4.8 Review

Polymer photocatalysts for solar-to-chemical energy conversion

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NATURE REVIEWS MATERIALS
卷 6, 期 2, 页码 168-190

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NATURE PORTFOLIO
DOI: 10.1038/s41578-020-00254-z

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资金

  1. ERC Starting Grant (project COF Leaf) [639233]
  2. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [358283783-SFB 1333]
  3. Max Planck Society
  4. Center for NanoScience (CeNS)
  5. Cluster of Excellence e-conversion

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Organic polymeric photocatalysts offer a promising solution for sustainable energy resources with their precise molecular backbone and broad design space. By analyzing the photophysical and physico-chemical concepts, design principles and future research directions in the emerging field of 'soft photocatalysis' can be derived. The review discusses the fundamental concepts governing the photocatalytic performance of organic polymer photocatalysts and explores the challenges and potential future developments in the field.
Solar-to-chemical energy conversion for the generation of high-energy chemicals is one of the most viable solutions to the quest for sustainable energy resources. Although long dominated by inorganic semiconductors, organic polymeric photocatalysts offer the advantage of a broad, molecular-level design space of their optoelectronic and surface catalytic properties, owing to their molecularly precise backbone. In this Review, we discuss the fundamental concepts of polymeric photocatalysis and examine different polymeric photocatalysts, including carbon nitrides, conjugated polymers, covalent triazine frameworks and covalent organic frameworks. We analyse the photophysical and physico-chemical concepts that govern the photocatalytic performance of these materials, and derive design principles and possible future research directions in this emerging field of 'soft photocatalysis'. In this Review, the authors analyse the fundamental concepts that govern the photocatalytic performance of organic polymer photocatalysts and discuss the challenges and future of the field of 'soft photocatalysis'.

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