Abstract
In a recent <i>Nature Catalysis</i> paper, Müller and coworkers engineer Cu/Mo<sub>2</sub>C<i>T</i><sub>x</sub> (MXene) interface and achieve high intrinsic methanol formation rate and selectivity. Due to the good mobility of Cu species under H<sub>2</sub> at 500°C and increased electron affinity of partially reduced Mo<sub>2</sub>C<i>T</i><sub>x</sub> surface, the interface of Cu/Mo<sub>2</sub>C<i>T</i><sub>x</sub> becomes strong Lewis acid as reduction time increases, which correlates with enhanced rate of CO<sub>2</sub> hydrogenation to methanol.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
