Catalysis for CO2 Hydrogenation—What We Have Learned/Should Learn from the Hydrogenation of Syngas to Methanol

Abstract

This short review provides an in-depth analysis of the achievements and further developments of the catalytic hydrogenation of carbon dioxide (CO2) to methanol from those that are worth learning about based on the transformation of syngas into methanol. We begin by exploring the environmental and energy-related implications of utilizing CO2 as a feedstock for methanol production by emphasizing its potential to mitigate greenhouse gas emissions and facilitate renewable energy integration. Then, different catalytic formulations focusing on precious metals, copper-based catalysts, and metal oxides are summarized, and insights into their advantages and limitations in the aspects of catalytic activity, selectivity, and stability are discussed. Precious metal catalysts, such as platinum and iridium, exhibit high activity but are cost-prohibitive, while copper-based catalysts present a promising and cost-effective alternative. Metal oxides are considered for their unique properties in CO2 activation. Mechanistic insights into reaction pathways are explored, with a particular emphasis on copper-based catalysts. Moreover, the complex steps involved in CO2 hydrogenation to methanol are discussed to shed light on the key intermediates and active sites responsible for catalysis, which is crucial for catalyst design and optimization. Finally, we stress the importance of ongoing research and development efforts to enhance catalyst efficiency, mechanistic comprehension, and process optimization. This review serves as a valuable resource for researchers, engineers, and policymakers working toward a more sustainable and carbon-neutral energy future. By harnessing CO2 as a carbon feedstock for methanol synthesis, we have the potential to address environmental concerns and advance the utilization of renewable energy sources, further contributing to the transition to a cleaner and more sustainable energy landscape.