4.8 Article

Anchoring strategy for highly active copper nanoclusters in hydrogenation of renewable biomass-derived compounds

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 299, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120651

Keywords

Biomass transformation; Hydrogenation reaction; Cu nanocluster catalysts; Nanoconfined catalysis; Graphitic carbon nitride

Funding

  1. National Natural Science Foundation of China(NSFC) [21978137, 21878162]
  2. Natural Science Foundation of Tianjin [20JCZDJC00770]
  3. NCC Fund [NCC2020FH05]
  4. Fundamental Research Funds for the Central Universities
  5. Nankai University

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This study presents an efficient strategy for anchoring highly active copper nanocluster catalysts on graphitic carbon nitride and dispersing in mesoporous silica, resulting in high conversion of levulinic acid to γ-valerolactone with excellent stability. The research provides a simple anchoring strategy for constructing highly active and inexpensive copper nanocluster catalysts, which exhibit comparable performance to Ru/AC catalysts but more economically favorable.
The hydrogenation of levulinic acid (LA) to.-valerolactone (GVL) is a common reaction that is critical to biomass transformation. However, it is a great challenge to employ non-noble metal catalysts in realizing highly effective conversion from LA to GVL. Herein, we report an efficient strategy for anchoring highly active copper nanocluster catalysts on the defect sites of graphitic carbon nitride (g-C3N4) and dispersing in mesoporous silica (SBA15). The combination of g-C3N4 and SBA-15 stabilized the copper clusters, leading to a high GVL yield of 92 % and excellent stability in 100 h. This result is comparable to that of the Ru/AC catalyst but much more economically favorable. Density functional theory calculations revealed that the reaction barrier of the new catalyst was reduced from 1.93 to 1.12 eV compared with those of unconfined copper particles. This research provides a simple anchoring strategy for constructing highly active and inexpensive copper nanocluster catalysts.

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