糠醇
光催化
化学
联轴节(管道)
酰胺
能量转移
光化学
酒
有机化学
材料科学
催化作用
分子物理学
冶金
作者
Liangpang Xu,K.S. Yeung,Lejing Li,Xixian Nan,Aleksandr Savateev,Zhuofeng Hu,Jimmy C. Yu
标识
DOI:10.1002/ange.202504635
摘要
Photocatalytic oxygen reduction provides a sustainable approach for hydrogen peroxide (H2O2) synthesis, but the charge carrier‐based pathway is severely limited by inefficient charge separation and redox decomposition of the produced H2O2. Energy transfer photocatalysis (EnTP) is an alternative charge‐carrier‐free route for H2O2 synthesis. Herein, we propose a strategy of killing two birds with one stone to simultaneously realize the synthesis of H2O2 and conversion of a biomass derivative by coupling EnTP with the Achmatowicz reaction. Results show efficient production of H2O2 at a rate of 14.6 mmol gcat‐1 h−1 and an apparent quantum yield of 44.1% at 420 nm, coupled with the conversion of biomass‐derived furfuryl alcohol (FFA) to hydroxy‐2H‐pyran‐3(6H)‐one with a high selectivity of 85.9%. Such a performance was attributed to the efficient EnTP over the amide‐functionalized heptazine framework photocatalyst for singlet oxygen generation, which induces the FFA conversion and concurrently produces H2O2. A systematic study of the photoexcitation process of the catalysts reveals that the amide‐functionalization significantly improves the intersystem crossing efficiency, as the structural modification optimizes the electronic structure and thus tunes the composition and distribution of energy bands.
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