Abstract
Efficient catalysts for the electroreduction of N
2
to NH
3
are of paramount importance for sustainable ammonia production. Recently, it was reported that NbSe
2
nanosheets exhibit an excellent catalytic activity for nitrogen reduction under ambient conditions. However, existing theoretical calculations suggested an overpotential over 3.0 V, which is too high to interpret the experimental observations. To reveal the underlying mechanism of the high catalytic activity, in this work, we assessed NbSe
2
edges with different chirality and Se vacancies by using first principles calculations. Our results show that N
2
can be efficiently reduced to NH
3
on a pristine zigzag edge
via
the enzymatic pathway with an overpotential of 0.45 V. Electronic structure analysis demonstrates that the N
2
molecule is activated by the back-donation mechanism. The efficient tuning of the local chemical environments by edge chirality provides a promising approach for catalyst design.
The zigzag edge of the NbSe
2
monolayer exhibits an overpotential as low as 0.45 V along the enzymatic pathway.