Graphene, mechanically exfoliated as a single-atom-thick two-dimensional (2D) material, is renowned for its exceptional carrier mobility and mechanical strength, making it a highly promising material for a wide range of applications; however, following the synthesis of large-area, high-quality graphene, quality degradation, such as tearing, frequently occurs during the transfer process. Currently, chemical vapor deposition (CVD) enables reliable synthesis of large-area graphene, and both wet and dry transfer methods are widely employed to transfer graphene onto various substrates. This study focuses on the wet transfer method to improve transfer efficiency by optimizing the interfacial adhesion among graphene, the polymethyl methacrylate (PMMA) support layer, and the target substrate. To enhance the efficiency of the wet transfer process, the PMMA concentration and ultraviolet ozone (UVO) treatment time were systematically optimized. As a result, a transfer yield of up to 97.16 % was achieved under optimized conditions consisting of 6 % PMMA concentration and 15 min of UVO exposure. This research contributes to the development of highly efficient graphene transfer techniques, which are crucial for reducing production costs and processing time in a wide range of advanced applications such as electronics, energy storage, biomedical devices, environmental monitoring, and materials science.

Cu-Ni-P alloy nano powders were fabricated by the electrical explosion of electroless Ni plated Cu wires. The effect of applied voltage on the explosion was examined by applying pulse voltage of 6 and 28 kV, The estimated overheating factor, K, were 1.3 for 6 kV and 2.2 for 28 kV. The powders produced with pulse voltage of 6 kV were composed of Cu-rich solid solution, Ni-rich solid solution, and phase. While, those produced with 28 kV were complete Cu-Ni-P solid solution and small amount of phase. The initial P content of 6.5 at.% was reduced to 2-3 at.% during explosion due to its high vapour pressure.

Cu-Zn alloy nano powders were fabricated by the electrical explosion of Zn-electroplated Cu wire along with commercial brass wire. The powders exploded from brass wire were composed mainly of phases while those from electroplated wires contained additional Zn-rich phases as , and Zn. In case of Zn-elec-troplated Cu wire, the mixing time of the two components during explosion might not be long enough to solidify as the phases of lower Zn content. This along with the high vapor pressure of Zn appears to be the reason for the observed shift of explosion products towards the high-Zn phases in electroplated wire system.