4.6 Article

Ni-Co hydroxide nanosheets on plasma-reduced Co-based metal-organic nanocages for electrocatalytic water oxidation

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 7, 期 9, 页码 4950-4959

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ta00070d

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资金

  1. National Natural Science Foundation of China [21878047, 21676056, 51673040]
  2. Graduate student scientific research innovation program of Jiangsu Province [KYCX18_0132]
  3. Scientific Research Foundation of Graduate School of Southeast University [YBPY1880]
  4. Six Talents Pinnacle Program'' of Jiangsu Province of China [JNHB-006]
  5. Qing Lan Project of Jiangsu Province [1107040167]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) [1107047002]
  7. Australian Research Council

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Development of highly efficient and low-cost electrocatalysts for the oxygen evolution reaction (OER) with high electrical conductivity and chemical stability is critical for various energy conversion devices and systems, yet still remains a formidable challenge. Herein, we develop a novel porous 3D hybrid nanostructure decorated with nickel cobalt layered double hydroxides (NiCo LDHs) on the surface of the functional ZIF-67 template with rich oxygen vacancies (V-O) etched by O-2-Ar radio frequency (RF) plasma. The as-prepared NiCo LDH@ZIF-67-V-O/NF hybrid materials exhibit excellent OER performance evidenced by the competitive potential of 1.52 V at the current density of 10 mA cm(-2) in alkaline medium. Moreover, the Tafel slope of 58 mV dec(-1) is much lower compared to that of noble metal oxide and other counterpart catalysts. Our experimental and theoretical calculation results reveal that incorporation of V-O into the NiCo LDH@ZIF-67-V-O/NF composite can efficiently tune the electronic structure and also increase the water adsorption energy, ultimately accelerating the OER process. The work presents a novel strategy for designing highly efficient composite electrode materials with rich oxygen vacancies for the effective, scalable electrocatalytic water oxidation.

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