Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Amino-Functionalized Titanium Based Metal-Organic Framework for Photocatalytic Hydrogen Production.

ABSTRACT: Photocatalytic hydrogen production using stable metal-organic frameworks (MOFs), especially the titanium-based MOFs (Ti-MOFs) as photocatalysts is one of the most promising solutions to solve the energy crisis. However, due to the high reactivity and harsh synthetic conditions, only a limited number of Ti-MOFs have been reported so far. Herein, we synthesized a new amino-functionalized Ti-MOFs, named NH₂-ZSTU-2 (ZSTU stands for Zhejiang Sci-Tech University), for photocatalytic hydrogen production under visible light irradiation. The NH₂-ZSTU-2 was synthesized by a facile solvothermal method, composed of 2,4,6-tri(4-carboxyphenylphenyl)-aniline (NH₂-BTB) triangular linker and infinite Ti-oxo chains. The structure and photoelectrochemical properties of NH₂-ZSTU-2 were fully studied by powder X-ray diffraction, scanning electron microscope, nitro sorption isotherms, solid-state diffuse reflectance absorption spectra, and Mott-Schottky measurements, etc., which conclude that NH₂-ZSTU-2 was favorable for photocatalytic hydrogen production. Benefitting from those structural features, NH₂-ZSTU-2 showed steady hydrogen production rate under visible light irradiation with average photocatalytic H₂ yields of 431.45 μmol·g^-1·h^-1 with triethanolamine and Pt as sacrificial agent and cocatalyst, respectively, which is almost 2.5 times higher than that of its counterpart ZSTU-2. The stability and proposed photocatalysis mechanism were also discussed. This work paves the way to design Ti-MOFs for photocatalysis.

SUBMITTER: Hu N

PROVIDER: S-EPMC9268624 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Enhanced photocatalytic performance of a Ti-based metal-organic framework for hydrogen production: Hybridization with ZnCr-LDH nanosheets.

Project description:Novel hybrid composites of NH2-MIL-125(Ti) and ZnCr-layered double hydroxide nanosheets (ZnCr-LDH NSs) are developed for use as visible-light-active photocatalysts for hydrogen production based on water photolysis. The hybrid composites are obtained by growing NH2-MIL-125(Ti) in the presence of exfoliated ZnCr-LDH NSs using a solvothermal reaction. Hybridization of NH2-MIL-125(Ti) with exfoliated ZnCr-LDH NSs leads to significant effects on the morphology and optical properties of NH2-MIL-125(Ti). To find the optimum photocatalytic activity for hydrogen production by the hybrid composite photocatalysts, the content of ZnCr-LDH in this work is controlled. Compared to that of pristine NH2-MIL-125(Ti) and ZnCr-LDH, the hybrid composites exhibit an improved photocatalytic activity for hydrogen production under visible-light irradiation. In addition, the hybrid composite photocatalyst shows excellent photo-chemical stability. The improved photocatalytic activity is believed to benefit from the synergy of strong electronic coupling between NH2-MIL-125(Ti) and ZnCr-LDH NSs, expanded light absorption and band alignment to enhance the lifetime of photo-induced electrons and holes.

| S-EPMC6527569 | biostudies-literature

Metal-Organic Framework-Derived ZnO/ZnS Heteronanostructures for Efficient Visible-Light-Driven Photocatalytic Hydrogen Production.

Project description:Developing highly active, recyclable, and inexpensive photocatalysts for hydrogen evolution reaction (HER) under visible light is significant for the direct conversion of solar energy into chemical fuels for various green energy applications. For such applications, it is very challenging but vitally important for a photocatalyst to simultaneously enhance the visible-light absorption and suppress photogenerated electron-hole recombination, while also to maintain high stability and recyclability. Herein, a metal-organic framework (MOF)-templated strategy has been developed to prepare heterostructured nanocatalysts with superior photocatalytic HER activity. Very uniquely, the synthesized photocatalytic materials can be recycled easily after use to restore the initial photocatalytic activity. It is shown that by controlling the calcination temperature and time with MOF-5 as a host and guest thioacetamide as a sulfur source, the chemical compositions of the formed heterojunctions of ZnO/ZnS can be tuned to further enhance the visible-light absorption and photocatalytic activity. The nanoscale heterojunction ZnO/ZnS structural feature serves to reduce the average free path of charge carriers and improve the charge separation efficiency, thus leading to significantly enhanced HER activity under visible-light irradiation (? > 420 nm) with high stability and recyclability without any cocatalyst.

| S-EPMC5908348 | biostudies-literature

Facet-dependent photocatalytic hydrogen production of metal-organic framework NH<sub>2</sub>-MIL-125(Ti).

Project description:Facet-dependent catalytic activity of hard materials such as metals and metal oxides is well recognized in previous works. However, it has rarely been established for metal-organic frameworks (MOFs), possibly because the soft crystals of MOFs are conceptually different from the hard solids. In this work, the surface structure of the MOF NH2-MIL-125(Ti) has been investigated by density functional theory (DFT) calculations for the first time. These calculations predict that the {110} facet has a surface energy of 1.18 J m-2, which is superior to those of the {001}, {100} and {111} facets. This difference can be attributed to the larger percentage of exposed metal clusters, which can act as active sites in catalysis. Thus, we have devised and successfully obtained a series of nanoscaled NH2-MIL-125(Ti) MOFs with controlled facets both experimentally and theoretically. The sample containing the {110} facet exhibits the highest photocatalytic hydrogen production activity and apparent quantum yield, which are approximately three times those of the sample with a dominant {111} facet.

| S-EPMC6509995 | biostudies-literature

A malonitrile-functionalized metal-organic framework for hydrogen sulfide detection and selective amino acid molecular recognition.

Project description:A novel porous polymeric fluorescence probe, MN-ZIF-90, has been designed and synthesized for quantitative hydrogen sulfide (H2S) fluorescent detection and highly selective amino acid recognition. This distinct crystalline structure, derived from rational design and malonitrile functionalization, can trigger significant enhancement of its fluorescent intensity when exposed to H2S or cysteine molecules. Indeed this new metal-organic framework (MOF) structure shows high selectivity of biothiols over other amino acids and exhibits favorable stability. Moreover, in vitro viability assays on HeLa cells show low cytotoxicity of MN-ZIF-90 and its imaging contrast efficiency is further demonstrated by fluorescence microscopy studies. This facile yet powerful strategy also offers great potential of using open-framework materials (i.e. MOFs) as the novel platform for sensing and other biological applications.

| S-EPMC3952146 | biostudies-literature

Label-free Electrochemical Detection of ATP Based on Amino-functionalized Metal-organic Framework.

Project description:A sensitive, selective and recyclable electrochemical sensor is designed for ATP detection based on amino-functionalized metal-organic framework. The functional MOF as the sensor is constructed by one-step synthesis Ce-MOF and sequentially modified on the Au electrode and conjugated with the aptamer of ATP. The presence of target ATP leads to the conformational change of aptamer strands and strong electrochemical impedance. The electrochemical sensor can detect ATP down to 5.6?nM with the linear range of 10?nm to 1000??M. The present study is the first report on the use of MOF as an electrochemical sensor for ATP at nM level. This strategy has been successfully applied in detection of ATP in serum of cancer patients, which reveals its potential application in clinical diagnosis.

| S-EPMC5529508 | biostudies-literature

A single crystalline porphyrinic titanium metal-organic framework.

Project description:We successfully assembled the photocatalytic titanium-oxo cluster and photosensitizing porphyrinic linker into a metal-organic framework (MOF), namely PCN-22. A preformed titanium-oxo carboxylate cluster is adopted as the starting material to judiciously control the MOF growth process to afford single crystals. This synthetic method is useful to obtain highly crystalline titanium MOFs, which has been a daunting challenge in this field. Moreover, PCN-22 demonstrated permanent porosity and photocatalytic activities toward alcohol oxidation.

| S-EPMC5707486 | biostudies-other

Toward Optimal Photocatalytic Hydrogen Generation from Water Using Pyrene-Based Metal-Organic Frameworks.

Project description:Metal-organic frameworks (MOFs) are promising materials for the photocatalytic H2 evolution reaction (HER) from water. To find the optimal MOF for a photocatalytic HER, one has to consider many different factors. For example, studies have emphasized the importance of light absorption capability, optical band gap, and band alignment. However, most of these studies have been carried out on very different materials. In this work, we present a combined experimental and computation study of the photocatalytic HER performance of a set of isostructural pyrene-based MOFs (M-TBAPy, where M = Sc, Al, Ti, and In). We systematically studied the effects of changing the metal in the node on the different factors that contribute to the HER rate (e.g., optical properties, the band structure, and water adsorption). In addition, for Sc-TBAPy, we also studied the effect of changes in the crystal morphology on the photocatalytic HER rate. We used this understanding to improve the photocatalytic HER efficiency of Sc-TBAPy, to exceed the one reported for Ti-TBAPy, in the presence of a co-catalyst.

| S-EPMC8662633 | biostudies-literature

Electrocatalytic Hydrogen Evolution from a Cobaloxime-Based Metal-Organic Framework Thin Film.

Project description:Molecular hydrogen evolution catalysts (HECs) are synthetically tunable and often exhibit high activity, but they are also hampered by stability concerns and practical limitations associated with their use in the homogeneous phase. Their incorporation as integral linker units in metal-organic frameworks (MOFs) can remedy these shortcomings. Moreover, the extended three-dimensional structure of MOFs gives rise to high catalyst loadings per geometric surface area. Herein, we report a new MOF that exclusively consists of cobaloximes, a widely studied HEC, that act as metallo-linkers between hexanuclear zirconium clusters. When grown on conducting substrates and under applied reductive potential, the cobaloxime linkers promote electron transport through the film as well as function as molecular HECs. The obtained turnover numbers are orders of magnitude higher than those of any other comparable cobaloxime system, and the molecular integrity of the cobaloxime catalysts is maintained for at least 18 h of electrocatalysis. Being one of the very few hydrogen evolving electrocatalytic MOFs based on a redox-active metallo-linker, this work explores uncharted terrain for greater catalyst diversity and charge transport pathways.

| S-EPMC6803166 | biostudies-literature

Enhanced photochemical hydrogen production by a molecular diiron catalyst incorporated into a metal-organic framework.

Project description:A molecular proton reduction catalyst [FeFe](dcbdt)(CO)6 (1, dcbdt = 1,4-dicarboxylbenzene-2,3-dithiolate) with structural similarities to [FeFe]-hydrogenase active sites has been incorporated into a highly robust Zr(IV)-based metal-organic framework (MOF) by postsynthetic exchange (PSE). The PSE protocol is crucial as direct solvothermal synthesis fails to produce the functionalized MOF. The molecular integrity of the organometallic site within the MOF is demonstrated by a variety of techniques, including X-ray absorption spectroscopy. In conjunction with [Ru(bpy)3](2+) as a photosensitizer and ascorbate as an electron donor, MOF-[FeFe](dcbdt)(CO)6 catalyzes photochemical hydrogen evolution in water at pH 5. The immobilized catalyst shows substantially improved initial rates and overall hydrogen production when compared to a reference system of complex 1 in solution. Improved catalytic performance is ascribed to structural stabilization of the complex when incorporated in the MOF as well as the protection of reduced catalysts 1(-) and 1(2-) from undesirable charge recombination with oxidized ascorbate.

| S-EPMC3829681 | biostudies-literature

Photocatalytic Hydrogen Generation from a Visible-Light-Responsive Metal-Organic Framework System: Stability versus Activity of Molybdenum Sulfide Cocatalysts.

Project description:We report the use of two earth abundant molybdenum sulfide-based cocatalysts, Mo3S132- clusters and 1T-MoS2 nanoparticles (NPs), in combination with the visible-light active metal-organic framework (MOF) MIL-125-NH2 for the photocatalytic generation of hydrogen (H2) from water splitting. Upon irradiation (? ? 420 nm), the best-performing mixtures of Mo3S132-/MIL-125-NH2 and 1T-MoS2/MIL-125-NH2 exhibit high catalytic activity, producing H2 with evolution rates of 2094 and 1454 ?mol h-1 gMOF-1 and apparent quantum yields of 11.0 and 5.8% at 450 nm, respectively, which are among the highest values reported to date for visible-light-driven photocatalysis with MOFs. The high performance of Mo3S132- can be attributed to the good contact between these clusters and the MOF and the large number of catalytically active sites, while the high activity of 1T-MoS2 NPs is due to their high electrical conductivity leading to fast electron transfer processes. Recycling experiments revealed that although the Mo3S132-/MIL-125-NH2 slowly loses its activity, the 1T-MoS2/MIL-125-NH2 retains its activity for at least 72 h. This work indicates that earth-abundant compounds can be stable and highly catalytically active for photocatalytic water splitting, and should be considered as promising cocatalysts with new MOFs besides the traditional noble metal NPs.

| S-EPMC6137427 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

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