Room-temperature electrochemical water–gas shift reaction for high purity hydrogen production
Water-gas shift reaction
DOI:
10.1038/s41467-018-07937-w
Publication Date:
2019-01-02T17:00:44Z
AUTHORS (16)
ABSTRACT
Abstract 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, requires additional separation H 2 from products containing CO , CH 4 residual CO. Herein, we report a room-temperature electrochemical direct purity hydrogen (over 99.99%) with faradaic efficiency approximately 100%. Through rational design anode structure to facilitate diffusion PtCu catalyst optimize adsorption, the anodic onset potential is lowered almost 0 volts versus reversible electrode room temperature atmospheric pressure. The optimized achieves current density 70.0 mA cm −2 0.6 which over 12 times that commercial Pt/C (40 wt.%) catalyst, remains stable even more than 475 h. This study opens new promising producing
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