Ruddlesden-Popper (RP) phases are a type of perovskite structure that consists of two-dimensional perovskite-like slabs interleaved with cations. The general formula of an RP phase is An+1BnX3n+1, where A and B are cations, X is an anion (e.g., oxygen), and n is the number of octahedral layers in the perovskite-like stack. [1] Generally, it has a phase structure that results from the intergrowth of perovskite-type and NaCl-type (i.e., rocksalt-type) structures.
These phases are named after S.N. Ruddlesden and P. Popper, who first synthesized and described a Ruddlesden-Popper structure in 1957. [2] [3]
The general RP formula An+1BnX3n+1 can be written An-1A’2BnX3n+1, where A and A’ are alkali, alkaline earth, or rare earth metals and B is a transition metal. The A cations are located in the perovskite layer and are 12-fold cuboctahedral coordinated by the anions (CN = 12). The A’ cations have a coordination number of 9 (CN = 9) and are located at the boundary between the perovskite layer and an intermediate block layer. The B cations are located inside the anionic octahedra, pyramids and squares. [4]
The first series of Ruddlesden-Popper phases, Sr2TiO4, Ca2MnO4 and SrLaAlO4, were confirmed by powder X-ray diffraction (PXRD) in 1957. [2] These compounds were formed by heating up the appropriate oxides and carbonates in the correct proportions.
In recent years, interest in perovskite-like structures has been growing and methods for synthesizing these compounds have been further developed. In contrast to the conventional solid-state method, chimie douce or soft chemistry techniques are often utilized to synthesize this class of materials. These soft chemistry techniques include ion-exchange reactions of layered perovskites, ion-exchange reactions involving interlayer structural units, topochemical condensation reactions and other techniques such as intercalation-deintercalation reactions and multistep intercalation reactions of layer perovskite. [5]
Similar to the parent perovskite phases, Ruddlesden-Popper phases can possess interesting properties such as colossal magnetoresistance, superconductivity, ferroelectricity, catalytic activity, [6] white light emitting diodes, [7] scintillators, [8] [9] fuel cell, [10] and solar cells. [11] [12]
Using Ruddlesden-Popper perovskite as light-emitting diodes has the advantages of low-cost solution-processing, tunable bandgap, and better stability compared to 3D perovskite. In 2018, Mohite et al. achieved a 14 hours stable operation of 2D (CH3(CH2)3NH3)2(CH3NH3)n-1PbnI3n+1 Ruddlesden-Popper perovskite thin films as light-emitting diodes under operating conditions, while 3D perovskite as light-emitting diodes could degrade within minutes. [13]
The Ruddlesden-Popper phase LaSr3Fe3O10 is an example of a layered perovskite being developed for use in rechargeable metal-air batteries. [14] Due to the layered nature of Ruddlesden-Popper structures, the oxygen located between the perovskite layers is easily removed. The ease of removing the oxygen atoms is responsible for the efficiency of the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in the material. In a metal-air battery, OER is the process of charging that occurs at the air electrode, while ORR is the discharging reaction.
The Ruddlesden-Popper phase perovskites are also prospective candidate materials in energy storage devices. The formula of (R-NH3)2An-1BnX3n+1 are being developed for solar cell. Here, R-NH3+ is long organic chain or cyclic ammonium cation, A is methylamine (MA) or formamidine (FA), B is Pb or Sn, and X is halogen ions. [12] The Ruddlesden-Popper perovskites can also be used for cathode materials of solid oxide fuel cells (SOFC) [10]
A perovskite is any material with a crystal structure following the formula ABX3, which was first discovered as the mineral called perovskite, which consists of calcium titanium oxide (CaTiO3). The mineral was first discovered in the Ural mountains of Russia by Gustav Rose in 1839 and named after Russian mineralogist L. A. Perovski (1792–1856). 'A' and 'B' are two positively charged ions (i.e. cations), often of very different sizes, and X is a negatively charged ion (an anion, frequently oxide) that bonds to both cations. The 'A' atoms are generally larger than the 'B' atoms. The ideal cubic structure has the B cation in 6-fold coordination, surrounded by an octahedron of anions, and the A cation in 12-fold cuboctahedral coordination. Additional perovskite forms may exist where either/both the A and B sites have a configuration of A1x-1A2x and/or B1y-1B2y and the X may deviate from the ideal coordination configuration as ions within the A and B sites undergo changes in their oxidation states.
Molybdenum trioxide describes a family of inorganic compounds with the formula MoO3(H2O)n where n = 0, 1, 2. The anhydrous compound is produced on the largest scale of any molybdenum compound since it is the main intermediate produced when molybdenum ores are purified. The anhydrous oxide is a precursor to molybdenum metal, an important alloying agent. It is also an important industrial catalyst. It is a yellow solid, although impure samples can appear blue or green.
In the area of solid state chemistry. graphite intercalation compounds are materials prepared by intercalation of diverse guests into graphite. The materials have the formula (guest)Cn where n can range from 8 to 40's. The distance between the carbon layers increases significantly upon insertion of the guests. Common guests are reducing agents such as alkali metals. Strong oxidants, such as arsenic pentafluoride also intercalate into graphite. Intercalation involves electron transfer into or out of the host. The properties of these materials differ from those of the parent graphite.
Indium(III) oxide (In2O3) is a chemical compound, an amphoteric oxide of indium.
Resistive random-access memory is a type of non-volatile (NV) random-access (RAM) computer memory that works by changing the resistance across a dielectric solid-state material, often referred to as a memristor. One major advantage of ReRAM over other NVRAM technologies is the ability to scale below 10nm.
Perovskite (pronunciation: ) is a calcium titanium oxide mineral composed of calcium titanate (chemical formula CaTiO3). Its name is also applied to the class of compounds which have the same type of crystal structure as CaTiO3, known as the perovskite structure, which has a general chemical formula A2+B4+(X2−)3. Many different cations can be embedded in this structure, allowing the development of diverse engineered materials.
Dichlorine hexoxide is the chemical compound with the molecular formula Cl
2O
6, which is correct for its gaseous state. However, in liquid or solid form, this chlorine oxide ionizes into the dark red ionic compound chloryl perchlorate [ClO
2]+
[ClO
4]−
, which may be thought of as the mixed anhydride of chloric and perchloric acids.
A lithium ion manganese oxide battery (LMO) is a lithium-ion cell that uses manganese dioxide, MnO
2, as the cathode material. They function through the same intercalation/de-intercalation mechanism as other commercialized secondary battery technologies, such as LiCoO
2. Cathodes based on manganese-oxide components are earth-abundant, inexpensive, non-toxic, and provide better thermal stability.
Aurivillius phases are a form of perovskite represented by the general formulae is (Bi2O2)(An−1BnO3n+1) (where A is a large 12 co-ordinate cation, and B is a small 6 co-ordinate cation).
Lanthanum manganite is an inorganic compound with the formula LaMnO3, often abbreviated as LMO. Lanthanum manganite is formed in the perovskite structure, consisting of oxygen octahedra with a central Mn atom. The cubic perovskite structure is distorted into an orthorhombic structure by a strong Jahn–Teller distortion of the oxygen octahedra.
A perovskite solar cell (PSC) is a type of solar cell that includes a perovskite-structured compound, most commonly a hybrid organic–inorganic lead or tin halide-based material as the light-harvesting active layer. Perovskite materials, such as methylammonium lead halides and all-inorganic cesium lead halide, are cheap to produce and simple to manufacture.
Methods of oxygen storage for subsequent use span many approaches, including high pressures in oxygen tanks, cryogenics, oxygen-rich compounds and reaction mixtures, and chemical compounds that reversibly release oxygen upon heating or pressure change. O2 is the second most important industrial gas.
Methylammonium lead halides (MALHs) are solid compounds with perovskite structure and a chemical formula of [CH3NH3]+Pb2+(X−)3, where X = Cl, Br or I. They have potential applications in solar cells, lasers, light-emitting diodes, photodetectors, radiation detectors, scintillator, magneto-optical data storage and hydrogen production.
Nickel forms a series of mixed oxide compounds which are commonly called nickelates. A nickelate is an anion containing nickel or a salt containing a nickelate anion, or a double compound containing nickel bound to oxygen and other elements. Nickel can be in different or even mixed oxidation states, ranging from +1, +2, +3 to +4. The anions can contain a single nickel ion, or multiple to form a cluster ion. The solid mixed oxide compounds are often ceramics, but can also be metallic. They have a variety of electrical and magnetic properties. Rare-earth elements form a range of perovskite nickelates, in which the properties vary systematically as the rare-earth element changes. Fine tuning of properties is achievable with mixtures of elements, applying stress or pressure, or varying the physical form.
A tin-based perovskite solar cell is a special type of perovskite solar cell, where the lead is substituted by tin. It has a tin-based perovskite structure (ASnX3), where 'A' is a 1+ cation and 'X' is a monovalent halogen anion. The methylammonium tin triiodide (CH3NH3SnI3) has a band gap of 1.2–1.3 eV, while formamidinium tin triiodide has a band gap of 1.4 eV.
Mixed conductors, also known as mixed ion-electron conductors(MIEC), are a single-phase material that has significant conduction ionically and electronically. Due to the mixed conduction, a formally neutral species can transport in a solid and therefore mass storage and redistribution are enabled. Mixed conductors are well known in conjugation with high-temperature superconductivity and are able to capacitate rapid solid-state reactions.
Arnold Guloy is an American chemist who is Professor of Chemistry at the University of Houston. He is an expert in the area Zintl phases chemistry, crystal growth, materials discovery, and superconductivity.
Maksym V. Kovalenko is a full professor of inorganic chemistry and the head of the Functional Inorganic Materials group at ETH Zurich. A part of the research activities of the group are conducted at Empa (Dübendorf). He is working in the fields of solid-state chemistry, quantum dots and other nanomaterials, surface chemistry, self-assembly, optical spectroscopy, optoelectronics and energy storage.
Perovskite nanocrystals are a class of semiconductor nanocrystals, which exhibit unique characteristics that separate them from traditional quantum dots. Perovskite nanocrystals have an ABX3 composition where A = cesium, methylammonium (MA), or formamidinium (FA); B = lead or tin; and X = chloride, bromide, or iodide.
Protactinium compounds are compounds containing the element protactinium. These compounds usually have protactinium in the +5 oxidation state, although these compounds can also exist in the +2, +3 and +4 oxidation states.