Đang chuẩn bị liên kết để tải về tài liệu:
NiSn nanoparticle-incorporated carbon nanofibers as efficient electrocatalysts for urea oxidation and working anodes in direct urea fuel cells

Đang chuẩn bị nút TẢI XUỐNG, xin hãy chờ

Synthesis of NiSn alloy nanoparticle-incorporated carbon nanofibers was performed by calcining electrospun mats composed of nickel acetate, tin chloride and poly(vinyl alcohol) under vacuum. The electrochemical measurements indicated that utilization of tin as a co-catalyst could strongly enhance the electrocatalytic activity if its content and calcination temperature were optimized. Typically, the nanofibers prepared from calcination of an electrospun solution containing 15 wt% SnCl2 at 700 C have a current density almost 9-fold higher than that of pristine nickel-incorporated carbon nanofibers (77 and 9 mA/cm2 , respectively) at 30 C in a 1.0 M urea solution. Furthermore, the current density increases to 175 mA/cm2 at 55 C for the urea oxidation reaction. Interestingly, the nanofibers prepared from a solution with 10 wt% of co-catalyst precursor show an onset potential of 175 mV (vs. Ag/AgCl) at 55 C, making this proposed composite an adequate anode material for direct urea fuel cells. Optimization of the co-catalyst content to maximize the generated current density resulted in a Gaussian function peak at 15 wt%. However, studying the influence of the calcination temperature indicated that 850 C was the optimum temperature because synthesizing the proposed nanofibers at 1000 C led to a decrease in the graphite content, which dramatically decreased the catalyst activity. Overall, the study opens a new venue for the researchers to exploit tin as effective co-catalyst to enhance the electrocatalytic performance of the nickel-based nanostructures. Moreover, the proposed co-catalyst can be utilized with other functional electrocatalysts to improve their activity toward oxidation of different fuels. | NiSn nanoparticle-incorporated carbon nanofibers as efficient electrocatalysts for urea oxidation and working anodes in direct urea fuel cells

TÀI LIỆU LIÊN QUAN