论文标题

高通量生产廉价矿物的2D电催化剂,用于高电流密度演化

High-Throughput Production of Cheap Mineral-Based 2D Electrocatalysts for High-Current-Density Hydrogen Evolution

论文作者

Zhang, Chi, Luo, Yuting, Tan, Junyang, Yang, Fengning, Zhang, Zhiyuan, Yang, Liusi, Cheng, Hui-Ming, Liu, Bilu

论文摘要

高通量可扩展的廉价,高效且耐用的电催化剂在行业所需的高电流密度上效果很好,这对于大规模实施电化学技术是一个巨大的挑战。在这里,我们报告了通过可扩展的自上而下的去角质技术的基于2D MOS2的墨水电催化剂的生产,然后进行简单的热处理。该催化剂在无需IR校正的情况下,在454 mV的超电势时显示出1000 mA CM^-2的高电流密度,并在24小时内进行良好的稳定性。使用相同的方法,我们首次产生了一种廉价的MOS2矿物基催化剂,发现它具有出色的高电流密度性能。值得注意的是,该基于MOS2的催化剂的生产速率比先前报道的催化剂高一到两个数量级。此外,MOS2矿物质的价格比商用PT催化剂低五个数量级,使MOS2矿物基催化剂便宜,并且墨水型催化剂分散剂可以轻松地与其他用于大型催化剂电极制备的技术集成。这些优势表明,作为电化学技术中的催化剂,这种方法和基于矿物质的廉价和丰富的自然资源的巨大潜力。

The high-throughput scalable production of cheap, efficient and durable electrocatalysts that work well at high current densities demanded by industry is a great challenge for the large-scale implementation of electrochemical technologies. Here we report the production of a 2D MoS2-based ink-type electrocatalyst by a scalable top-down exfoliation technique followed by a simple heat treatment. The catalyst shows a high current density of 1000 mA cm^-2 at an overpotential of 454 mV for the hydrogen evolution reaction (HER) without the need of iR correction, as well as good stability over 24 hours. Using the same method, we have, for the first time, produced a cheap MoS2 mineral-based catalyst and found that it had an excellent performance for high-current-density HER. Noteworthy, production rate of this MoS2-based catalyst is one to two orders of magnitude higher than those previously reported. In addition, the price of the MoS2 mineral is five orders of magnitude lower than commercial Pt catalysts, making the MoS2 mineral-based catalyst cheap, and the ink-type catalyst dispersions can be easily integrated with other technologies for large-scale catalyst electrode preparation. These advantages indicate the huge potentials of this method and mineral-based cheap and abundant natural resources as catalysts in the electrochemical technologies.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源