异质结
材料科学
光催化
分解水
氮化碳
碳纤维
堆积
过氧化氢
硼
催化作用
制氢
光化学
化学工程
纳米技术
化学
光电子学
复合数
有机化学
工程类
复合材料
作者
Yong Guo,Xudong Miao,Xueyang Zhang,Huinan Che,Ying Li
标识
DOI:10.1016/j.seppur.2023.124807
摘要
The development of novel metal-free catalysts to photosynthesize hydrogen peroxide (H2O2) is recognized as a prospective technology for sustainable energy conversion. Herein, the carbon-doped boron nitride (BCN) and perylene tetracarboxylic dianhydride (PTCDA) formed PDA@BCN S-scheme heterojunctions with π-π stacking, which catalyzed the production of H2O2 at an unexpectedly high yield of 285.47 μmol h-1 g-1 in air. The high photocatalytic performance is attributed to the enhanced light absorption resulting in abundant carrier excitation, rapid charge separation driven by S-scheme heterojunctions, and highly selective H2O2 formation pathway. Theoretical calculations demonstrate that carbon sites in PDA@BCN can serve as an advanced active center for oxygen enrichment and activation, promoting oxygen reduction and efficient photocatalytic production of H2O2. This work lays the foundation for the design of efficient, stable, and reusable photocatalysts for environmental restoration and energy conversion.
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