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Atomic-level tuning of Co-N-C catalyst for high-performance electrochemical H_2O_2 production

机译:Co-N-C催化剂的原子级调谐,用于高性能电化学H_2O_2的生产

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摘要

Despite the growing demand for hydrogen peroxide it is almost exclusively manufactured by the energy-intensive anthraqui-none process. Alternatively, H_2O_2 can be produced electrochemically via the two-electron oxygen reduction reaction, although the performance of the state-of-the-art electrocatalysts is insufficient to meet the demands for industrialization. Interestingly, guided by first-principles calculations, we found that the catalytic properties of the Co-N_4 moiety can be tailored by fine-tuning its surrounding atomic configuration to resemble the structure-dependent catalytic properties of metalloenzymes. Using this principle, we designed and synthesized a single-atom electrocatalyst that comprises an optimized Co-N_4 moiety incorporated in nitrogen-doped graphene for H_2O_2 production and exhibits a kinetic current density of 2.8 mA cm~(-2) (at 0.65 V versus the reversible hydrogen electrode) and a mass activity of 155 Ag~(-1) (at 0.65 V versus the reversible hydrogen electrode) with negligible activity loss over 110 hours.
机译:尽管对过氧化氢的需求不断增长,但它几乎完全是通过耗能大的无蒽醌法生产的。可选择地,尽管最先进的电催化剂的性能不足以满足工业化的要求,但是可以通过双电子氧还原反应以电化学方式生产H_2O_2。有趣的是,在第一性原理计算的指导下,我们发现Co-N_4部分的催化性质可以通过微调其周围原子构型来调整,以类似于金属酶的结构依赖性催化性质。利用这一原理,我们设计并合成了一种单原子电催化剂,该催化剂包含优化的Co-N_4部分(掺入氮掺杂的石墨烯中用于生产H_2O_2),并具有2.8 mA cm〜(-2)的动电流密度(在0.65 V与(可逆氢电极)和155 Ag〜(-1)的质量活度(相对于可逆氢电极为0.65 V),在110小时内的活性损失可忽略不计。

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