Nacre (/ˈneɪkər/ NAY-kər, also /ˈnækrə/ NAK-rə), also known as mother-of-pearl, is an organic–inorganic composite material produced by some molluscs as an inner shell layer. It is also the material of which pearls are composed. It is strong, resilient, and iridescent.

Nacre is found in some of the most ancient lineages of bivalves, gastropods, and cephalopods. However, the inner layer in the great majority of mollusc shells is porcellaneous, not nacreous, and this usually results in a non-iridescent shine, or more rarely in non-nacreous iridescence such as flame structure as is found in conch pearls.

The outer layer of cultured pearls and the inside layer of pearl oyster and freshwater pearl mussel shells are made of nacre. Other mollusc families that have a nacreous inner shell layer include marine gastropods such as the Haliotidae, the Trochidae and the Turbinidae.

Nacre is composed of hexagonal platelets, called tablets, of aragonite (a form of calcium carbonate) 10–20 μm wide and 0.5 μm thick arranged in continuous parallel lamina. Depending on the species, the shape of the tablets differs; in Pinna, the tablets are rectangular, with symmetric sectors more or less soluble. Whatever the shape of the tablets, the smallest units they contain are irregular rounded granules. These layers are separated by sheets of organic matrix (interfaces) composed of elastic biopolymers (such as chitin, lustrin and silk-like proteins).

Nacre appears iridescent because the thickness of the aragonite platelets is close to the wavelength of visible light. These structures interfere constructively and destructively with different wavelengths of light at different viewing angles, creating structural colours.

The crystallographic c-axis points approximately perpendicular to the shell wall, but the direction of the other axes varies between groups. Adjacent tablets have been shown to have dramatically different c-axis orientation, generally randomly oriented within ~20° of vertical. In bivalves and cephalopods, the b-axis points in the direction of shell growth, whereas in the monoplacophora it is the a-axis that is inclined this way.

This mixture of brittle platelets and the thin layers of elastic biopolymers makes the material strong and resilient, with a Young's modulus of 70 GPa and a yield stress of roughly 70 MPa (when dry). Strength and resilience are also likely to be due to adhesion by the "brickwork" arrangement of the platelets, which inhibits transverse crack propagation. This structure, spanning multiple length sizes, greatly increases its toughness, making it almost as strong as silicon. The mineral–organic interface results in enhanced resilience and strength of the organic interlayers. The interlocking of bricks of nacre has large impact on both the deformation mechanism as well as its toughness. Tensile, shear, and compression tests, Weibull analysis, nanoindentation, and other techniques have all been used to probe the mechanical properties of nacre. Theoretical and computational methods have also been developed to explain the experimental observations of nacre's mechanical behavior. Nacre is stronger under compressive loads than tensile ones when the force is applied parallel or perpendicular to the platelets. As an oriented structure, nacre is highly anisotropic and as such, its mechanical properties are also dependent on the direction.

A variety of toughening mechanisms are responsible for nacre's mechanical behavior. The adhesive force needed to separate the proteinaceous and the aragonite phases is high, indicating that there are molecular interactions between the components. In laminated structures with hard and soft layers, a model system that can be applied to understand nacre, the fracture energy and fracture strength are both larger than those values characteristic of the hard material only. Specifically, this structure facilitates crack deflection, since it is easier for the crack to continue into the viscoelastic and compliant organic matrix than going straight into another aragonite platelet. This results in the ductile protein phase deforming such that the crack changes directions and avoids the brittle ceramic phase. Based on experiments done on nacre-like synthetic materials, it is hypothesized that the compliant matrix needs to have a larger fracture energy than the elastic energy at fracture of the hard phase. Fiber pull-out, which occurs in other ceramic composite materials, contributes to this phenomenon. Unlike in traditional synthetic composites, the aragonite in nacre forms bridges between individual tablets, so the structure is not only held together by the strong adhesion of the ceramic phase to the organic one, but also by these connecting nanoscale features. As plastic deformation starts, the mineral bridges may break, creating small asperities that roughen the aragonite-protein interface. The additional friction generated by the asperities helps the material withstand shear stresses. In nacre-like composites, the mineral bridges have also been shown to increase the flexural strength of the material because they can transfer stress in the material. Developing synthetic composites that exhibit similar mechanical properties as nacre is of interest to scientists working on developing stronger materials. To achieve these effects, researchers take inspiration from nacre and use synthetic ceramics and polymers to mimic the "brick-and-mortar" structure, mineral bridges, and other hierarchical features.