Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720, USA.
Chem Soc Rev. 2016 Jun 7;45(11):3221-43. doi: 10.1039/c6cs00062b. Epub 2016 Apr 28.
The reduction of carbon dioxide by water with sunlight in an artificial system offers an opportunity for utilizing non-arable land for generating renewable transportation fuels to replace fossil resources. Because of the very large scale required for the impact on fuel consumption, the scalability of artificial photosystems is of key importance. Closing the photosynthetic cycle of carbon dioxide reduction and water oxidation on the nanoscale addresses major barriers for scalability as well as high efficiency, such as resistance losses inherent to ion transport over macroscale distances, loss of charge and other efficiency degrading processes, or excessive need for the balance of system components, to mention a few. For the conversion of carbon dioxide to six-electron or even more highly reduced liquid fuel products, introduction of a proton conducting, gas impermeable separation membrane is critical. This article reviews recent progress in the development of light absorber-catalyst assemblies for the reduction and oxidation half reactions with focus on well defined polynuclear structures, and on novel approaches for optimizing electron transfer among the molecular or nanoparticulate components. Studies by time-resolved optical and infrared spectroscopy for the understanding of charge transfer processes between the chromophore and the catalyst, and of the mechanism of water oxidation at metal oxide nanocatalysts through direct observation of surface reaction intermediates are discussed. All-inorganic polynuclear units for reducing carbon dioxide by water at the nanoscale are introduced, and progress towards core-shell nanotube assemblies for completing the photosynthetic cycle under membrane separation is described.
利用阳光将二氧化碳还原为水的人工系统为利用非耕地生产可再生交通燃料以替代化石资源提供了机会。由于对燃料消耗的影响规模非常大,因此人工光合作用系统的可扩展性至关重要。在纳米尺度上闭合二氧化碳还原和水氧化的光合作用循环可以解决可扩展性和高效率方面的主要障碍,例如离子在宏观距离上传输固有的电阻损耗、电荷损失和其他降低效率的过程,或者对系统组件平衡的过度需求等。对于将二氧化碳转化为六电子甚至更高还原程度的液体燃料产品,引入质子导电、气体不可渗透的分离膜是至关重要的。本文综述了用于还原和氧化半反应的光吸收剂-催化剂组件的最新进展,重点介绍了多核结构和优化分子或纳米颗粒组件之间电子转移的新方法。通过时间分辨光学和红外光谱研究,讨论了理解发色团和催化剂之间的电荷转移过程以及通过直接观察表面反应中间体来了解金属氧化物纳米催化剂上水氧化的机制。介绍了用于在纳米尺度上通过水还原二氧化碳的全无机多核单元,并描述了在膜分离下完成光合作用循环的核壳纳米管组件的进展。