Abstract:Catalysts of oxygen reduction reaction (ORR)play key roles in renewable energy technologies such as metal-air batteries and fuel cells. Despite tremendous efforts, highly active catalysts with low cost remain elusive. This work used metal-organic frameworks to synthesize non-precious bimetallic carbon nanocomposites as efficient ORR catalysts. Although carbon-based Cu and Ni are good candidates, the hybrid nanocomposites take advantage of both metals to improve catalytic activity. The resulting molar ratio of … Show more
“…To improve the performance of ZIFs as anode materials for LIBs, we focus our attention on bimetallic ZIF to utilize the synergistic effect of two metal centers inspired by our previous work [16,[27][28][29]. To demonstrate the effectiveness of our bimetallic ZIF, we also synthesize the isostructural Zn-ZIF-8 and Co-ZIF-67 under a similar solvothermal approach by using 2-methylimidazole as the linker.…”
In this work, a bimetallic zeolitic imidazolate framework (ZIF) CoZn-ZIF was synthesized via a facile solvothermal approach and applied in lithium-ion batteries. The as-prepared CoZn-ZIF shows a high reversible capacity of 605.8 mA h g −1 at a current density of 100 mA g −1 , far beyond the performance of the corresponding monometallic Co-ZIF-67 and Zn-ZIF-8. Ex-situ synchrotron soft X-ray absorption spectroscopy, X-ray diffraction, and electron paramagnetic resonance techniques were employed to explore the Li-storage mechanism. The superior performance of CoZn-ZIF over Co-ZIF-67 and Zn-ZIF-8 could be mainly attributed to lithiation and delithiation of nitrogen atoms, accompanied by the breakage and recoordination of metal nitrogen bond. Morever, a few metal nitrogen bonds without recoordination will lead to the amorphization of CoZn-ZIF and the formation of few nitrogen radicals.
“…To improve the performance of ZIFs as anode materials for LIBs, we focus our attention on bimetallic ZIF to utilize the synergistic effect of two metal centers inspired by our previous work [16,[27][28][29]. To demonstrate the effectiveness of our bimetallic ZIF, we also synthesize the isostructural Zn-ZIF-8 and Co-ZIF-67 under a similar solvothermal approach by using 2-methylimidazole as the linker.…”
In this work, a bimetallic zeolitic imidazolate framework (ZIF) CoZn-ZIF was synthesized via a facile solvothermal approach and applied in lithium-ion batteries. The as-prepared CoZn-ZIF shows a high reversible capacity of 605.8 mA h g −1 at a current density of 100 mA g −1 , far beyond the performance of the corresponding monometallic Co-ZIF-67 and Zn-ZIF-8. Ex-situ synchrotron soft X-ray absorption spectroscopy, X-ray diffraction, and electron paramagnetic resonance techniques were employed to explore the Li-storage mechanism. The superior performance of CoZn-ZIF over Co-ZIF-67 and Zn-ZIF-8 could be mainly attributed to lithiation and delithiation of nitrogen atoms, accompanied by the breakage and recoordination of metal nitrogen bond. Morever, a few metal nitrogen bonds without recoordination will lead to the amorphization of CoZn-ZIF and the formation of few nitrogen radicals.
“…These are crystalline materials consisting of metal ions or clusters and organic linker(s) with strong covalent bonds [6,7]. Due to their high porosity, large internal surface area, and high thermal stability (generally >300°C) [7], MOFs have a variety of potential applications in many fields including gas storage [8], catalysis [9,10], drug delivery [11], and chemical sensing [12][13][14]. The intrinsic ultra-high porosity of MOFs may lead to a low RI of MOF materials.…”
The preparation and development of novel optical thin films are of great importance to functional optical and opto-electric components requiring a low refractive index. In this study, a typical metal-organic framework (MOF), MIL-101(Cr), is selected as the research model. The corresponding MOF nanoparticles are prepared by a hydrothermal method and the optical thin films are successfully prepared by spincoating. The optical properties of the corresponding MOF thin films are controlled by changing the type of functional groups on the benzene ring of the ligand (terephthalic acid) on MOFs. The functional groups are hydrogen atoms (H), electron donating groups (-NH 2, -OH) and electron withdrawing groups (-NO 2, -(NO 2 ) 2 or F 4 ), respectively. It is found that the effective refractive index (n eff ) of MOF thin films decreases along with the increasing voids among MOF nanoparticles. In addition, the extinction coefficient (k) increases with the addition of electron donating groups, and decreases with the addition of electron withdrawing groups. Among the MOFs used in this study, the n eff of NO 2 -MIL-101(Cr) containing electron withdrawing groups is as low as~1.2, and value of k is particularly low, which suggests its potential application in antireflective devices. In addition, the intrinsic refractive index (n dense ) of the dense MOF materials evaluated according to their porosity increases with the number of the functional groups, and the n dense of the two nitro-substituted MOFs is greater than that of the single nitro-substituted one, and the latter is bigger than that of hydroxyl-substituted one, which is close to that of amino-functionalized one. The diversity of ligands in MOFs makes them a promising new generation of optical materials.
“…By comparison, given that Pd and Pt have nearly the same structures (the same group of the periodic table, the face-centered cubic (fcc) crystal structure and the similar lattice constants) [27,28], the PdPt bimetallic nanoparticles (NPs) are especially attractive for catalyzing multiple reactions due to the presence of the powerful catalytic components of Pd and Pt. Meanwhile, the incorporation of Pd into Pt-based bimetals can not only significantly reduce the cost of the catalysts by decreasing the amount of Pt, but also enhance the catalytic properties while reducing the CO poisoning effect due to a strong coupling between these two metals [8,29].…”
This paper demonstrates a one-pot approach to produce highly dispersed dendritic palladium-platinum bimetallic nanoparticles (NPs) with small particle size, tunable composition and high catalytic activity. Herein, the PdPt bimetallic NPs have been obtained using bayberry tannin (BT) as both the reducing agent and surfactant. Additionally, the PdPt bimetallic NPs with different Pd/Pt atomic ratios can be prepared by just varying the amounts of the Pd and Pt precursors. Most importantly, the as-prepared Pd 52 Pt 48 catalyst exhibits the optimal catalytic activities compared with the other compositional PdPt NPs (Pd 82 Pt 18 , Pd 69 Pt 31 , and Pd 36 Pt 64 ) and commercial Pt/C (20 wt.%) catalyst for the methanol oxidation reaction (MOR). Meanwhile, Pd 52 Pt 48 also shows better CO tolerance, which can be attributed to the unique dendritic structure and the synergistic effect between Pd and Pt. With evident advantages of the facile preparation and enhanced catalytic performance, it holds great promise as a high-performance catalyst for electrochemical energy conversion.
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