Abstract
Organic semiconductors have recently emerged as promising catalytic materials for oxygen reduction to hydrogen peroxide, H(2)O(2), a chemical of great importance in industry as well as biology. While examples of organic semiconductor-mediated photocatalytic and electrocatalytic processes for H(2)O(2) production become more numerous and improve in performance, fundamental understanding of the reaction mechanisms at play have been explored far less. The aim of the present work is to computationally test hypotheses of how selective oxygen reduction to H(2)O(2) generally occurs on carbonyl dyes and pigments. As an example material, we consider epindolidione (EPI), an industrial pigment with demonstrated semiconductor properties, which photocatalytic activity in oxygen reduction reaction (ORR) and thereby producing hydrogen peroxide (H(2)O(2)) in low pH environment has been recently experimentally demonstrated. In this work, the ability of the reduced form of EPI, viz. EPI-2H (which was formed after a photoinduced 2e(-)/2H(+) process), to reduce molecular triplet oxygen to peroxide and the possible mechanism of this reaction are computationally investigated using density functional theory. In the main reaction pathway, the reduction of O(2) to H(2)O(2) reaction occurs via abstraction of one of the hydrogen atoms of EPI-2H by triplet dioxygen to produce an intermediate complex consisting of the radicals of hydrogen peroxide (HOO(•)) and EPI-H(•) at the initial stage. HOO(•) thus released can abstract another hydrogen atom from EPI-H(•) to produce H(2)O(2) and regenerates EPI; otherwise, it can enter another pathway to abstract hydrogen from a neighboring EPI-2H to form EPI-H(•) and H(2)O(2). EPI, after reduction, thus plays in ORR the role of hydrogen atom transfer (HAT) agent via its OH group, similar to anthraquinone in the industrial process, while HAT from its amino hydrogen is found unfavorable.