Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering , East China Normal University , Shanghai 200062 , P. R. China.
State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics , Chinese Academy of Sciences , Shanghai 200050 , P. R. China.
ACS Appl Mater Interfaces. 2018 Aug 1;10(30):25422-25428. doi: 10.1021/acsami.8b06948. Epub 2018 Jul 23.
Hydrogen (H) is presently one of the most promising clean and renewable energy sources, but the conventional hydrogen production by electrochemical water-splitting, though of great potential and extensively studied, is seriously obstructed especially by the anodic oxygen evolution reaction because of its sluggish kinetics. Herein, we report the efficient hydrogen production from methanol solution using facile-synthesized ultrathin 2D bi-metal-organic framework nanosheets (UMOFNs) as a precious metal-free anodic catalyst. The prepared UMOFNs showed a much lowered anodic potential of 1.365 (V vs reversible hydrogen electrode) at 10 mA cm, which was markedly 232 mV lower than that in conventional water splitting, and moreover, the average turnover frequency reached 19.62 s. Benefiting from nearly 100% Faraday efficiency of H production on the counter graphite carbon electrodes without additional electrocatalysts, high-purity hydrogen was produced with enhanced efficiency. More importantly, the anodic electro-reaction mechanism has been evidenced experimentally: the electrocatalytic hydrogen production from the methanol solution is a methanol-assisted water splitting, rather than a methanol-reforming process as claimed in a number of literature studies, in which methanol is oxidized as a sacrificing agent in place of water oxidization in pure water.
氢气(H)是目前最有前途的清洁可再生能源之一,但通过电化学水分解生产氢气虽然具有很大的潜力并且已经得到广泛研究,但由于动力学缓慢,其阳极析氧反应受到严重阻碍。在此,我们报告了使用简便合成的超薄二维双金属有机框架纳米片(UMOFNs)作为无贵金属的阳极催化剂,从甲醇溶液中高效生产氢气。所制备的 UMOFNs 在 10 mA cm 下的阳极电位低至 1.365(V 与可逆氢电极相比),明显低于传统水分解中的 232 mV,而且平均转化率频率达到 19.62 s。得益于在没有额外电催化剂的情况下,石墨碳对电极上 H 生产的近 100%法拉第效率,提高了生产效率。更重要的是,已经通过实验证实了阳极电反应机制:甲醇溶液中的电催化制氢是甲醇辅助的水分解,而不是许多文献研究中所声称的甲醇重整过程,其中甲醇作为牺牲剂被氧化,而不是在纯水中氧化水。