The excess of mango peels is considered manufacturing waste in the sugar and juice industry. There is an increasing interest in looking for alternative ways to employ this waste to address this overload. Here, we show the efficient use of mango peels as a noncost carbon source for the synthesis of graphene. We demonstrate for the first time the synthesis of graphene on Cu substrates from mango peels, a biomass rich in pectin. It is observed that plasma presence is essential for the growth of graphene from mango peels. At 15 and 30 min of plasma exposure, we observed the presence of multilayered graphene, at longer plasma exposure, i.e., 60 min, there is the formation of monolayer graphene, attributed to the etching of multiple layers formed at short times due to long plasma exposure time. When employing this technique, precautions must be taken due to the etching effect of plasma, such as reducing either the plasma exposure time or the plasma power. Finally, we present a graphene growth pathway under plasma environment on the basis of our experimental observations.

The Haber-Bosch process has been the commercial benchmark process for ammonia synthesis for more than a century. Plasma-catalytic synthesis for ammonia production is theorized to have a great potential for being a greener alternative to the Haber-Bosch process. However, the underlying reactions for ammonia synthesis still require some detailed study especially for radiofrequency plasmas. Herein, the use of inductively coupled radiofrequency plasma for the synthesis of ammonia when employing Ga, In and their alloys as catalysts is presented. The plasma is characterized using emission spectroscopy and the surface of catalysts using Scanning Electron Microscope. A maximum energy yield of 0.31 g-NH₃/kWh and energy cost of 196 MJ/mol is achieved with Ga-In (0.6:0.4 and 0.2:0.8) alloy at 50 W plasma power. Granular nodes are observed on the surface of catalysts indicating the formation of the intermediate GaN.

The nanostructure of β-gallium oxide crystals influences the conversion to carbamates; specifically, for the synthesis of alkyl carbamates (like propyl N-octylcarbamate) from CO₂ and n-propanol in the absence of phosgene. The nanostructures with variable aspect ratios (length (L)/width (D); from 2 to 18) were prepared by the controlled addition of neutral and cationic surfactants during gallium oxide synthesis. These catalysts displayed selectivities to the corresponding carbamates as high as ~70%, superior to non-nanostructured Ga₂O₃ catalysts. The conversion was found to be inversely proportional to the square of the relative crystallinity. The catalysts retained their structure and catalytic performance upon recycling.