Internal Electric Field Assisted Photocatalytic Generation
of Hydrogen Peroxide over BiOCl with HCOOH
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Abstract
Hydrogen peroxide
(H<sub>2</sub>O<sub>2</sub>) is a superb, clean,
and versatile reagent. However, large-scale production of H<sub>2</sub>O<sub>2</sub> is manufactured through nongreen methods that motivate
people to develop more efficient and green technologies as alternatives.
As a novel and green technology used for H<sub>2</sub>O<sub>2</sub> generation, the efficiency of photocatalysis is still far from satisfactory.
Here, we demonstrate a novel and efficient path of the generation
of H<sub>2</sub>O<sub>2</sub> in BiOCl photocatalysis but not the
direct electron reduction of O<sub>2</sub> or hole oxidation of OH<sup>–</sup> to H<sub>2</sub>O<sub>2</sub>. Super high production
(685 μmol/h) of H<sub>2</sub>O<sub>2</sub> by the addition of
HCOOH as the hole shuttle was realized over BiOCl nanoplates. In this
photocatalytic system, the BiOCl supplied abundant photoinduced holes
to initiate HCOO<sup>•</sup> radical. The HCOO<sup>•</sup> further reacts with OH<sup>–</sup> to •OH which is
proven to be the source of the H<sub>2</sub>O<sub>2</sub>. Apart from
HCOOH, O<sub>2</sub> also played important roles. The O<sub>2</sub> not only promoted the reaction through the cycle between Bi<sup>3+</sup> and Bi, which decreased the combination of carriers, but
also avoided the carbonation of surfaces, thus achieving the high
production of H<sub>2</sub>O<sub>2</sub> (1020 μmol/h). In this
work, we shed light on a deep understanding of the photocatalytic
evolution of H<sub>2</sub>O<sub>2</sub> in a novel perspective and
achieve high production