Li Junshan, Xing Congcong, Zhang Yu, Zhang Ting, Spadaro Maria Chiara, Wu Qianbao, Yi Yunan, He Shenglan, Llorca Jordi, Arbiol Jordi, Cabot Andreu, Cui Chunhua
Molecular Electrochemistry Laboratory, Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, 610054, P. R. China.
Catalonia Institute for Energy Research - IREC, Sant Adrià de Besòs, Barcelona, 08930, Spain.
Small. 2021 Feb;17(6):e2006623. doi: 10.1002/smll.202006623. Epub 2021 Jan 18.
The electro-oxidation of methanol to formate is an interesting example of the potential use of renewable energies to add value to a biosourced chemical commodity. Additionally, methanol electro-oxidation can replace the sluggish oxygen evolution reaction when coupled to hydrogen evolution or to the electroreduction of other biomass-derived intermediates. But the cost-effective realization of these reaction schemes requires the development of efficient and low-cost electrocatalysts. Here, a noble metal-free catalyst, Ni Fe Se nanorods, with a high potential for an efficient and selective methanol conversion to formate is demonstrated. At its optimum composition, Ni Fe Se , this diselenide is able to produce 0.47 mmol cm h of formate at 50 mA cm with a Faradaic conversion efficiency of 99%. Additionally, this noble-metal-free catalyst is able to continuously work for over 50 000 s with a minimal loss of efficiency, delivering initial current densities above 50 mA cm and 2.2 A mg in a 1.0 m KOH electrolyte with 1.0 m methanol at 1.5 V versus reversible hydrogen electrode. This work demonstrates the highly efficient and selective methanol-to-formate conversion on Ni-based noble-metal-free catalysts, and more importantly it shows a very promising example to exploit the electrocatalytic conversion of biomass-derived chemicals.
甲醇电氧化生成甲酸盐是利用可再生能源为生物源化学商品增值的一个有趣例子。此外,甲醇电氧化在与析氢或其他生物质衍生中间体的电还原耦合时,可以替代缓慢的析氧反应。但要实现这些反应方案的成本效益,需要开发高效且低成本的电催化剂。在此,展示了一种无贵金属催化剂——镍铁硒纳米棒,它在将甲醇高效且选择性地转化为甲酸盐方面具有很高潜力。在其最佳组成NiFeSe时,这种二硒化物能够在50 mA/cm²的电流密度下,以99%的法拉第转换效率产生0.47 mmol·cm⁻²·h⁻¹的甲酸盐。此外,这种无贵金属催化剂能够在1.0 m KOH电解液(含1.0 m甲醇)中,相对于可逆氢电极在1.5 V电压下,以最小的效率损失连续工作超过50000 s,初始电流密度高于50 mA/cm²且质量活性为2.2 A/mg。这项工作展示了镍基无贵金属催化剂上高效且选择性的甲醇到甲酸盐的转化,更重要的是,它为利用生物质衍生化学品的电催化转化提供了一个非常有前景的例子。