State Key Laboratory of Catalysis, Collaborative Innovation Center of Chemistry for Energy Materials, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Collaborative Innovation Center of Chemistry for Energy Materials, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Nat Commun. 2019 Jan 8;10(1):86. doi: 10.1038/s41467-018-07937-w.
Traditional water-gas shift reaction provides one primary route for industrial production of clean-energy hydrogen. However, this process operates at high temperatures and pressures, and requires additional separation of H from products containing CO, CH and residual CO. Herein, we report a room-temperature electrochemical water-gas shift process for direct production of high purity hydrogen (over 99.99%) with a faradaic efficiency of approximately 100%. Through rational design of anode structure to facilitate CO diffusion and PtCu catalyst to optimize CO adsorption, the anodic onset potential is lowered to almost 0 volts versus the reversible hydrogen electrode at room temperature and atmospheric pressure. The optimized PtCu catalyst achieves a current density of 70.0 mA cm at 0.6 volts which is over 12 times that of commercial Pt/C (40 wt.%) catalyst, and remains stable for even more than 475 h. This study opens a new and promising route of producing high purity hydrogen.
传统的水气变换反应为清洁能源氢气的工业生产提供了主要途径之一。然而,该过程在高温高压下运行,并且需要从含有 CO、CH 和残余 CO 的产物中额外分离 H。在此,我们报告了一种室温电化学水气变换过程,可直接生产纯度高于 99.99%的高纯氢气,法拉第效率约为 100%。通过合理设计阳极结构以促进 CO 扩散和 PtCu 催化剂以优化 CO 吸附,将阳极起始电位降低至室温和大气压下几乎接近零伏相对于可逆氢电极。优化后的 PtCu 催化剂在 0.6 伏时实现了 70.0 mA cm 的电流密度,是商业 Pt/C(40wt.%)催化剂的 12 倍以上,甚至在 475 小时以上仍保持稳定。这项研究为生产高纯氢气开辟了一条新的、有前途的途径。