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Internal Electric Field Assisted Photocatalytic Generation of Hydrogen Peroxide over BiOCl with HCOOH

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

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The Francis Crick Institute

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Last time updated on 13/08/2018

This paper was published in The Francis Crick Institute.

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