Carbon nanomaterials are in high demand owing to their exceptional physical and chemical properties. This study employed a mixture of CH₄, H₂, and N₂ to create carbon nanostructures on a single-crystal diamond using microwave plasma chemical vapor deposition (MPCVD) under high-power conditions. By controlling the substrate surface and nitrogen flow rate, carbon nanowires, carbon nanotubes, and carbon pompons could be selectively deposited. The results obtained from OES, SEM, TEM, and Raman spectroscopy revealed that the nitrogen flow rate and substrate surface conditions were crucial for the growth of carbon nanostructures. The changes in the plasma shape enhanced the etching effect, promoting the growth of carbon pompons. The CN and C₂ groups play vital catalytic roles in the formation of carbon nanotubes and nanowires, guiding the precipitation and composite growth of carbon atoms at the interface between the Mo metal catalysts and diamond. This study demonstrated that heterostructures of diamond–carbon nanomaterials could be produced under high-power conditions, offering a new approach to integrating diamond and carbon nanomaterials.

A novel cyanide-free gold electroplating bath was developed with 2-hydroxyphosphonoacetic acid (HPAA) as the core complexing agent in this work. Scanning electron microscopy (SEM) observations demonstrate that the obtained gold electrodeposits possess a smooth and compact surface morphology. The crystal structure of the gold electrodeposits was characterized via X-ray diffraction (XRD), and the coating–substrate adhesion was systematically evaluated through scratch tests. Molecular dynamics (MD) simulations were performed to investigate the adsorption interaction between HPAA and metal (Au/Ni) surfaces. The MD simulation results show that all the studied phosphonate-containing derivatives can strongly adsorb on the gold surface and exert a significant inhibitory effect on the electroreduction of gold ions during electrodeposition. Cyclic voltammetry (CV) and other electrochemical tests reveal that the cathodic reduction peak potential of gold shifts significantly negatively after the addition of phosphonate-based organic additives, which effectively enhances the cathodic polarization of gold deposition, delays the gold nucleation rate, and refines the grain size of electrodeposits, ultimately yielding gold electrodeposits with a denser and smoother surface. Owing to its environmental benignity, excellent process stability and superior coating performance, this cyanide-free gold electroplating system exhibits broad application prospects in the field of modern green surface engineering.