Phosphide — chemistry, structure, reactions and applications
Phosphide describes compounds containing phosphorus in a low (often −3) oxidation state, from the discrete P3− ion to covalent/metallic phosphides. Covers bonding, reactions (phosphine), examples and uses.
Overview
In chemistry, "phosphide" refers to materials that contain phosphorus in a reduced form. In simple ionic salts the phosphorus exists formally as the phosphide anion, commonly written as P3−, and behaves as a strong reducing species. However, many compounds called phosphides are covalent or metallic intermetallic phases rather than salts with discrete P3− ions.
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Ionic phosphides, found with highly electropositive metals, contain isolated P3− centers and are described as salts. An example often cited is sodium phosphide. By contrast, binary phosphides of transition and post-transition metals display a range of bonding: some are covalent semiconductors such as gallium phosphide and indium phosphide, while others are metallic intermetallics or form networks and clusters (polyphosphides). The formal oxidation state in ionic phosphides is −3, but in covalent or metallic phosphides the electron distribution is more delocalized.
Reactivity and safety
Phosphides are generally reducing and react with acids to release phosphine (PH3), a toxic and flammable gas: for this reason such reactions must be handled with care. The simple description "phosphide → phosphine on acidification" is broadly true for ionic phosphides. Some metal phosphides are much less reactive because their P atoms are embedded in covalent or metallic lattices.
Examples and notable compounds
- Alkali and alkaline earth phosphides — typically ionic and highly reactive toward protic media.
- Metallic phosphides — occur as intermetallic phases and may be corrosion-resistant or catalytic.
- Semiconductor phosphides — compounds such as GaP and InP are important in optoelectronics and high-speed electronics.
- Polyphosphides — species in which phosphorus atoms form chains or clusters with fractional charges.
Preparation and natural occurrence
Phosphides are prepared by direct combination of the elements at elevated temperatures, by high-temperature solid-state reactions, or by reduction of phosphorus compounds. Some phosphides occur naturally: iron‑nickel phosphide minerals are found in meteorites and are studied for insights into planetary chemistry. Industrial and laboratory methods vary with the desired phase and reactivity.
Applications and distinctions
Phosphides are significant in materials science and industry. Semiconductor phosphides are used in LEDs, lasers and photonics, while certain transition metal phosphides have catalytic roles and are investigated for battery and hydrogen-evolution applications. A key distinction for users is whether a phosphide is ionic (containing discrete P3−) or non‑ionic (covalent/metallic): this controls its reactivity, stability, and practical handling. For further reading see general references and specialized reviews at technical sources.
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AlegsaOnline.com Phosphide — chemistry, structure, reactions and applications Leandro Alegsa
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