Single-photon emitters
in hexagonal boron nitride (h-BN) exhibit
compelling optical properties, such as high brightness and photostability,
making them promising candidates for applications in emerging nanophotonic
and quantum technologies. However, their further progress would greatly
benefit from the identification of their chemical nature, which in
most cases is still under debate. Among the various emitters observed
in h-BN, blue quantum emitters (435 nm), also known as B-centers,
are unique not only due to their promising optical properties but
also because they can be fabricated at specific locations via electron-beam
irradiation. Herein, ab initio calculations are used
to demonstrate that the properties of a carbon chain tetramer are
in excellent agreement with the characteristics of blue quantum emitters.
The calculated zero-phonon line (ZPL) energy (3.13 eV) and radiative
lifetime (1.62 ns) of the carbon chain tetramer align well with experimental
observations. The relatively weak electron–phonon coupling
indicates intense emission at the ZPL, and the Debye–Waller
factor of 0.25 is consistent with experimental data. We demonstrate
that, despite the absence of an inversion center in the carbon chain
tetramer, it exhibits a negligible linear Stark effect, consistent
with experimental findings. Additionally, our hypothesis explains
the experimental observation that the formation of blue emitters is
only possible in samples containing numerous ultraviolet emitters,
which are probably identical to carbon dimers.