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Direct growth of uniform carbon nitride layers with extended optical absorption towards efficient water-splitting photoanodes.


ABSTRACT: A general synthesis of carbon nitride (CN) films with extended optical absorption, excellent charge separation under illumination, and outstanding performance as a photoanode in water-splitting photoelectrochemical cells is reported. To this end, we introduced a universal method to rapidly grow CN monomers directly from a hot saturated solution on various substrates. Upon calcination, a highly uniform carbon nitride layer with tuned structural and photophysical properties and in intimate contact with the substrate is obtained. Detailed photoelectrochemical and structural studies reveal good photoresponse up to 600?nm, excellent hole extraction efficiency (up to 62%) and strong adhesion of the CN layer to the substrate. The best CN photoanode demonstrates a benchmark-setting photocurrent density of 353?µA?cm-2 (51% faradaic efficiency for oxygen), and external quantum yield value above 12% at 450?nm at 1.23?V versus RHE in an alkaline solution, as well as low onset potential and good stability.

SUBMITTER: Qin J 

PROVIDER: S-EPMC7499157 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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Direct growth of uniform carbon nitride layers with extended optical absorption towards efficient water-splitting photoanodes.

Qin Jiani J   Barrio Jesús J   Peng Guiming G   Tzadikov Jonathan J   Abisdris Liel L   Volokh Michael M   Shalom Menny M  

Nature communications 20200917 1


A general synthesis of carbon nitride (CN) films with extended optical absorption, excellent charge separation under illumination, and outstanding performance as a photoanode in water-splitting photoelectrochemical cells is reported. To this end, we introduced a universal method to rapidly grow CN monomers directly from a hot saturated solution on various substrates. Upon calcination, a highly uniform carbon nitride layer with tuned structural and photophysical properties and in intimate contact  ...[more]

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