A nontraditional approach to the development of catalysts for low-temp
erature ammonia synthesis is considered. The approach is characterized
by application of catalysts representing heterogeneous analogs of the
known homogeneous nitrogen-fixing systems based on transition metal c
ompounds and strong electron donors. The use of this approach led to t
he development of catalysts that considerably surpass in their activit
y (at atmospheric pressure) the industrial catalyst for the ammonia sy
nthesis. Some of the developed catalysts are active in the formation o
f ammonia from dinitrogen and dihidrogen even at 110-150 degrees C. Th
e mechanisms of activation and hydrogenation of dinitrogen over these
new catalysts are discussed.