Multifunctional oxides offer huge potential for technological
applications,
owing to their inclusive physical properties such as ferroelectric,
piezoelectric, and electro-caloric properties. The natural occurrence
of piezoelectricity, a tunable band gap of ferroelectrics, opens a
path to study the light–material interaction, leading to photoconduction
and photovoltaic effects. Such light-controlled devices yield additional
advantages of weight reduction and wireless, remote-controlled functionality
over the heavy electric circuitry and, hence, are projected as an
alternative solution to the traditional piezoelectric-based devices.
Among these materials, lead-free BaTiO3-based ferroelectric
materials are a good choice for their potential applications with
recently discovered light-controlled functionality. However, until
now, the coupling of light with the chemistry of ferroelectricity
of BaTiO3 crystals has been elusive, although the ferroelectricity
and piezoelectricity are well-studied. Here, the present study reports
the photostrictive effect of the order of 10–4 on
the dimension of the c domains of tetragonal BaTiO3 crystals and domain reorientation at room temperature under
unpolarized, coherent visible light illumination, consequently resulting
in enhancement in polarization. The electronic origin of domain evolution
and photostriction is explained by the light-induced modification
in the Ti 3d–O 2p-hybridized orbitals. This facilitates the
perspective of combining mechanical, electrical, optical, and functionalities
in future generations of remote-controlled devices.