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High-throughput screening of transition metal single atom catalysts anchored on molybdenum disulfide for nitrogen fixation

机译:锚定金属单原子催化剂的高通量筛选用于氮固定的二氧化钼

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Single atom catalysts (SACs) have recently been intensively explored for electrochemical nitrogen reduction reaction (NRR) because of the 100% utilization, high activity and high selectivity, in which N-doped substrates are widely used to support the SACs. Herein, we show that monolayer molybdenum disulfide (MoS2) is a potential alternative substrate to anchor transition metal (TM) SACs towards NRR. Through the first-principles high-throughput screening, we find that the single molybdenum atom (Mo) anchored on top of the Mo site of MoS2 (Mo@MoS2-M) has the best NRR performance among Ag, Au, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pd, Pt, Rh, Ru, Sc, Ti, V, W and Zn. The estimated overpotential of Mo@MoS2-M is around 0.28 V via the distal mechanism. Our results further confirm the stability of the Mo@MoS2-M as well as its good selectivity to NRR against hydrogen evolution reaction. These results pave a way to explore the new single atom-substrate pair towards high-performance nitrogen reduction.
机译:最近已经集中探索了单个原子催化剂(SAC),用于电化学氮气还原反应(NRR),因为100%利用率,高活性和高选择性,其中N掺杂的基材被广泛用于支撑囊。 在此,我们表明单层钼二硫化物(MOS2)是潜在的替代基底,以朝向NRR锚定过渡金属(TM)囊。 通过第一原理的高通量筛选,我们发现锚定的单一钼原子(Mo)在MOS2(MO @ MOS2-M)的顶部锚定,具有AG,Au,Co,Cr的最佳NRR性能, Cu,Fe,Mn,Mo,Ni,Pd,Pt,Rh,Ru,Sc,Ti,V,W和Zn。 MO @ MOS2-M的估计过电位通过远端机构约为0.28V。 我们的结果进一步证实了MO @ MOS2-M的稳定性以及对NRR的良好选择性免于氢化反应。 这些结果铺平了一种探讨了新的单个原子衬底对朝向高性能氮气减少的方法。

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