Metal-organic framework-based nanomaterials for CO₂ storage: A review

• Ha Huu Do,
• Iqra Rabani and
• Hai Bang Truong

Beilstein J. Nanotechnol. 2023, 14, 964–970, doi:10.3762/bjnano.14.79

• , including pore size manipulation, post-synthetic modifications, and composite formation. Finally, the extant challenges and anticipated prospects pertaining to the development of MOF-based nanomaterials for CO2 storage are described. Keywords: CO2 storage; metal-organic frameworks; nanomaterials; open

• [16][17][18][19]. However, several studies have indicated that the surface area is not the sole determining factor in CO2 storage at low pressure. For instance, despite having a lower surface area than MOF-177, HKUST-1 exhibited a greater CO2 adsorption capacity of 4.16 mmol·g−1 at 298 K and 1 bar [20

• different kinetic diameters of gas molecules. Herein, we present a comprehensive examination of the current scientific literature pertaining to the utilization of metal-organic framework (MOF)-based nanomaterials in the context of CO2 storage and conversion. This account focuses on the introduction of MOFs

Ni, Co, Zn, and Cu metal-organic framework-based nanomaterials for electrochemical reduction of CO₂: A review

• Ha Huu Do and
• Hai Bang Truong

Beilstein J. Nanotechnol. 2023, 14, 904–911, doi:10.3762/bjnano.14.74

• human energy consumption [2][3], this method proves instrumental in abating the pollution caused by CO2. Nevertheless, CO2 storage and transportation are expensive, necessitating the development of efficient adsorbents [3]. An auspicious avenue to tackle these challenges is the conversion of CO2 into

Playing with covalent triazine framework tiles for improved CO₂ adsorption properties and catalytic performance

• Giulia Tuci,
• Andree Iemhoff,
• Housseinou Ba,
• Lapo Luconi,
• Andrea Rossin,
• Vasiliki Papaefthimiou,
• Regina Palkovits,
• Jens Artz,
• Cuong Pham-Huu and
• Giuliano Giambastiani

Beilstein J. Nanotechnol. 2019, 10, 1217–1227, doi:10.3762/bjnano.10.121

• -dicyanoimidazole (DCI) or its equimolar mixtures with the aforementioned dicyanoaryl units (see Scheme 1 below) [45]. The as-prepared samples have been investigated as CO2 storage materials as well as metal-free catalysts for the gas-phase DDH of EB to ST. Notably, mixed CTF samples from this series have shown CO2

• , the pore volume of CTF5 is higher than that of CTF4 while the N loading is smaller; this translates in comparable Qst values for the two mixed samples (Table 2, entries 4 and 5). Overall, Qst values measured for CTF samples from this series fall in the ideal range for CO2 storage materials (<40 kJ·mol