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Strategy of Graphdiyne (g-Cn H2n-2 ) Preparation Coupling with the Flower-Like NiAl-LDH Heterojunctions for Efficient Photocatalytic Hydrogen Evolution*.
Jin, Zhi-Liang; Wang, Yuan-Peng.
Afiliação
  • Jin ZL; School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan, 750021, P. R.China.
  • Wang YP; Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan, 750021, P. R.China.
Chemistry ; 27(49): 12649-12658, 2021 Sep 01.
Article em En | MEDLINE | ID: mdl-34180095
ABSTRACT
Graphdiyne (g-Cn H2n-2 ), a novel two-dimension carbon allotrope material composed of a sp- and sp2 -hybrid carbon network, has been widely explored since it was synthesized for the first time by Li's group in 2010. A series distinct and excellent properties bestow graphdiyne excellent performance in many fields. Here, an innovative progress for preparing graphdiyne by using Cu+ contained material as catalyst is reported and the composite CuI-GD is coupled with flower-like NiAl-LDH to produce H2 from photocatalytic water splitting. The results of FTIR and Raman spectroscopy together reveal that graphdiyne nanosheets are synthesized successfully by employing a cross-coupling method. Photocatalytic hydrogen evolution performance shows that the hydrogen production activity of CuI-GD/NiAl-LDH has a 15- and 216-fold enhancement compared with CuI-GD and NiAl-LDH, respectively. A series of characterizations are carried out to expound the underlying reasons in the enhancement of the photocatalytic hydrogen production performance of CuI-GD/NiAl-LDH. Meanwhile, a possible mechanism for the photocatalytic hydrogen evolution process was proposed to understand the interaction among these materials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2021 Tipo de documento: Article