光催化
过氧化氢
共价键
可再生能源
合理设计
化学
纳米技术
材料科学
催化作用
选择性
组合化学
分解
人工光合作用
太阳能
可持续能源
生化工程
绿色化学
分解水
功能群
光化学
氢
可持续设计
化学稳定性
太阳能转换
析氧
计算机科学
表面改性
氧化还原
作者
Avanti Chakraborty,Pekham Chakrabortty,Pradip Pachfule
标识
DOI:10.1021/acs.chemmater.5c02292
摘要
Artificial photosynthesis offers a sustainable approach to harnessing solar energy and converting it into valuable chemical fuels. Among the renewable products, hydrogen peroxide (H2O2) has gained significant attention as a green oxidant with wide industrial and environmental applications. Nevertheless, its photocatalytic generation is constrained by the limited efficiency, stability, and selectivity of existing materials. This article presents a comprehensive overview of recent advances in methods and materials for photocatalytic H2O2 production, emphasizing how synthetic innovations and structural design have improved light absorption, charge transfer, and surface reactivity. In this perspective, the mechanistic insights into the oxygen reduction and water oxidation pathways have been discussed to clarify factors governing activity and selectivity. Particular focus is placed on covalent organic frameworks (COFs), a class of crystalline, porous, and metal-free photocatalysts with tunable architectures, extended π-conjugation, and high photochemical stability. Their emergence has enabled rational strategies such as donor–acceptor engineering, functional group incorporation, and architecture modulation to suppress H2O2 decomposition and enhance yields. Representative examples are critically evaluated to highlight strengths and limitations, while future challenges, including stability under practical conditions and scalability, are addressed. Overall, this article highlights the potential of COF-based photocatalysts in promoting solar-driven H2O2 production.
科研通智能强力驱动
Strongly Powered by AbleSci AI