121239-75-6 Purity
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Specification
A photocatalyst with high visible light capture efficiency was successfully designed and prepared by anchoring lithium manganate nanoparticles (Li2MnO3 NPs) on a mesoporous ceria (CeO2) network. The obtained Li2MnO3/CeO2 nanocomposite can be used for photoreduction of Hg(II) ions under visible light irradiation and exhibits high stability and high efficiency.
Key properties of Li2MnO3/CeO2 nanocomposite
· The presence of Li2MnO3 and CeO2 in the nanocomposites, exhibiting monoclinic and cubic fluorite structures with particle sizes ranging from 10 to 20 nm.
· Compared to pristine CeO2 nanoparticles, the incorporation of Li2MnO3 and CeO2 NPs resulted in remarkable enhancement of photocatalytic activity. The optimal 9% Li2MnO3/CeO2 composite exhibited a remarkable 98% reduction ability for Hg(II) within 60 minutes. The rate constant of the 9% Li2MnO3/CeO2 photocatalyst was approximately 6.47 and 3.85 times higher than that of Li2MnO3 and CeO2 NPs, respectively.
· This superior performance can be attributed to the efficient separation of photocarriers facilitated by the S-scheme heterojunction, large surface area, and mesoporous structures of the Li2MnO3/CeO2 nanocomposites.
· Furthermore, the stability and efficiency of the Li2MnO3/CeO2 nanocomposites were demonstrated by consistent Hg(II) photoreduction performance over five successive experiments under similar conditions.
Layered spinel lithium manganate hydrate (LHMO-LS) was successfully synthesized via a one-step hydrothermal lithiation process, which has a hierarchical structure consisting of two-dimensional nanosheets. Subsequently, the electrochemical performance of LHMO-LS as a cathode material for lithium-ion batteries was studied. The results show that the LHMO-LS material combines diffusion-controlled and pseudocapacitive charge storage mechanisms, with high capacity output and high rate capability.
Synthesis procedure of LHMO-LS material
· The synthesis of lithium manganite hydrates with layered-spinel phases (referred to as LHMO-LS) was carried out using a straightforward hydrothermal method. Initially, 5 mmol of birnessite-type manganese oxides were combined with 60 mL of 0.06 M LiOH aqueous solution, and then transferred into a 100 mL Teflon-lined stainless steel autoclave.
· Subsequently, the hydrothermal reaction took place for 48 hours at 160°C in an oven. Finally, the resulting precipitate was filtered under vacuum, washed, and dried at 70°C for 10 hours.
· Additionally, by adjusting the concentration of the LiOH solution, control samples of lithium manganese oxide with a single hydrated layered phase (referred to as LHMO-L) containing 0.04 M LiOH and lithium manganese oxide with a single unhydrous spinel phase (LMO-S) containing 0.16 M LiOH were easily prepared.
The molecular formula of lithium manganite is Li2MnO3.
Some synonyms for lithium manganite are lithium manganate(IV) and lithium dioxido(oxo)manganese.
The molecular weight of lithium manganite is 116.9 g/mol.
The IUPAC name of lithium manganite is dilithium;dioxido(oxo)manganese.
The InChI of lithium manganite is InChI=1S/2Li.Mn.3O/q2*+1;;;2*-1.
The InChIKey of lithium manganite is MYKKJHPKWUYDHJ-UHFFFAOYSA-N.
The canonical SMILES of lithium manganite is [Li+].[Li+].[O-][Mn](=O)[O-].
Lithium manganite has 3 hydrogen bond acceptor counts.
The topological polar surface area of lithium manganite is 63.2Ų.
Yes, lithium manganite is a canonicalized compound.