Atomic tuning on cobalt enables an eightfold increase of H2O2 production

That explains why hydrogen peroxide (H₂O₂), a major electronic cleaning chemical, is one of the most valuable chemical feedstock that underpins the chip-making industry. Despite the ever-growing significance of H₂O₂, its industry has been left with an energy-intensive and multi-step method known as the anthraquinone process. This is an environmentally unfriendly process which involves the hydrogenation step using expensive palladium catalysts. Alternatively, H₂O₂ can be synthesized directly from H2 and O2 gas, although the reactivity is still very poor and it requires high pressure. Another eco-friendly method is to electrochemically reduce oxygen to H₂O₂ via 2-electron pathway. Recently, noble metal-based electrocatalysts (for example, Au-Pd, Pt-Hg, and Pd-Hg) have been demonstrated to show H₂O₂ productivity although such expensive investment has seen low returns that fails to meet the scalable industry needs.

Researchers at the Center for Nanoparticle Research (led by Director Taeghwan HYEON and Vice Director Yung-Eun SUNG) within the Institute for Basic Science (IBS) in collaboration with Professor Jong Suk YOO at University of Seoul recently report an ultimate electrocatalyst that addresses all of the issues that trouble H₂O₂ production. This new catalyst comprising the optimal Co-N4 molecules incorporated in nitrogen-doped graphene, Co1-NG(O), exhibits a record-high electrocatalytic reactivity, producing up to 8 times higher the amount of H₂O₂ that can be generated from rather expensive noble metal-based electrocatalysts (for example, Pt, Au-Pd, Pt-Hg and so on). The synthesized catalysts entirely comprise at least 2000 times less expensive elements (Co, N, C, and O) than the conventional palladium catalyst, and they are exceptionally stable without activity loss over 110 hours of H₂O₂ production.

Typically involving different phases of catalysts (usually solid) and reactants (gas), heterogeneous catalysts are widely exploited in many important industrial processes. Still, their catalytic property was thought to be controlled only by changing the constituent elements. In this study, the researchers verified that they can induce a specific interaction on heterogeneous catalysts by fine-tuning the local atomic configurations of the elements as seen in enzyme catalysts. Director Hyeon, the corresponding author of the study notes, "this study successfully demonstrated the possibility of controlling a catalytic property by tuning atomic compositions. This finding may bring us closer to discovering the fundamental properties of catalytic activities."

Based on the theoretical analysis, it was verified that the charge density of a cobalt atom on a nitrogen-doped graphene is highly dependent on the coordination structure surrounding the cobalt atom. Therefore, the researchers could control electron density of cobalt atoms by introducing either electron-rich or electron-poor species such as oxygen or hydrogen atoms. When electron-rich oxygen atoms are nearby, Co atoms become electron-deficient. On the other hand, when electron-rich hydrogen atom is nearby, the opposite trend was found (which would generate electron-rich Co atoms). Very interestingly, the electron density of Co atoms were critical for the electrochemical H₂O₂ production.

Next, the researchers designed the optimal cobalt atomic structure (Co1¬-N4(O)) by having all of the required conditions such as precise selection of element, synthesis temperature and various experimental conditions met. Combining theoretical simulations and nanomaterial synthesis technologies, the researchers were able to control the catalytic property in atomic precision. With electron-poor Co atoms (Co1-NG(O)), they were able to produce H₂O₂ with significantly high activity and stability, far surpassing the state-of-the-art noble metal catalysts. Conversely, electron-rich Co atoms exhibited a high reactivity for 4-electron oxygen reduction reaction to H₂O formation which might be found useful for fuel cell applications.

Surprisingly, 341.2 kg of H₂O₂ can be produced within 1 day at room temperature and atmospheric pressure using 1 kg of Co1-NG(O) catalyst. This amount of H₂O₂ is up to 8 times higher the amount of H₂O₂ produced by the state-of-the-art noble metal catalysts. Co1-N4(O)) is an ultimate catalyst that allows low-cost, efficient, and eco-friendly production of H₂O₂. Professor Sung, the corresponding author says, "For the first time, we found that the catalytic property of heterogeneous catalysts can be fine-tuned in atomic precision. This unprecedented result will help us to understand previous unknown aspects of electrochemical H₂O₂ production. With this knowledge, we could design a scalable catalyst that is entirely composed of earth-abundant elements (Co, N, C, and O)."