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Hydrogen Production from Formic Acid by In Situ Generated Ni/CdS Photocatalytic System under Visible Light Irradiation.
Feng, Kai-Wen; Li, Yang.
Afiliação
  • Feng KW; State Key Laboratory of Multiphase Flow in Power Engineering and Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, 710054, Shaanxi, P. R. China.
  • Li Y; State Key Laboratory of Multiphase Flow in Power Engineering and Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, 710054, Shaanxi, P. R. China.
ChemSusChem ; 16(9): e202202250, 2023 May 05.
Article em En | MEDLINE | ID: mdl-36705939
ABSTRACT
Simple and practical noble-metal-free catalyzed hydrogen production from sustainable resources, such as renewable formic acid, is highly desirable. Herein, the development of an efficient photocatalytic hydrogen production from aqueous solution of formic acid using in situ generated Ni/CdS photocatalytic system was described. CdS-Cys (Cys=l-cysteine) quantum dots (QDs) acting as photocatalyst with Ni(OAc)2 as H2 production catalyst precursor, a 94 % yield was obtained within 5 h under visible light irradiation at 50 °C. The average rate of H2 production reached up to 282 µmol mg-1 h-1 with 99.8 % H2 selectivity. Mechanistic studies indicate cooperation of dynamic quenching and static quenching of CdS-Cys QDs by Ni(OAc)2 . Especially, Ni0 , generated in the dynamic quenching, accelerated the electron transfer by acting as an electron outlet and enhancing the stability of CdS to slow down the photocorrosion distinctly, delivering efficient H2 production with high selectivity. Our study will inspire exploration of various efficient non-noble-metal catalysts for practical H2 production from bio-based formic acid.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: ChemSusChem Assunto da revista: QUIMICA / TOXICOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: ChemSusChem Assunto da revista: QUIMICA / TOXICOLOGIA Ano de publicação: 2023 Tipo de documento: Article