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(a) <t>Thermogravimetric</t> curves and calculation results. (b) The Zr 3d spectrum of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (c) Zeta potential of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (d) Normalized XANES and (e) EXAFS spectra of MOF‐808 and MOF‐808‐0.11TCPP. (f) WT‐EXAFS of MOF‐808. (g) WT‐EXAFS of MOF‐808‐0.11TCPP. (h) Potentiometric acid‐base titration. (i) The coordination number of BTC, TCPP, HCOOH, and compensated ligands of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP.
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(a) <t>Thermogravimetric</t> curves and calculation results. (b) The Zr 3d spectrum of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (c) Zeta potential of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (d) Normalized XANES and (e) EXAFS spectra of MOF‐808 and MOF‐808‐0.11TCPP. (f) WT‐EXAFS of MOF‐808. (g) WT‐EXAFS of MOF‐808‐0.11TCPP. (h) Potentiometric acid‐base titration. (i) The coordination number of BTC, TCPP, HCOOH, and compensated ligands of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP.
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(a) Thermogravimetric curves and calculation results. (b) The Zr 3d spectrum of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (c) Zeta potential of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (d) Normalized XANES and (e) EXAFS spectra of MOF‐808 and MOF‐808‐0.11TCPP. (f) WT‐EXAFS of MOF‐808. (g) WT‐EXAFS of MOF‐808‐0.11TCPP. (h) Potentiometric acid‐base titration. (i) The coordination number of BTC, TCPP, HCOOH, and compensated ligands of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP.

Journal: Advanced Science

Article Title: Bioinspired Porphyrin‐Based Catalysts From Temporospatial Confined Frameworks for Ultrafast Removal of Sulfaclozine

doi: 10.1002/advs.77224

Figure Lengend Snippet: (a) Thermogravimetric curves and calculation results. (b) The Zr 3d spectrum of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (c) Zeta potential of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP. (d) Normalized XANES and (e) EXAFS spectra of MOF‐808 and MOF‐808‐0.11TCPP. (f) WT‐EXAFS of MOF‐808. (g) WT‐EXAFS of MOF‐808‐0.11TCPP. (h) Potentiometric acid‐base titration. (i) The coordination number of BTC, TCPP, HCOOH, and compensated ligands of MOF‐808, MOF‐808‐0.11TCPP, and MOF‐808‐0.21TCPP.

Article Snippet: The defect structure of the synthesized materials was described using Zeta potential (Malvern Zetasizer Nano ZS ZEN3600, UK), thermogravimetric analysis (TGA, TG‐DTA 8122, Rigaku, Japan), H Nuclear Magnetic Resonance Spectra (1H NMR, Bruker 400 MHz, Germany), X‐ray photoelectron spectroscopy (XPS, Thermo Scientific K‐Alpha, USA), electron spin resonance (ESR, Bruker EMX plus, Germany) measurements, and XANES spectra measurements.

Techniques: Zeta Potential Analyzer, Titration