A copper (Cu) material is catalytically active for formaldehyde (HCHO) dehydrogenation to produce H, 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 generation from HCHO aqueous solution at room temperature. Under the optimized reaction conditions, the CuNi@C catalyst exhibits a H evolution rate of 110.98 mmol·h·g, 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 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 generation results from the synergistic contribution between the massive active species from HCHO decomposition on the Cu sites and the remarkable H 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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.1c11776 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!