4.8 Article

Defect-Rich Hierarchical Porous UiO-66(Zr) for Tunable Phosphate Removal

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 19, Pages 13209-13218

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c01723

Keywords

metal-organic frameworks; monocarboxylic acids; defect chemistry; hierarchical pores; phosphate removal

Funding

  1. National Natural Science Foundation of China [51878023]
  2. Beijing Natural Science Foundation [8202016]
  3. Great Wall Scholars Training Program Project of Beijing Municipality Universities [CITTCD20180323]
  4. Beijing Talent Project [2019A22]
  5. Fundamental Research Funds for the Central Universities [CUSF-DH-D-2020072]
  6. JST-ERATO Yamauchi Materials Space-Tectonics Project [JPMJER2003]
  7. Graduate Student Innovation Fund of Donghua University [CUSF-DH-D-2020072]

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The study introduced defects into hierarchical porous metal-organic frameworks (HP-MOFs) to improve their phosphate adsorption performance, using a template-assisted strategy to control the defects. Experimental results demonstrated the critical role of defect sites in enhancing phosphate uptake performance, providing a promising route for tailoring the adsorption performance of MOF-based adsorbents through defect engineering.
The introduction of defects into hierarchical porous metal-organic frameworks (HP-MOFs) is of vital significance to boost their adsorption performance. Herein, an advanced template-assisted strategy has been developed to fine-tune the phosphate adsorption performance of HP-MOFs by dictating the type and number of defects in HP-UiO-66(Zr). To achieve this, monocarboxylic acids of varying chain lengths have been employed as template molecules to fabricate an array of defect-rich HP-UiO-66(Zr) derivatives following removal of the template. The asprepared HP-UiO-66(Zr) exhibits a higher sorption capacity and faster sorption rate compared to the pristine UiO-66(Zr). Particularly, the octanoic acid-modulated UiO-66(Zr) exhibits a high adsorption capacity of 186.6 mg P/g and an intraparticle diffusion rate of 6.19 mg/g.min(0.5), which are 4.8 times and 1.9 times higher than those of pristine UiO-66(Zr), respectively. The results reveal that defect sites play a critical role in boosting the phosphate uptake performance, which is further confirmed by various advanced characterizations. Density functional theory (DFT) calculations reveal the important role of defects in not only providing additional sorption sites but also reducing the sorption energy between HP-UiO-66(Zr) and phosphate. In addition, the hierarchical pores in HP-UiO-66(Zr) can accelerate the phosphate diffusion toward the active sorption sites. This work presents a promising route to tailor the adsorption performance of MOF-based adsorbents via defect engineering.

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