“…Among the investigated precursors, for the synthesis of PrO x , the thermal decomposition of the nitrate salt [9,11,14] and the calcination of the hydroxide [9,15,16] have been already discussed in the present paper; remaining in the same ambit, studies have been focused also on the thermal decomposition of the carbonate, either as such, Pr 2 (CO 3 ) 3 • 8H 2 O, or after a reaction with citric acid (CA), which forms a complex with the metal ion [18]. Contrary to what happens in the case of the nitrate [11], the carbonate completely loses the water of crystallization in the temperature range between 25 • C and 152 • C. Subsequently, at about 435 • C, Pr 2 O 2 CO 3 is formed, and this species remains stable for about 70 degrees, prior to the evolution of CO 2 and the consequent formation of PrO 1.833 , behind 520 • C. As far as the Pr-CA complex is concerned, its stability seems to depend on the composition of the surrounding atmosphere: in the presence of a current of oxygen, the formation of PrO 1.833 is quantitative already at 450 • C; at this temperature, but in the presence of nitrogen or in air (static conditions), Pr 2 O 2 CO 3 is the major product (while heating in air, minor amounts of PrO 1.833 are also produced).…”