Research Center for Solar Energy Chemistry, and Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka 560-8531 (Japan).
Angew Chem Int Ed Engl. 2014 Dec 1;53(49):13454-9. doi: 10.1002/anie.201407938. Epub 2014 Oct 7.
Design of green, safe, and sustainable process for the synthesis of hydrogen peroxide (H2 O2 ) is a very important subject. Early reported processes, however, require hydrogen (H2 ) and palladium-based catalysts. Herein we propose a photocatalytic process for H2 O2 synthesis driven by metal-free catalysts with earth-abundant water and molecular oxygen (O2 ) as resources under sunlight irradiation (λ>400 nm). We use graphitic carbon nitride (g-C3 N4 ) containing electron-deficient aromatic diimide units as catalysts. Incorporating the diimide units positively shifts the valence-band potential of the catalysts, while maintaining sufficient conduction-band potential for O2 reduction. Visible light irradiation of the catalysts in pure water with O2 successfully produces H2 O2 by oxidation of water by the photoformed valence-band holes and selective two-electron reduction of O2 by the conduction band electrons.
设计绿色、安全和可持续的过氧化氢(H2O2)合成工艺是一个非常重要的课题。然而,早期报道的工艺需要氢气(H2)和基于钯的催化剂。在此,我们提出了一种在阳光照射下(λ>400nm),以金属自由催化剂、丰富的水和分子氧(O2)为资源驱动的光催化 H2O2 合成工艺。我们使用含有缺电子芳香二酰亚胺单元的石墨相氮化碳(g-C3N4)作为催化剂。二酰亚胺单元的掺入使催化剂的价带电位正向移动,同时保持足够的导带电位以还原 O2。在纯水中,用 O2 对催化剂进行可见光照射,通过光形成的价带空穴氧化水,并通过导带电子选择性地还原两电子 O2,成功地产生了 H2O2。