the crystallographic structures of the patterns, a Bruker AXS D8 X-ray
powder diffractometer with a simple cubic lattice and CU Kα
radiation (λ = 0.15406 nm) was used, and the scan range (2θ)
changing 5–90° was implemented. Fourier transform infrared
spectroscopy (FTIR, Spectrum Two, PerkinElmer, USA) was applied to
probe the structure and chemical bonds of the molecule. The Raman
spectrum was investigated using a Raman microscope (Alpha 300 M+,
WITec, Germany). The morphology of the patterns was screened using
a field-emission scanning electron microscope (FESEM, Gemini 550)
and a scanning transmission electron microscope (STEM, Gemini 550).
Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda
methods were used to analyze the pore size distribution, total pore
volume (TPV), and the specific surface area (SSA) of the patterns.