Browse
Submit Data
Databases
API
Help

Dataset Information

30 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Ultrathin palladium nanosheets with selectively controlled surface facets.

ABSTRACT: We report a facile bottom-up synthetic approach to preparing ultrathin two-dimensional (2D) palladium nanosheets (PdNSs) with selectively exposed surface facets. Our synthetic strategy is based on the utilization of the nanoconfined lamellar mesophases of amphiphilic functional surfactants to template the growth of PdNSs in aqueous solution. Preferential adsorption of functional groups (e.g., COOH, pyridyl and quaternary ammonium) and halide counter ions (e.g., Br- and Cl-) in the long-chain surfactants onto different Pd planes results in the epitaxial growth of {100}, {110} and {111}-exposed surface facets of ultrathin PdNSs. Our synthetic approach is a general, powerful and scalable method to precisely control the surface facets of ultrathin 2D PdNSs, thus providing an opportunity to evaluate facet-dependent catalytic performance of Pd nanocrystals. Ultrathin PdNSs have been examined as the electrocatalysts for hydrogen evolution reactions (HERs). We show that {100}-exposed PdNSs display superior catalytic activity and stability for HERs, compared to that of {110} and {111}-exposed ones as well as their bulk counterparts. Conceivably, our findings will offer a general guideline in rational design of surfactant templates for other 2D metal nanosheets.

SUBMITTER: Xu D

PROVIDER: S-EPMC5956979 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Functionalized ultrathin palladium nanosheets as patches for HepG2 cancer cells.

Project description:Flexible, charged Pd nanosheets were prepared by using short chain thiolated carboxylic acids and amines. They could wrap around amine or hydroxyl functionalized micron-sized spheres driven by electrostatic interactions. Upon incubation with HepG2 cells, the positively charged cysteamine (CA) functionalized Pd nanosheets exhibited a much higher cytotoxicity, showing more than 80% cell death at 100 ppm than the negatively charged 3-mercaptopropionic acid (MPA) functionalized ones which caused 30% cell death. The results show through surface functionalization Pd nanosheets can be modified to interact differently with HepG2 cancerous cells, resulting in varied cytotoxicity.

| S-EPMC4560650 | biostudies-literature

Cancer-derived exosomes loaded with ultrathin palladium nanosheets for targeted bioorthogonal catalysis.

Project description:The transformational impact of bioorthogonal chemistries has inspired new strategies for the in vivo synthesis of bioactive agents through non-natural means. Among these, palladium (Pd) catalysts have played a prominent role in the growing subfield of bioorthogonal catalysis by producing xenobiotics and uncaging biomolecules in living systems. However, delivering catalysts selectively to specific cell types still lags behind catalyst development. Here we have developed a bio-artificial device consisting of cancer-derived exosomes loaded with Pd catalysts by a method that enables the controlled assembly of Pd nanosheets directly inside the vesicles. This hybrid system mediates Pd-triggered dealkylation reactions in vitro and inside cells and displays preferential tropism for their progenitor cells. The use of Trojan exosomes to deliver abiotic catalysts into designated cancer cells creates the opportunity for a new targeted therapy modality: exosome-directed catalyst prodrug therapy, whose first steps are presented herein with the cell-specific release of the anticancer drug panobinostat.

| S-EPMC6795537 | biostudies-literature

Thickness-controlled electronic structure and thermoelectric performance of ultrathin SnS2 nanosheets.

Project description:The thermoelectric conversion efficiency of a material relies on a dimensionless parameter (ZT = S 2 σT/κ). It is a great challenge in enhancing the ZT value basically due to that the related transport factors of most of the bulk materials are inter-conditioned to each other, making it very difficult to simultaneously optimize these parameters. In this report, the negative correlation between power factor and thermal conductivity of nano-scaled SnS2 multilayers is predicted by high-level first-principle computations combined with Boltzmann transport theory. By diminishing the thickness of SnS2 nanosheet to about 3 L, the S and σ along a direction simultaneously increase whereas κ decreases, achieving a high ZT value of 1.87 at 800 K. The microscopic mechanisms for this unusual negative correlation in nano-scaled two dimensional (2D) material are elucidated and attributed to the quantum confinement effect. The results may open a way to explore the high ZT thermoelectric nano-devices for the practical thermoelectric applications.

| S-EPMC5567102 | biostudies-literature

A Chelation Strategy for In-situ Constructing Surface Oxygen Vacancy on {001} Facets Exposed BiOBr Nanosheets.

Project description:Surface defect of nanomaterials is an important physical parameter which significantly influences their physical and chemical performances. In this work, high concentration of surface oxygen vancancies (SOVs) are successfully introduced on {001} facets exposed BiOBr nanosheets via a simple surface modification using polybasic carboxylic acids. The chelation interaction between carboxylic acid anions and Bi(3+) results in the weakness of Bi-O bond of BiOBr. Afterwards, under visible-light irradiation, the oxygen atoms would absorb the photo-energy and then be released from the surface of BiOBr, leaving SOVs. The electron spin resonance (ESR), high-resolution transmission electron microscopy (HRTEM), and UV-vis diffuse reflectance spectra (DRS) measurements confirm the existence of SOVs. The SOVs can enhance the absorption in visible light region and improve the separation efficiency of photo-generated charges. Hence, the transformation rate of adsorbed O2 on the as-prepared BiOBr with SOVs to superoxide anion radicals (•O2(-)) and the photocatalytic activity are greatly enhanced. Based on the modification by several carboxylic acids and the photocatalytic results, we propose that carboxylic acids with natural bond orbital (NBO) electrostatic charges absolute values greater than 0.830 are effective in modifying BiOBr.

| S-EPMC4845065 | biostudies-literature

Sub-1.1 nm ultrathin porous CoP nanosheets with dominant reactive {200} facets: a high mass activity and efficient electrocatalyst for the hydrogen evolution reaction.

Project description:The exploration of a facile strategy to synthesize porous ultrathin nanosheets of non-layered materials, especially with exposed reactive facets, as highly efficient electrocatalysts for the hydrogen evolution reaction (HER), remains challenging. Herein we demonstrate a chemical transformation strategy to synthesize porous CoP ultrathin nanosheets with sub-1.1 nm thickness and exposed {200} facets via phosphidation of Co3O4 precursors. The resultant samples exhibit outstanding electrochemical HER performance: a low overpotential (only 56 and 131 mV are required for current densities of 10 and 100 mA cm-2, respectively), a small Tafel slope of 44 mV per decade, a good stability of over 20 h, and a high mass activity of 151 A g-1 at an overpotential of 100 mV. The latter is about 80 times higher than that of CoP nanoparticles. Experimental data and density functional theory calculations reveal that a high proportion of reactive {200} facets, high utilization efficiency of active sites, metallic nature, appropriate structural disorder, facile electron/mass transfer and rich active sites benefiting from the unique ultrathin and porous structure are the key factors for the greatly improved activity. Additionally, this facile chemical conversion strategy can be developed to a generalized method for preparing porous ultrathin nanosheets of CoSe2 and CoS that cannot be obtained using other methods.

| S-EPMC5426437 | biostudies-literature

Controlled growth of NiCo?O? nanorods and ultrathin nanosheets on carbon nanofibers for high-performance supercapacitors.

Project description:Two one-dimensional hierarchical hybrid nanostructures composed of NiCo2O4 nanorods and ultrathin nanosheets on carbon nanofibers (CNFs) are controllably synthesized through facile solution methods combined with a simple thermal treatment. The structure of NiCo2O4 can be easily controlled to be nanorods or nanosheets by using different additives in the synthesis. These two different nanostructures are evaluated as electrodes for high performance supercapacitors, in view of their apparent advantages, such as high electroactive surface area, ultrathin and porous features, robust mechanical strength, shorter ion and electron transport path. Their electrochemical performance is systematically studied, and both of these two hierarchical hybrid nanostructures exhibit high capacitance and excellent cycling stability. The remarkable electrochemical performance will undoubtedly make these hybrid structures attractive for high-performance supercapacitors with high power and energy densities.

| S-EPMC3600593 | biostudies-literature

Controlled Synthesis of Ultrathin PtSe<sub>2</sub> Nanosheets with Thickness-Tunable Electrical and Magnetoelectrical Properties.

Project description:Thickness-dependent chemical and physical properties have gained tremendous interest since the emergence of two-dimensional (2D) materials. Despite attractive prospects, the thickness-controlled synthesis of ultrathin nanosheets remains an outstanding challenge. Here, a chemical vapor deposition (CVD) route is reported to controllably synthesize high-quality PtSe2 nanosheets with tunable thickness and explore their thickness-dependent electronic and magnetotransport properties. Raman spectroscopic studies demonstrate all Eg , A1 g , A2 u , and Eu modes are red shift in thicker nanosheets. Electrical measurements demonstrate the 1.7 nm thick nanosheet is a semiconductor with room temperature field-effect mobility of 66 cm2 V-1 s-1 and on/off ratio of 106 . The 2.3-3.8 nm thick nanosheets show slightly gated modulation with high field-effect mobility up to 324 cm2 V-1 s-1 at room-temperature. When the thickness is over 3.8 nm, the nanosheets show metallic behavior with conductivity and breakdown current density up to 6.8 × 105 S m-1 and 6.9 × 107 A cm-2 , respectively. Interestingly, magnetoresistance (MR) studies reveal magnetic orders exist in this intrinsically non-magnetic material system, as manifested by the thickness-dependent Kondo effect, where both metal to insulator transition and negative MR appear upon cooling. Together, these studies suggest that PtSe2 is an intriguing system for both developing novel functional electronics and conducting fundamental 2D magnetism study.

| S-EPMC8728827 | biostudies-literature

Screen-Printable Electronic Ink of Ultrathin Boron Nitride Nanosheets.

Project description:Two-dimensional materials play a vital role in the current electronic industry in the fabrication of devices. In the present work, we have exfoliated and stabilized the insulating hexagonal boron nitride (hBN) by means of a polymer-assisted liquid-phase technique. Further, the highly viscous ink of hBN was prepared, and its printability on various commercially available substrates was studied. The morphology of the printed patterns reveals the layered arrangement of hBN. The various electrical and dielectric characterizations, carried out on a metal-insulator-metal capacitor, testified its potential applications in various fields of printed electronics.

| S-EPMC6640765 | biostudies-literature

Excellent humidity sensor based on ultrathin HKUST-1 nanosheets.

Project description:The copper-based MOF, HKUST-1 has been applied for humidity sensing owing to hydrophilic ligands and open metal sites which are suitable for sensitively detecting moisture. However, most of the research on the sensor HKUST-1 focuses on the role of the central metal. There are few reports on the morphology-activity relationship of HKUST-1. In this work, we synthesized two kinds of HKUST-1 including octahedral structures and ultrathin nanosheets, and systematically studied the performance of moisture sensing. Compared to HKUST-1 octahedra, HKUST-1 nanosheets showed lower and wider detectable humidity range, achieving a fast response. Starting from the exposed hydrophilic functional groups of HKUST-1 nanosheets, we have revealed that hydrophilic ligands play an important role in improving the adsorption capacity during the adsorption process. In addition, ultra-thin HKUST-1 nanosheets act as an excellent mass transfer medium, accelerating proton transfer and water molecule movement. To further improve the performance of the HKUST-1 humidity sensor, black phosphorus quantum dots (BPQDs) with a high surface reactivity were used to build a composite sensing platform. The excellent proton transfer capability of BPQDs leads to one order of magnitude improvement in the sensitivity of the BPQDs/HKUST-1 systems compared to HKUST-1 only.

| S-EPMC8690182 | biostudies-literature

Gas-phase microactuation using kinetically controlled surface states of ultrathin catalytic sheets.

Project description:Biological systems convert chemical energy into mechanical work by using protein catalysts that assume kinetically controlled conformational states. Synthetic chemomechanical systems using chemical catalysis have been reported, but they are slow, require high temperatures to operate, or indirectly perform work by harnessing reaction products in liquids (e.g., heat or protons). Here, we introduce a bioinspired chemical strategy for gas-phase chemomechanical transduction that sequences the elementary steps of catalytic reactions on ultrathin (<10 nm) platinum sheets to generate surface stresses that directly drive microactuation (bending radii of 700 nm) at ambient conditions (T = 20 °C; Ptotal = 1 atm). When fueled by hydrogen gas and either oxygen or ozone gas, we show how kinetically controlled surface states of the catalyst can be exploited to achieve fast actuation (600 ms/cycle) at 20 °C. We also show that the approach can integrate photochemically controlled reactions and can be used to drive the reconfiguration of microhinges and complex origami- and kirigami-based microstructures.

| S-EPMC10175785 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data