4.8 Article

A CuNi Alloy-Carbon Layer Core-Shell Catalyst for Highly Efficient Conversion of Aqueous Formaldehyde to Hydrogen at Room Temperature

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 31, Pages 37289-37297

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c11776

Keywords

dehydrogenation; formaldehyde; CuNi alloy catalyst; carbon layer; hydrogen generation

Funding

  1. National Natural Science Foundation of China [22078118, 21972048, 21802046]
  2. Guangdong Basic and Applied Basic Research Foundation [2021A1515010349, 2019A1515011138, 2018A0303130018]
  3. Guangzhou Basic and Applied Basic Research Foundation [202102080166]

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Alloying with other metals and coating a carbon layer outside can improve the efficiency and durability of copper catalysts for formaldehyde dehydrogenation to produce hydrogen, making them promising catalysts for energy recovery from industrial formaldehyde wastewater.
A copper (Cu) material is catalytically active for formaldehyde (HCHO) dehydrogenation to produce H-2, but the unsatisfactory efficiency and easy corrosion hinder its practical application. Alloying with other metals and coating a carbon layer outside are recognized as effective strategies to improve the catalytic activity and the long-term durability of nonprecious metal catalysts. Here, highly dispersed CuNi alloy-carbon layer core-shell nanoparticles (CuNi@C) have been developed as a robust catalyst for efficient H-2 generation from HCHO aqueous solution at room temperature. Under the optimized reaction conditions, the CuNi@C catalyst exhibits a H-2 evolution rate of 110.98 mmol.h(-1).g(-1), which is 1.5 and 4.9 times higher than those of Cu@C and Ni@C, respectively, which ranks top among the reported nonprecious metal catalysts for catalytic HCHO reforming at room temperature to date. Furthermore, CuNi@C also displays excellent stability toward the catalytic HCHO reforming into H-2 in tap water owing to the well-constructed carbon sheath protecting CuNi nanocrystals from oxidation in an alkaline medium. Combined with density functional theory calculations, the superior catalytic efficiency of CuNi@C for H-2 generation results from the synergistic contribution between the massive active species from HCHO decomposition on the Cu sites and the remarkable H-2 evolution activity on Ni sites. The improved performance of CuNi@C highlights the enormous potential of advancing noble-metal-free nanoalloys as cost-effective and recyclable catalysts for energy recovery from industrial HCHO wastewater.

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