scholarly journals Phase-transition–induced p-n junction in single halide perovskite nanowire

2018 ◽  
Vol 115 (36) ◽  
pp. 8889-8894 ◽  
Author(s):  
Qiao Kong ◽  
Woochul Lee ◽  
Minliang Lai ◽  
Connor G. Bischak ◽  
Guoping Gao ◽  
...  
Keyword(s):  
Phase Transition ◽  
Building Blocks ◽  
Chemical Doping ◽  
New Class ◽  
Anion Vacancies ◽  
Cation And Anion Vacancies ◽  
Halide Perovskite ◽  
Two Phases ◽  
P Type ◽  
Formation Energies

Semiconductor p-n junctions are fundamental building blocks for modern optical and electronic devices. The p- and n-type regions are typically created by chemical doping process. Here we show that in the new class of halide perovskite semiconductors, the p-n junctions can be readily induced through a localized thermal-driven phase transition. We demonstrate this p-n junction formation in a single-crystalline halide perovskite CsSnI3 nanowire (NW). This material undergoes a phase transition from a double-chain yellow (Y) phase to an orthorhombic black (B) phase. The formation energies of the cation and anion vacancies in these two phases are significantly different, which leads to n- and p- type electrical characteristics for Y and B phases, respectively. Interface formation between these two phases and directional interface propagation within a single NW are directly observed under cathodoluminescence (CL) microscopy. Current rectification is demonstrated for the p-n junction formed with this localized thermal-driven phase transition.

Native Defects in Wurtzite GaN And AlN

1994 ◽  
Vol 339 ◽  
Author(s):  
P. Boguslawski ◽  
E. Briggs ◽  
T. A. White ◽  
M. G. Wensell ◽  
J. Bernholc
Keyword(s):  
Theoretical Study ◽  
Shallow Donor ◽  
Wave Functions ◽  
Quantum Molecular Dynamics ◽  
Native Defects ◽  
Anion Vacancies ◽  
Cation And Anion Vacancies ◽  
Wide Gap ◽  
Type Character ◽  
Formation Energies

AbstractThe results of an extensive theoretical study of native defects in GaN and of vacancies in AlN are presented. We have considered cation and anion vacancies, antisites, and intersti-tials. The computations were carried out using quantum molecular dynamics, in supercells containing 72 atoms. Due to the wide gap of nitrides, the formation energies of defects depend strongly on the position of the Fermi level. The N vacancy in GaN introduces a shallow donor level that may be responsible for the n-type character of as-grown GaN.Other defects introduce deep states in the gap, with strongly localized wave functions.

Void-Lattice Formation in Natural Fluorite by Electron Irradiation

1976 ◽  
Vol 34 ◽  
pp. 614-615 ◽  
Author(s):  
L.E. Murr
Keyword(s):  
Electron Microscope ◽  
Electron Irradiation ◽  
Heavy Ion ◽  
High Energy ◽  
Stoichiometric Ratio ◽  
Direct Observations ◽  
Transmission Electron ◽  
Anion Vacancies ◽  
Cation And Anion Vacancies ◽  
Lattice Formation

The production of void lattices in metals as a result of displacement damage associated with high energy and heavy ion bombardment is now well documented. More recently, Murr has shown that a void lattice can be developed in natural (colored) fluorites observed in the transmission electron microscope. These were the first observations of a void lattice in an irradiated nonmetal, and the first, direct observations of color-center aggregates. Clinard, et al. have also recently observed a void lattice (described as a high density of aligned "pores") in neutron irradiated Al2O3 and Y2O3. In this latter work, itwas pointed out that in order that a cavity be formed,a near-stoichiometric ratio of cation and anion vacancies must aggregate. It was reasoned that two other alternatives to explain the pores were cation metal colloids and highpressure anion gas bubbles.Evans has proposed that void lattices result from the presence of a pre-existing impurity lattice, and predicted that the formation of a void lattice should restrict swelling in irradiated materials because it represents a state of saturation.

A Bottom-Up Approach to Solution-Processed, Atomically Precise Graphitic Cylinders on Surfaces

2018 ◽  
Author(s):  
Erik Leonhardt ◽  
Jeff M. Van Raden ◽  
David Miller ◽  
Lev N. Zakharov ◽  
Benjamin Aleman ◽  
...  
Keyword(s):  
Self Assembly ◽  
Carbon Nanostructures ◽  
Carbon Nanomaterials ◽  
Circle Packing ◽  
Pyrolytic Graphite ◽  
Building Blocks ◽  
Bottom Up ◽  
Casting Technique ◽  
New Class ◽  
Solution Casting Technique

Extended carbon nanostructures, such as carbon nanotubes (CNTs), exhibit remarkable properties but are difficult to synthesize uniformly. Herein, we present a new class of carbon nanomaterials constructed via the bottom-up self-assembly of cylindrical, atomically-precise small molecules. Guided by supramolecular design principles and circle packing theory, we have designed and synthesized a fluorinated nanohoop that, in the solid-state, self-assembles into nanotube-like arrays with channel diameters of precisely 1.63 nm. A mild solution-casting technique is then used to construct vertical “forests” of these arrays on a highly-ordered pyrolytic graphite (HOPG) surface through epitaxial growth. Furthermore, we show that a basic property of nanohoops, fluorescence, is readily transferred to the bulk phase, implying that the properties of these materials can be directly altered via precise functionalization of their nanohoop building blocks. The strategy presented is expected to have broader applications in the development of new graphitic nanomaterials with π-rich cavities reminiscent of CNTs.

Reversible microscale assembly of nanoparticles driven by the phase transition of a thermotropic liquid crystal

2017 ◽  
Author(s):  
Niamh Mac Fhionnlaoich ◽  
Stephen Schrettl ◽  
Nicholas B. Tito ◽  
Ye Yang ◽  
Malavika Nair ◽  
...  
Keyword(s):  
Phase Transition ◽  
Liquid Crystal ◽  
Self Assembly ◽  
Nematic Phase ◽  
Hierarchical Control ◽  
Building Blocks ◽  
Model System ◽  
Microscopic Level ◽  
Reversible Process ◽  
Thermotropic Liquid Crystal

The arrangement of nanoscale building blocks into patterns with microscale periodicity is challenging to achieve via self-assembly processes. Here, we report on the phase transition-driven collective assembly of gold nanoparticles in a thermotropic liquid crystal. A temperature-induced transition from the isotropic to the nematic phase leads to the assembly of individual nanometre-sized particles into arrays of micrometre-sized aggregates, whose size and characteristic spacing can be tuned by varying the cooling rate. This fully reversible process offers hierarchical control over structural order on the molecular, nanoscopic, and microscopic level and is an interesting model system for the programmable patterning of nanocomposites with access to micrometre-sized periodicities.

Annealing effect on the optical and photoelectrochemical properties of lead oxide

2018 ◽  
Vol 84 (3) ◽  
pp. 30301 ◽  
Author(s):  
Wided Zerguine ◽  
Djamila Abdi ◽  
Farid Habelhames ◽  
Meriem Lakhdari ◽  
Hassina Derbal-Habak ◽  
...  
Keyword(s):  
Lead Oxide ◽  
Orthorhombic Phase ◽  
Heat Treatments ◽  
Photoelectrochemical Properties ◽  
X Ray Diffraction ◽  
Vis Spectroscopy ◽  
Size And Morphology ◽  
Two Phases ◽  
P Type ◽  
The Relationship

Effect of the annealing oxidation time of electrodeposited lead (Pb) on the phase formation of lead oxide (PbO) films is reported. The phase structure, optical properties, size and morphology of the films were investigated by scanning electron microscopy, X-ray diffraction and UV-vis spectroscopy. The relationship between structur and photoelectrochemical properties was investigated. Thin films of PbO produced via air annealing of electrodeposited lead consist of a mixture of two phases, orthorhombic (o-PbO) and tetragonal (t-PbO), that determine the material properties and effectiveness as absorber layer in a photoelectrochemical device. The proportion of tetragonal t-PbO increases for longer heat treatments. After 40 h, the sample consists mainly of tetragonal t-PbO. The p-type semiconducting behavior of lead oxide was studied by photocurrent measurements. Different heat treatments yield variations in the ratio of tetragonal to orthorhombic lead oxide that effect on device performances, where devices with a higher content of tetragonal t-PbO show higher photocurrent than with the orthorhombic phase.

Fe@B6H6 Aggregates: From Simple Building Blocks to Graphene Analogue

2021 ◽  
Author(s):  
Chao Wang ◽  
Jianhua Hou ◽  
Qian Duan
Keyword(s):  
Building Block ◽  
Building Blocks ◽  
Electron Structure ◽  
Chemical Doping ◽  
Hole Density ◽  
Hexagonal Hole

Abstract We suggest the possibility to build graphene analogue with the planar hexacoordinate wheel-type Fe@B6H6 cluster as the building block through studying theoretically the geometry, stability and electron structure of its dimer and trimer as well as the dimerization of the two trimers. Employing the dehydrogenation route to polymerization, we can obtain the hexagonal boron sheet that are partly and uniformly filled by Fe atoms in the center of the holes, achieving uniform chemical doping and a very large hexagonal-hole-density. Thus, we may offer a novel cluster-assembled material for experimental chemists to construct graphene analogue.

scholarly journals Synthesis of new Cα-tetrasubstituted α-amino acids

2009 ◽  
Vol 5 ◽  
Author(s):  
Andreas A Grauer ◽  
Burkhard König
Keyword(s):  
Amino Acids ◽  
Secondary Structure ◽  
Aromatic Aldehydes ◽  
Building Blocks ◽  
Reaction Conditions ◽  
Peptide Backbone ◽  
Aliphatic Aldehydes ◽  
New Class ◽  
Cyclic Amino Acids

Cα-Tetrasubstituted α-amino acids are important building blocks for the synthesis of peptidemimetics with stabilized secondary structure, because of their ability to rigidify the peptide backbone. Recently our group reported a new class of cyclic Cα-tetrasubstituted tetrahydrofuran α-amino acids prepared from methionine and aromatic aldehydes. We now report the extension of this methodology to aliphatic aldehydes. Although such aldehydes are prone to give aldol products under the reaction conditions used, we were able to obtain the target cyclic amino acids in low to moderate yields and in some cases with good diastereoselectivity.

Syntheses and Properties of k-Phase Organic Superconductors

1992 ◽  
Vol 247 ◽  
Author(s):  
H. Hau Wang ◽  
K. D. Carlson ◽  
U. Geiser ◽  
A. M. Kini ◽  
A. J. Schultz ◽  
...  
Keyword(s):  
Phase Transition ◽  
Ambient Pressure ◽  
Density Wave ◽  
Spin Density Wave ◽  
Organic Superconductors ◽  
Organic Superconductor ◽  
X Ray ◽  
New Class ◽  
Structural Differences ◽  
Similarities And Differences

ABSTRACTThe syntheses and physical properties of K-(ET)2CU[N(CN)2]X (X = Br and Cl) are summarized. The K-(ET)2Cu [N(CN)2] Br salt is the highest Tc radical-cation based ambient pressure organic superconductor (Tc = 11.6 K), and the K-(ET)2CU [N(CN)2] C1 salt becomes a superconductor at even higher Tc under 0.3 kbar hydrostatic pressure (Tc = 12.8 K). The similarities and differences between K-(ET)2Cu[N(CN)2]Br and K-(ET)2CU(NCS)2 (TC = 10.4 K) are presented. The X-ray structures at 127 K reveal that the S-S contacts shorten between ET dimers in the former compound while the S-S contacts shorten within dimers in the latter. The differences in their ESR linewidth behavior is also explained in terms of the structural differences. A semiconducting compound, (ET)Cu[N(CN)2]2, isolated during K-(ET)2Cu[N(CN)2]Cl synthesis is also reported. The ESR measurements of the K-(ET)2Cu[N(CN)2]Cl salt indicate that the phase transition near 40 K is similar to the spin density wave transition in (TMTSF)2SbF6. A new class of organic superconductors, K-(ET)2CU2(CN)3 and K-(ET)2Cu2(CN)3.δBrδ, is reported with Tc's of 2.8 K (1.5 kbar) and 2.6 K (1 kbar), respectively.

Temperature Driven Phase Transition of Organic-Inorganic Halide Perovskite Single Crystals

2018 ◽  
Vol 73 (11) ◽  
pp. 1729-1734
Author(s):  
Hye Ryung Byun ◽  
Hyo In Kim ◽  
Su Jeong Byun ◽  
Dae Young Park ◽  
Mun Seok Jeong ◽  
...  
Keyword(s):  
Phase Transition ◽  
Single Crystals ◽  
Halide Perovskite

scholarly journals Cu/Pd-catalyzed borocarbonylative trifunctionalization of alkynes and allenes: synthesis of β-geminal-diboryl ketones

2021 ◽  
Author(s):  
Yang Yuan ◽  
Fu-Peng Wu ◽  
Anke Spannenberg ◽  
Xiao-Feng Wu
Keyword(s):  
Organic Synthesis ◽  
Functional Group ◽  
Building Blocks ◽  
Mechanistic Studies ◽  
Efficient Strategy ◽  
New Class ◽  
Reaction Proceeds

AbstractFunctionalized bisboryl compounds have recently emerged as a new class of synthetically useful building blocks in organic synthesis. Herein, we report an efficient strategy to synthesize β-geminal-diboryl ketones enabled by a Cu/Pd-catalyzed borocarbonylative trifunctionalization of readily available alkynes and allenes. This reaction promises to be a useful method for the synthesis of functionalized β-geminal-diboryl ketones with broad functional group tolerance. Mechanistic studies suggest that the reaction proceeds through borocarbonylation/hydroboration cascade of both alkynes and allenes.

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