4.8 Article

Single Transition Metal Atom Bound to the Unconventional Phase of the MoS2 Monolayer for Catalytic Oxygen Reduction Reaction: A First-Principles Study

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 15, 页码 17412-17419

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c21597

关键词

first-principles calculations; single-atom catalysts; oxygen reduction reaction; unconventional phase; MoS2

资金

  1. Scientific and Technological Research Program of Chongqing Municipal Education Commission [KJQN202000629]
  2. Natural Science Foundation of Chongqing [cstc2020jcyj-msxmX0692, cstc2020jcyj-msxmX0686]
  3. Fundamental Research Funds for the Central Universities [2020CDJ-LHZZ-073]

向作者/读者索取更多资源

Single-atom catalysts (SACs) have high atom utilization and excellent catalytic performance but face challenges in stability. Utilizing defect-free MoS2 monolayer in unconventional phase 1T' can effectively immobilize single TM atoms and screening out efficient ORR catalysts with low overpotential. Adsorption energy of ORR intermediate *OH and d-band center of supported TM adatoms are key factors for designing stable and high-performance SACs.
Supported single-atom catalysts (SACs) have received a lot of attention due to their super-high atom utilization and outstanding catalytic performance. However, the instability of the supported transition-metal (TM) atoms hampers their widespread applications. Exploration of an appropriate substrate to stabilize the supported single atom is crucial for the future implementation of SACs. In recent years, two-dimensional materials have been proposed as possible substrates due to their large specific surface areas, but their chemically inert surfaces are difficult to stabilize TM atoms without defecting or doping. Herein, by means of systematic first-principles calculations, we demonstrate that the defect-free MoS2 monolayer in the unconventional phase (1T') can effectively immobilize single TM atoms owing to its unique electrophilic property as compared to the conventional 2H phase. As a prototype probe, we investigated oxygen reduction reaction (ORR) catalyzed by a total of 21 single TM atoms stabilized on 1T'-MoS2 and successfully screened out two candidates, Cu and Pd@1T'-MoS2, which have a low overpotential of 0.41 and 0.32 V respectively, outperforming most of the previously reported ORR catalysts. Furthermore, we reveal that the adsorption energy of the ORR intermediate, *OH, provides an excellent descriptor to assess the ORR activity, which is further determined by the d-band center of the supported TM adatoms, thus being a great advantage for future design of stable and high-performance SACs.

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