In plain words

Light changing colour as it passes through a material. Normally a material responds in proportion to the light falling on it, and the colour stays the same. With intense light, such as a laser pulse, part of the response follows the square or the cube of the light’s field, and new colours appear: light at twice or three times the frequency, or pairs of split from one. Thin layers convert little simply because they are thin, but some are so strongly nonlinear for their thickness that they are studied as chip-sized frequency converters and sources of entangled photons.

As the site uses it

The device interest is a naturally polar, chemically stable semiconductor for compact nonlinear optics and photodetection.

RhSeCl, RhTeCl · Rhodium chalcohalides

The mixed bonding breaks symmetries that simpler compounds keep, giving polar Janus semiconductors, giant spin splitting, ferroelectric layers, exceptionally strong nonlinear optics and layered photocatalysts.

The materials

Going deeper

Three panels. New colours: a laser at frequency ω enters a crystal, and light at ω, 2ω and 3ω leaves it. Which crystals double it: NbOI₂ gives both 2ω and 3ω, while TaOI₂ gives only 3ω. One photon into two: a pump photon enters a thin layer and two photons leave it in different directions, joined by a dashed line marking them as an entangled pair. new colours ω ω 2ω 3ω light at 2ω and 3ω intense light gets a response in its square and its cube new colours from one laser which crystals double it NbOI₂ 2ω 3ω TaOI₂ 3ω no 2ω the square needs broken symmetry, the cube does not: only NbOI₂ doubles the frequency a test of symmetry, too one photon into two pump a thin layer an entangled pair one photon splits into two, born together, entangled a microscopic quantum source
Intense light drives a response in the square and the cube of its field, and new frequencies appear. The square term needs a crystal without a centre of inversion – only ferroelectric NbOI2, not TaOI2, doubles the frequency – while the cube term does not. Run backwards, the square term splits one photon into an entangled pair.

Beyond proportional

In everyday optics the electrons of a material follow the light’s electric field in step, and the light that comes out has the colour that went in. Push harder, with the field of a focused laser pulse, and the response gains parts that grow with the square and the cube of the field. Those parts oscillate at twice and three times the light’s frequency, so a material lit at 1560 nm can give light at 780 and at 520 nm.

The square term needs a crystal without a centre of inversion – in a symmetric crystal it cancels – which is why doubles as a test of symmetry. The cube term has no such condition. Of the oxide iodides NbOI2 and TaOI2, only NbOI2 gives second-harmonic light, while both give third-harmonic light about as efficiently as a of WS2, growing as the square of the thickness up to about 30 nm (Tang and colleagues, 2024).

Thin but strong

Conversion builds up as light travels through a crystal, as long as the light it generates keeps in step with the light that makes it; over a coherence length, often a few micrometres, the two drift apart and the gain reverses – the reason bulk converters need phase matching. A layer a few nanometres thick never gets that far, so it needs no phase matching at all, but it also has almost no length to convert in, and its output stays small.

Some layered crystals are so strongly nonlinear for their thickness that the trade is still attractive, and stacking can recover part of the length: in twisted stacks of -MoS2 arranged so that the generated light keeps adding up, frequency doubling and photon-pair generation were both enhanced (Tang and colleagues, 2024). Bulk crystals of the same family are already in use: GaSe is an established crystal for generating radiation and converting infrared light.

Pairs of photons

Run backwards, the square term splits one photon into two of lower energy, born together – spontaneous parametric down-conversion, the standard source of entangled photons. Thin layers make such a source microscopic. boron nitride, free of the strong light emission that limits 2D , gave more than 120 coincident pairs per second, with a coincidence-to-accidental ratio above 200, entangled in polarisation, with the entangled state chosen by turning the pump’s polarisation (Liang and colleagues, 2025).

Ferroelectric layers add a possible switch: their second-order response follows their polarisation, so reversing it electrically could reverse the response – one of the open questions for the oxide .

For specialists

Optical response beyond linear order in the field, P = ε0(χ(1)E + χ(2)E2 + χ(3)E3 + …). Second-order processes – second-harmonic and sum-frequency generation, spontaneous parametric down-conversion – need symmetry; third-order ones – third-harmonic generation, the optical – occur in any material. Layers much thinner than the coherence length need no phase matching but convert weakly; stacking can compensate, as in twisted 3R-MoS2 stacks that quasi-phase-match frequency doubling and photon-pair generation. Rhombohedral BN, free of the that limits 2D semiconductors, gives polarisation-entangled photon pairs whose Bell state is set by the pump polarisation.

Where this comes from

  1. Third harmonic generation in thin NbOI2 and TaOI2 Tang et al. · Nanomaterials 14, 412 (2024) cited by 17
  2. Quasi-phase-matching enabled by van der Waals stacking Tang et al. · Nature Communications 15, 9979 (2024)
  3. Tunable polarization entangled photon-pair source in rhombohedral boron nitride Liang et al. · Science Advances 11, eadt3710 (2025)

In the news

The newest items in the site’s news feed that use the term, one from each source.

Journal Nano Letters

Nonlinear Optical Fingerprints of Defects in Hexagonal Boron Nitride

Hexagonal boron nitride (h-BN) defects are promising building blocks for quantum and , yet their nonlinear optical signatures remain poorly understood. We use calculations to determine the polarization-resolved linear, second-order, and third-order susceptibilities of multilayer h-BN…

ExperimentTheoryhBN
Journal Advanced Functional Materials

Optical Signature of Moiré Superlattices Formed by Twisted SrTiO3 Membranes

formed at the interfaces of mismatched lattices have attracted significant interest over the past decade due to their large tunability of band parameters and interactions among electrons, , and lattices. Superlattices made from twisted perovskite oxides may have strong structure and potential…

Experiment

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