Zhou Qiansong, Zhang Meng, Zhu Beien, Gao Yi
Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Nanomaterials (Basel). 2022 Jul 25;12(15):2557. doi: 10.3390/nano12152557.
Single atom catalysts (SACs) have received a lot of attention in recent years for their high catalytic activity, selectivity, and atomic utilization rates. Two-dimensional N-doped graphene has been widely used to stabilize transition metal (TM) SACs in many reactions. However, the anchored SAC could lose its activity because of the too strong metal-N interaction. Alternatively, we studied the stability and activity of dual-atom catalysts (DACs) for 24 TMs on N-doped graphene, which kept the dispersion state but had different electronic structures from SACs. Our results show that seven DACs can be formed directly compared to the SACs. The others can form stably when the number of TMs is slightly larger than the number of vacancies. We further show that some of the DACs present better catalytic activities in hydrogen evolution reaction (HER) than the corresponding SACs, which can be attributed to the optimal charge transfer that is tuned by the additional atom. After the screening, the DAC of Re is identified as the most promising catalyst for HER. This study provides useful information for designing atomically-dispersed catalysts on N-doped graphene beyond SACs.
近年来,单原子催化剂(SACs)因其高催化活性、选择性和原子利用率而备受关注。二维氮掺杂石墨烯已被广泛用于在许多反应中稳定过渡金属(TM)单原子催化剂。然而,由于金属 - 氮相互作用过强,锚定的单原子催化剂可能会失去活性。另外,我们研究了24种过渡金属在氮掺杂石墨烯上的双原子催化剂(DACs)的稳定性和活性,其保持了分散状态,但具有与单原子催化剂不同的电子结构。我们的结果表明,与单原子催化剂相比,可直接形成七种双原子催化剂。当过渡金属的数量略大于空位数量时,其他双原子催化剂可以稳定形成。我们进一步表明,一些双原子催化剂在析氢反应(HER)中表现出比相应单原子催化剂更好的催化活性,这可归因于由额外原子调节的最佳电荷转移。经过筛选,铼双原子催化剂被确定为最有前途的析氢反应催化剂。这项研究为设计除单原子催化剂之外的氮掺杂石墨烯上的原子分散催化剂提供了有用信息。