>that interact strongly with (100) facets produces highly textured hillock-type structures characterized by edge and screw-type dislocations (Cl<sup>-</sup>), or flat platelet-like features characterized by large area Au(100) terraces with (110) step edges (Br<sup>-</sup>). Use of additive combinations provides structures that comprise characteristics derived from each additive including new square pyramidal structures with dominant Au(110) facets (SO<sub>4</sub><sup>2-</sup>and Br<sup>-</sup>). Finally we demonstrate that this bottom-up electroless deposition process, when combined with top-down lithographic patterning methods, can be used to position shape-controlled, single-crystal Au nanostructures with precise location and orientation on surfaces. We anticipate that this approach will be employed as a powerful new tool to tune the plasmonic characteristics of nanostructures and facilitate their broader integration into device applications.


2021 ◽  
Author(s):  
M. D. Prendergast

Abstract The Kapalagulu intrusion in eastern Tanzania hosts a major, 420-m-thick, stratiform/stratabound platinum group element (PGE)-bearing sulfide zone—the Lubalisi reef—within a prominent, chromititiferous, harzburgite unit close to its stratigraphic base. Several features of the vertical base and precious metal distributions (in a composite stratigraphic section based upon two deep exploration drill holes) display similarities to those of offset-type PGE reefs that formed under the overall control of Rayleigh fractionation: (1) composite layering (at several scales) defined by systematic vertical variations of sulfide and precious metal contents and intermetallic ratios, indicating repeated cycles of PGE enrichment and depletion in the order Pd-Pt-Au-Cu, and (2) in the lower part of the reef, stratigraphic offsets of the precious metal peaks below peak sulfide (Cu) content. The form and geochemistry of the reef are consistent with overturns of basal liquid layers within a liquid layering system (i.e., stable density-driven stratification of a magma chamber), plus at least two minor inputs of parental magma during which the resident magma was recharged with sulfur and metals, and the effective depletion of precious metals in the magma midway through reef development. The Lubalisi reef differs from classic offset-type PGE reefs, however, principally because individual Pd, Pt, and Au enrichment peaks are coincident, not offset. The reef is set apart from other offset-type PGE reefs in three additional ways: (1) its association with olivine cumulates that crystallized soon after initial magma emplacement and well below the first appearance of cumulus pyroxene or plagioclase (implying attainment of sulfide saturation and precious metal enrichment without prolonged concentration of sulfur and chalcophile metals by normal magma cooling and differentiation), (2) the probable role of chromite crystallization in not only triggering sulfide segregation during reef formation but also facilitating precious metal enrichment in the early stages of reef development, and (3) its great width. The early stage of fractionation may also help explain the coincident precious metal peaks through its effect on apparent precious metal partition coefficients.


2019 ◽  
Vol 813 ◽  
pp. 37-42
Author(s):  
Amani Khaskhoussi ◽  
Luigi Calabrese ◽  
Edoardo Proverbio

Three different methods were used to obtain nature-inspired superhydrophobic surfaces on aluminum alloys: short-term treatment with boiling water, HF/HCl and HNO3/HCl concentrated solution etching. Afterwards a thin octadecylsilane film was deposited on all pre-treated surfaces. The surface morphology analysis showed that each method allow to obtain a specific dual nano/micro-structure. The corresponding water contact angles ranged from 160° to nearly 180°. The adhesion force between the water droplets and superhydrophobic surfaces were evaluated. The specimen etched with HF/HCl acid mixture solution showed the lowest adhesion. However, the boiling water treatment sample was characterized by the highest adhesion. Furthermore, the relationship between hydrophobic behavior and surface morphology was discussed compressively. In addition, the electrochemical measurements show that the different superhydrophobic surfaces have an excellent anti-corrosion performance evidencing promising results suitable to obtain large-scale nature-inspired superhydrophobic surfaces for several industrial applications.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 247
Author(s):  
Svetlana Ivanova ◽  
Marcela Martínez Tejada

Precious metal catalysis is often synonymous with diversity and versatility [...]


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