The Cover shows that N
2O from plant can be effectively decomposed into N
2 and O
2 over a series of Co-Ti oxides. In their Full Paper, C. Zhang et al. show that deactivation occurred over time for the Co
3O
4 catalyst, however, Co
0.6Ti maintained nearly 100 % N
2O conversion for at least 30 h. Moreover, the Co
0.6Ti catalyst showed much stronger resistance against 1.5 vol. % O
2, 2.4 vol. % H
2O, or 1.6 vol. % NO in the feed compared with the Co
3O
4 catalyst. The existence of a strong interaction between Co and Ti oxides in the Co
xTi catalysts is thought to be the reason, leading to a larger BET specific surface area and better structural stability than the Co
3O
4 catalyst. The deactivation of the Co
3O
4 catalyst is attributed to even weaker structural stability, leading to the decrease in the amount of surface Co
3+. More information can be found in the Full Paper by C. Zhang et al. on
page 2155 in Issue 12, 2016 (DOI:
10.1002/cctc.201600231).