4.8 Article

Nitrogen/Carbon-Coated Zero-Valent Copper as Highly Efficient Co-catalysts for TiO2 Applied in Photocatalytic and Photoelectrocatalytic Hydrogen Production

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 27, 页码 30365-30380

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c06880

关键词

carbon-coated copper; nanoparticles; photocatalytic hydrogen production; photoelectrochemical hydrogen evolution; titanium dioxide; solvothermal synthesis

资金

  1. Alexander von Humboldt Foundation
  2. Deutscher Akademischer Austauschdienst (DAAD)
  3. Ministerio de Educacion, Cultura, Cienciay Tecnologia (Argentina)
  4. Welsh Government [80708]
  5. Innovate UK [EP/N020863/1]
  6. EPSRC [EP/R016666/1, EP/S001336/1]
  7. EPSRC [EP/S001336/1, EP/M028267/1, EP/R016666/1, EP/N020863/1] Funding Source: UKRI

向作者/读者索取更多资源

Zero-valent copper (Cu-0) is a promising co-catalyst in semiconductor-based photocatalysis as it is inexpensive and exhibits electronic properties similar to those of Ag and Au. However, its practical application in photocatalytic hydrogen production is limited by its susceptibility to oxidation, forming less active Cu species. Herein, we have carried out in situ encapsulation of Cu-0 nanoparticles with N-graphitic carbon layers (14.4% N) to stabilize Cu-0 nanoparticles (N/C-coated Cu) and improve the electronic communication with a TiO2 photocatalyst. A facile solvothermal procedure is used to coat the Cu-0 nanoparticles at 200 degrees C, while graphitization is achieved by calcination at 550 degrees C under an inert atmosphere. The resultant N/C-coated Cu/TiO2 composites outperform the uncoated Cu counterparts, exhibiting a 27-fold enhancement of the hydrogen evolution rate compared to TiO2 and achieving a rate of 19.03 mmol g(-1) h(-1) under UV-vis irradiation. Likewise, the N/C-coated Cu co-catalyst exhibits a less negative onset potential of -0.05 V toward hydrogen evolution compared to uncoated Cu (ca. -0.30 V). This superior activity is attributed to coating Cu-0 with N/C, which enhances the stability, electronic communication with TiO2, conductivity, and interfacial charge transfer processes. The reported synthetic approach is simple and scalable, yielding an efficient and affordable Cu-0 co-catalyst for TiO2.

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