Origin and Perspectives of the Photochemical Activity of Nanoporous Carbons

被引:55
作者
Bandosz, Teresa J. [1 ,2 ]
Ania, Conchi O. [3 ,4 ]
机构
[1] CUNY, Dept Chem & Biochem, New York, NY 10031 USA
[2] CUNY, Energy Ctr, New York, NY 10031 USA
[3] Univ Orleans, CEMHTI, CNRS, UPR 3079, F-4571 Orleans, France
[4] CSIC, Inst Nacl Carbon INCAR, Oviedo 33011, Spain
关键词
bandgap; nanoporous carbons; photoactivity; photocatalysis; surface chemistry; HETEROGENEOUS PHOTOCATALYTIC OXIDATION; OXYGEN REDUCTION REACTION; C-1S CORE EXCITON; VISIBLE-LIGHT; AMORPHOUS-CARBON; METAL-FREE; ACTIVATED CARBONS; ELECTRON-TRANSFER; QUANTUM DOTS; AQUEOUS-SOLUTIONS;
D O I
10.1002/advs.201800293
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Even though, owing to the complexity of nanoporous carbons' structure and chemistry, the origin of their photoactivity is not yet fully understood, the recent works addressed here clearly show the ability of these materials to absorb light and convert the photogenerated charge carriers into chemical reactions. In many aspects, nanoporous carbons are similar to graphene; their pores are built of distorted graphene layers and defects that arise from their amorphicity and reactivity. As in graphene, the photoactivity of nanoporous carbons is linked to their semiconducting, optical, and electronic properties, defined by the composition and structural defects in the distorted graphene layers that facilitate the exciton splitting and charge separation, minimizing surface recombination. The tight confinement in the nanopores is critical to avoid surface charge recombination and to obtain high photochemical quantum yields. The results obtained so far, although the field is still in its infancy, leave no doubts on the possibilities of applying photochemistry in the confined space of carbon pores in various strategic disciplines such as degradation of pollutants, solar water splitting, or CO2 mitigation. Perhaps the future of photovoltaics and smart-self-cleaning or photocorrosion coatings is in exploring the use of nanoporous carbons.
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页数:27
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