MnTe2O5

MnTe2O5 is a semiconducting manganese tellurite oxide studied for its potential role as a catalyst in oxygen-evolution reactions.

Crystal structure of MnTe2O5 (orthorhombic, Pbcn (No. 60))
Ground-state structure · Materials Project
Overview

About MnTe2O5

MnTe2O5 is a semiconducting oxide that sits near the thermodynamic hull, indicating it is a promising candidate for experimental synthesis. Its unique arrangement of manganese and tellurium polyhedra makes it a compelling subject for researchers investigating new materials for electrocatalytic water splitting.

As an emerging member of the oxide oxygen-evolution catalyst class, this compound is being evaluated for its potential to facilitate electrochemical reactions. Its electronic structure and structural stability provide a foundation for exploring efficient, earth-abundant alternatives to precious metal-based catalysts in energy storage and conversion systems.

At a glance

Key Properties

Cross-validated computational properties for MnTe2O5, aggregated across 4 databases.

Band Gap

1.72–2.13 eV
Range across DFT structures

Energy Above Hull

0.010 eV/atom
Best (lowest) across sources

Stability

Near hull (likely stable)
2 DFT sources

Structures

8
4 databases, 4 space groups
Crystallography

Reported Structures

Lowest-energy structures reported for MnTe2O5, ranked by energy above hull.

Space GroupCrystal SystemBand Gap (eV)E above hull (eV/atom)E/atom (eV)Density (g/cm³)
Pbcn (No. 60)orthorhombic1.720.0095-6.7045.31
P42/nbc (No. 133)tetragonal2.130.0124-6.7014.93
P21212 (No. 18)orthorhombic2.070.0166-6.6975.18
P21212 (No. 18)Orthorhombic5.18
Pbcn (No. 60)Orthorhombic5.45
Pbcn (No. 60)Orthorhombic5.27
Pbcn (No. 60)
No. 0unknown0.37
Uses

Applications

Where MnTe2O5 is used.

Oxygen-evolution catalysisElectrochemical energy conversionMaterials science research
Reference

Frequently Asked Questions

Common questions about MnTe2O5, answered from cross-validated data.

What is MnTe2O5?

MnTe2O5 is a semiconducting manganese tellurite oxide studied for its potential role as a catalyst in oxygen-evolution reactions.

More questions
What is MnTe2O5 used for?
MnTe2O5 is used in oxygen-evolution catalysis, electrochemical energy conversion, and materials science research.
What is the band gap of MnTe2O5?
MnTe2O5 has a DFT-computed band gap of 1.72–2.13 eV across 8 reported structures.
Is MnTe2O5 a metal, semiconductor, or insulator?
With a band gap up to 2.13 eV it is a semiconductor.
Is MnTe2O5 thermodynamically stable?
MnTe2O5 has a lowest energy above hull of 0.010 eV/atom (near hull (likely stable)).
What is the crystal structure of MnTe2O5?
The lowest-energy reported polymorph of MnTe2O5 is orthorhombic symmetry, space group Pbcn (No. 60).
What is the density of MnTe2O5?
The computed density of the ground-state structure of MnTe2O5 is 5.31 g/cm³.
How many polymorphs of MnTe2O5 are known?
8 structures of MnTe2O5 are reported across 4 databases, spanning 4 distinct space groups.
What elements does MnTe2O5 contain?
MnTe2O5 contains Mn, O, and Te (3 elements).
Where does the data for MnTe2O5 come from?
MnTe2O5 data is cross-referenced from materials_project, mpaloe, jarvis, cod.
Comparison

How It Compares

Within the oxide oxygen-evolution catalysts class.

Unlike the well-established battery cathode materials such as LiCoO2 or LiMn2O4, MnTe2O5 represents a more specialized, exploratory approach to catalysis. While perovskites like LaMnO3 are widely recognized for their catalytic activity, MnTe2O5 offers a distinct chemical environment that may provide unique advantages in specific oxygen-evolution reaction pathways compared to traditional transition metal oxides.

Explore

Related Compounds

Other Oxide Oxygen-Evolution Catalysts in the database.

Data sources & attribution
  • materials_project — Data from the Materials Project. Cite: Jain et al., APL Materials 1, 011002 (2013).
  • mpaloe — Data from mpaloe.
  • jarvis — Data from JARVIS (NIST). Cite: Choudhary et al., npj Comp. Mater. 6, 173 (2020).
  • cod — Data from the Crystallography Open Database. Cite: Grazulis et al., Nucleic Acids Res. 40, D420 (2012).

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