40 research outputs found
Deep Etching of Single- and Polycrystalline Silicon with High Speed, High Aspect Ratio, High Uniformity, and 3D Complexity by Electric Bias-Attenuated Metal-Assisted Chemical Etching (EMaCE)
In this work, a novel wet silicon
(Si) etching method, electric bias-attenuated metal-assisted chemical
etching (EMaCE), is demonstrated to be readily available for three-dimensional
(3D) electronic integration, microelectromechinal systems, and a broad
range of 3D electronic components with low cost. On the basis of the
traditional metal-assisted chemical etching process, an electric bias
was applied to the Si substrate in EMaCE. The 3D geometry of the etching
profile was effectively controlled by the bias in a real-time manner.
The reported method successfully fabricated an array of over 10 000
vertical holes with diameters of 28 μm on 1 cm<sup>2</sup> silicon
chips at a rate of up to 11 μm/min. The sidewall roughness was
kept below 50 nm, and a high aspect ratio of over 10:1 was achieved.
The 3D geometry could be attenuated by the variable applied bias in
real time. Vertical deep etching was realized on (100)-, (111)-Si,
and polycrystalline Si substrates. Complex features with lateral dimensions
of 0.8–500 μm were also fabricated with submicron accuracy
Nano Ag-Deposited BaTiO<sub>3</sub> Hybrid Particles as Fillers for Polymeric Dielectric Composites: Toward High Dielectric Constant and Suppressed Loss
Nano Ag-deposited BaTiO<sub>3</sub> (BT-Ag) hybrid particles usable as fillers for flexible polymeric
composites to obtain high dielectric constant, low conductivity, and
low dielectric loss were developed. BT-Ag hybrid particles were synthesized
via a seed-mediated growing process by a redox reaction between silver
nitrate and ethylene glycol. Nano Ag particles with a size less than
20 nm were discretely grown on the surface of the 100 nm BaTiO<sub>3</sub>. The similar lattice spacing of the (1 1 1) planes of BT
and Ag led to the hetero-epitaxial growth of Ag on the BT surface.
The thickness of the coherent interface was about 3 nm. The adhesion
of Ag to BT efficiently prevented the continuous contact between Ag
particles in the polyvinylidene fluoride (PVDF) matrix and suppressed
the formation of the conducting path in the composite. As a result,
with a filler loading of 43.4 vol %, the composite exhibited a dielectric
constant (<i>D</i><sub>k</sub>) value of 94.3 and dielectric
loss (tan δ) of 0.06 at 1 kHz. An even higher <i>D</i><sub>k</sub> value of 160 at 1 kHz (16 times larger than that of
PVDF) was obtained when the content of BT-Ag was further increased,
with low conductivity (σ < 10<sup>–5</sup> S m<sup>–1</sup>) and low dielectric loss (tan δ = 0.11), demonstrating
promising applications in the electronic devices
Highly Thermally Conductive Composite Papers Prepared Based on the Thought of Bioinspired Engineering
The rapid development
of modern electronics and three-dimensional integration sets stringent
requirements for efficient heat removal of thermal-management materials
to ensure the long lifetime of the electronics. However, conventional
polymer composites that have been used widely as thermal-management
materials suffer from undesired thermal conductivity lower than 10
W m<sup>–1</sup> K<sup>–1</sup>. In this work, we report
a novel thermally conductive composite paper based on the thought
of bioinspired engineering. The advantage of the bioinspired papers
over conventional composites lies in that they possess a very high
in-plane thermal conductivity up to 21.7 W m<sup>–1</sup> K<sup>–1</sup> along with good mechanical properties and high electrical
insulation. We attribute the high thermal conductivity to the improved
interfacial interaction between assembled components through the introduction
of silver nanoparticles and the oriented structure based on boron
nitride nanosheets and silicon carbide nanowires. This thought based
on bioinspired engineering provides a creative opportunity for design
and fabrication of novel thermally conductive materials, and this
kind of composite paper has potential applications in powerful integrated
microelectronics
Facile Preparation of Superelastic and Ultralow Dielectric Boron Nitride Nanosheet Aerogels via Freeze-Casting Process
As a structural analogue of graphene,
boron nitride nanosheets
(BNNSs) have attracted ever-growing research interest in the past
few years, due to their remarkably mechanical, electrical, and thermal
properties. The preparation of BNNS aerogels is considered to be one
of the most effective approaches for their practical applications.
However, it has remained a great challenge to fabricate BNNS aerogels
with superelasticity by a facile method. Here, we report the preparation
of BNNS aerogels via a facile method involving polymer-assisted cross-linking
and freeze-casting strategies. The resulting aerogels exhibit a well-ordered
and anisotropic microstructure, leading to anisotropic superelasticity,
high compressive strength, and excellent energy absorption ability.
The unique microstructure also endows the aerogels with ultralow dielectric
constant (1.24) and loss (∼0.003). The successful fabrication
of such fascinating materials paves the way for application of BNNSs
in energy-absorbing services, catalyst carrier, and environmental
remediation, etc
Pressure-Induced Oriented Attachment Growth of Large-Size Crystals for Constructing 3D Ordered Superstructures
Oriented attachment (OA), a nonclassical
crystal growth mechanism,
provides a powerful bottom-up approach to obtain ordered superstructures,
which also demonstrate exciting charge transmission characteristic.
However, there is little work observably pronouncing the achievement
of 3D OA growth of crystallites with large size (<i>e.g.</i>, submicrometer crystals). Here, we report that SnO<sub>2</sub> 3D
ordered superstructures can be synthesized by means of a self-limited
assembly assisted by OA in a designed high-pressure solvothermal system.
The size of primary building blocks is 200–250 nm, which is
significantly larger than that in previous results (normally <10
nm). High pressure plays the key role in the formation of 3D configuration
and fusion of adjacent crystals. Furthermore, this high-pressure strategy
can be readily expanded to additional materials. We anticipate that
the welded structures will constitute an ideal system with relevance
to applications in optical responses, lithium ion battery, solar cells,
and chemical sensing
Facile Preparation of Superelastic and Ultralow Dielectric Boron Nitride Nanosheet Aerogels via Freeze-Casting Process
As a structural analogue of graphene,
boron nitride nanosheets
(BNNSs) have attracted ever-growing research interest in the past
few years, due to their remarkably mechanical, electrical, and thermal
properties. The preparation of BNNS aerogels is considered to be one
of the most effective approaches for their practical applications.
However, it has remained a great challenge to fabricate BNNS aerogels
with superelasticity by a facile method. Here, we report the preparation
of BNNS aerogels via a facile method involving polymer-assisted cross-linking
and freeze-casting strategies. The resulting aerogels exhibit a well-ordered
and anisotropic microstructure, leading to anisotropic superelasticity,
high compressive strength, and excellent energy absorption ability.
The unique microstructure also endows the aerogels with ultralow dielectric
constant (1.24) and loss (∼0.003). The successful fabrication
of such fascinating materials paves the way for application of BNNSs
in energy-absorbing services, catalyst carrier, and environmental
remediation, etc
Vertically Aligned and Interconnected SiC Nanowire Networks Leading to Significantly Enhanced Thermal Conductivity of Polymer Composites
Efficient heat removal
via thermal management materials has become one of the most critical
challenges in the development of modern microelectronic devices. However,
previously reported polymer composites exhibit limited enhancement
of thermal conductivity, even when highly loaded with thermally conductive
fillers, because of the lack of efficient heat transfer pathways.
Herein, we report vertically aligned and interconnected SiC nanowire
(SiCNW) networks as efficient fillers for polymer composites, achieving
significantly enhanced thermal conductivity. The SiCNW networks are
produced by freeze-casting nanowire aqueous suspensions followed by
thermal sintering to consolidate the nanowire junctions, exhibiting
a hierarchical architecture in which honeycomb-like SiCNW layers are
aligned. The composite obtained by infiltrating SiCNW networks with
epoxy resin, at a relatively low SiCNW loading of 2.17 vol %, represents
a high through-plane thermal conductivity (1.67 W m<sup>–1</sup> K<sup>–1</sup>) compared to the pure matrix, which is equivalent
to a significant enhancement of 406.6% per 1 vol % loading. The orderly
SiCNW network which can act as a macroscopic expressway for phonon
transport is believed to be the main contributor for the excellent
thermal performance. This strategy provides insights for the design
of high-performance composites with potential to be used in advanced
thermal management materials
Room-Temperature Nanowelding of a Silver Nanowire Network Triggered by Hydrogen Chloride Vapor for Flexible Transparent Conductive Films
High contact resistance between silver
nanowires (AgNWs) is a key issue in widespread application of AgNW
flexible transparent conductive films as a promising candidate to
replace the brittle and expensive indium tin oxide. A facile, room-temperature
nanowelding method of an AgNW network triggered by hydrogen chloride
(HCl) vapor is demonstrated to reduce the sheet resistance of the
AgNW network. Under the visible light, O<sub>2</sub> and HCl vapor
serving as an etching couple induced silver atoms to be transferred
from the bottom AgNW at the junction to the top one, and then, these
silver atoms epitaxially recrystallized at the contact position with
the lattice of the top AgNW as the template, ultimately resulting
in the coalescence of the junction between AgNWs. Polydimethylsiloxane
(PDMS) was spin-coated onto the HCl-vapor-treated (HVT) AgNW network
on the polyethylene terephthalate substrate to fabricate PDMS/HVT
AgNW films. The fabricated film with low sheet resistance and high
transmittance retained its conductivity after 4000 bending cycles.
Furthermore, excellent heating performance, electromagnetic interference
shielding effectiveness, and foldability were obtained in the PDMS/HVT
AgNW film. Thus, the role of the simple nanowelding process is evident
in enhancing the performance of AgNW transparent conductive films
for emerging soft optoelectronic applications