4.8 Article

Multi-Level Architecture Optimization of MOF-Templated Co-Based Nanoparticles Embedded in Hollow N-Doped Carbon Polyhedra for Efficient OER and ORR

期刊

ACS CATALYSIS
卷 8, 期 9, 页码 7879-7888

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b02504

关键词

core-shell; yolk@shell; hollow; Co@Co3O4; oxygen evolution reaction; oxygen reduction reaction

资金

  1. National Natural Science Foundation of China [21436005, 21576095, 21606087]
  2. Guangdong Natural Science Funds for Distinguished Young Scholar [2018B030306050]
  3. Fundamental Research Funds for the Central Universities [2017PY004, 2017MS069]
  4. Science and Technology Program of Guangzhou [201804020009]
  5. Pearl River S&T Nova Program of Guangzhou [201806010140]
  6. State Key Laboratory of Pulp and Paper Engineering [2017ZD04, 2018TS03]
  7. Natural Science Foundation of Guangdong Province [2016A050502004, 2017A030312005]

向作者/读者索取更多资源

Emerging clean energy technologies such as regenerative fuel cells and rechargeable metal-air batteries have attracted increasing global interest because of their high efficiency and environmental benignity, but the lack of highly active bifunctional electrocatalysts at low cost for both oxygen reduction and evolution reactions (ORR and OER) greatly hinders their commercial applications. Here, we report the multilevel architecture optimization of Co-based nanoparticles (NPs) embedded in hollow N-doped carbon polyhedra for boosting the ORR and OER, which are fabricated by a two-step pyrolysis-oxidation strategy with a Co-based MOF (ZIF-67) as precursor. The key for this strategy lies in the precise and effective control of the oxidation processes of Co NPs, which enables the synthesis of a series of Co-Co3O4-based nanoarchitectures that are embedded in hollow nitrogen doped carbon polyhedra (HNCP), including core-shell Co/Co3O4, yolk@shell Co@Co3O4, and hollow Co3O4 NPs. Benefiting from its abundant oxygen vacancies and tetrahedral Co2+ and potential synergies of CoO, species and nitrogen-doped carbon as well as the efficient mass transfer of hollow and yolk-shell structures, the optimal yolk@shell Co3O4/HNCP-40 exhibits high activity for the OER with a low overpotential of 333 mV at 10 mA cm(-2) and a small Tafel slope of 69 mV dec(-1), which is better than those of commercial IrO2 (its overpotential and Tafel slope are 409 mV at 10 mA cm(-2) and 104 mV dec(-1), respectively). Meanwhile, the catalyst also exhibits comparable ORR catalytic activity with a half-wave potential of 0.834 V but better stability and methanol tolerance relative to commercial Pt/C (20 wt %), making it a potential bifunctional electrocatalyst for both the OER and ORR. This MOF-templated strategy for multilevel nanostructures provides insights into the development of highly efficient and low-cost bifunctional electrocatalysts for the OER/ORR.

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