4.8 Article

Ni-Co Bimetallic Hydroxide Nanosheet Arrays Anchored on Graphene for Adsorption-Induced Enhanced Photocatalytic CO2 Reduction

Journal

ADVANCED MATERIALS
Volume 34, Issue 28, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202202960

Keywords

adsorption; catalytic reduction; CO; (2) photoreduction; hydroxide nanosheet arrays; Ni-Co bimetal

Funding

  1. National Key R&D Program of China [2020YFC1808401]
  2. National Natural Science Foundation of China [22078213, 21938006, 51973148, 21776190]
  3. cutting-edge technology basic research project of Jiangsu [BK20202012]
  4. Prospective application research project of Suzhou [SYG202042]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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This study presents a new strategy for photocatalytic CO2 reduction by designing nanocomposites with abundant active sites structures. The constructed catalyst exhibits excellent CO2 adsorption capacity and charge-carrier separation and transfer, leading to highly improved catalytic performance.
Photocatalytic CO2 reduction can be implemented to use CO2, a greenhouse gas, as a resource in an energy-saving and environmentally friendly way, in which suitable catalytic materials are required to achieve high-efficiency catalysis. Insufficient accessible active sites on the catalyst surface and inhibited electron transfer severely limit the photocatalytic performance. Therefore, porous aerogels are constructed from composites comprising different ratios of Ni-Co bimetallic hydroxide (NixCoy) grown on reduced graphene oxide (GR) into a hierarchical nanosheet-array structure using a facile in situ growth method. Detailed characterization shows that this structure exposes numerous active sites for enhanced adsorption-induced photocatalytic CO2 reduction. Moreover, under the synergistic effect of Ni-Co bimetallic hydroxide, the CO2 adsorption capacity as well as charge-carrier separation and transfer are excellent. As a result, the Ni7Co3-GR catalyst exhibits highly improved catalytic performance when compared with recently reported values, with a high CO release rate of 941.5 mu mol h(-1) g(-1) and a selectivity of 96.3% during the photocatalytic reduction of CO2. This work demonstrates a new strategy for designing nanocomposites with abundant active sites structures.

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