4.7 Article

Efficient photoreduction of diluted CO2 using lattice-strained Ni1_xSe nanoflowers

Journal

JOURNAL OF CO2 UTILIZATION
Volume 64, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jcou.2022.102193

Keywords

Lattice strain; NiSe nanoflowers; Diluted CO2; Photoreduction

Funding

  1. National Natural Science Foundation of China [22076049]
  2. China Postdoctoral Science Foundation [2021M701246]
  3. National Key Research and Development Program of China [2019YFC1805902, 2019YFA0210402]

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This study modulated the lattice strain in NiSe to improve the photoreduction efficiency of diluted CO2 and found that lattice strain facilitated the adsorption and activation of CO2. The results of this study are important for the design and synthesis of high-performance catalysts.
Photoreduction of diluted CO2 is an effective strategy for the sustainable and environmentally friendly development of energy. In this study, lattice strain in NiSe is modulated through the control of the Ni concentration for the photoreduction of diluted CO2. Refined XRD data and the results of the Williamson-Hall analysis indicate that the lattice strain is induced by lattice distortion caused by an absence of Ni atoms in the crystal lattice. In pure CO2, the cumulative CO yield and selectivity of Ni1-xSe nanoflowers reached approximately 19.39 mu mol and 90.7 % in 3 h, respectively. For lower CO2 concentrations of 0.1 and 0.05 atm, the CO selectivity of Ni1-xSe was approximately 72.7 % and 61.7 %, respectively. On characterization of the synthesized nanoflowers, we deduced that the lattice-strained Ni1-xSe exhibited a favorable electronic band structure that improved the separation efficiency of the photogenerated carriers. DFT calculations results revealed that the lattice strain significantly facilitated the adsorption and activation of CO2, which resulted in highly efficient CO2 photoreduction. This study provides an effective strategy for the design and synthesis of high-performance catalysts based on the modification of their crystal structures.

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