Now, while various catalysts are currently used for CO₂conversion reactions, most of them were designed and investigated for use in high-temperature and -pressure conditions. This is a serious limitation for multiple reasons. First, maintaining such conditions requires energy and expensive containment systems. Second, the CO₂hydrogenation reaction is exothermic, and thus proceeds more favorably at lower temperatures. Third, high temperatures can sometimes compromise the stability of catalysts, resulting in their reduced lifespan. Finally, the conversion efficiency of existing heterogenous catalysts is extremely low for catalyzing such conversion reactions.

Against this backdrop, a team of researchers led by Professor Hideo Hosono from Tokyo Institute of Technology, Japan, set out to develop a better catalyst for CO₂hydrogenation. In their study published in theJournal of the American Chemical Society, they report the development of a novel intermetallic catalyst synthesized via a simple ammonolysis process by combining palladium (Pd) and molybdenum (Mo).

To synthesize this catalyst, the researchers employed a simple approach based on ammonolysis of an oxide precursor. Put simply, ammonolysis can be used to combine metals by mixing precursors, such as oxides or nitrates, with ammonia gas at high temperatures. Ammonia reacts with the precursors to form intermediate complexes called metal amides, which then decompose to form the desired intermetallic compound.

Using various analytical techniques, the team determined the crystal structure of the "h-PdMo" catalyst and probed its chemical and thermal stability. Notably, they found that h-PdMo was stable at temperatures up to 400 °C and did not decompose in air. "This kind of robustness is very important when considering the practicality of a catalyst," remarks Prof. Hosono.

Next, the researchers evaluated the performance of h-PdMo for CO₂hydrogenation under different conditions. At a temperature of 100 °C, the catalyst was capable of continuous methanol production without any significant sign of degradation, for over 100 hours. Moreover, at room temperature (25 °C) and under relatively low pressure, the performance of h-PdMo was remarkable. Explaining the findings further, Prof. Hosono says, "At a pressure of 0.9 MPa, our catalyst achieved a conversion efficiency comparable to or even higher than that of state-of-the-art heterogeneous catalysts, that demonstrate similar turn over efficiency under higher-pressure conditions in the range of 4 to 5 MPa."

总之,研究人员开发了一个非常活性e and stable catalyst for CO₂hydrogenation at room temperature that can be synthesized via a simple process. Prof. Hosono concludes by saying, "Our discovery provides a frontier for catalyst development, not only for low-temperature methanol synthesis and CO₂conversion reactions, but also for other reactions catalyzed by Pd."