Abstract:Layered
double hydroxides (LDHs) are attracting intense research interests
as methyl orange (MO) adsorbent due to the unique anionic exchange
ability. Herein, ultrasmall NiAl LDHs with Cl– intercalation
were prepared by a facile method combining hydrothermal method with
acid salt treatment. As a result, the as-prepared NiAl LDHs displayed
favorable removal performance toward MO from aqueous solution due
to the negligible carbonate contamination and ultrasmall nanosheets
(about 50 nm). The maximum experimental … Show more
“…However, from the perspective of intercalation thermodynamics, the high affinity between CO 3 2− and the host layer of LDHs has a negative effect on the intercalation of OH − . [ 60 ] Hence, we hope to obtain LDHs with the intercalation of other anions by simple and operable methods and then enhance the interaction between the LDHs and the OH − . Some other anions such as OH − , NO 3 − , SO 4 2− , and Cl − are promising candidate anions and have been widely researched.…”
and Technology (HKUST). He is now a professor of the College of Civil and Transportation Engineering of Shenzhen University. His research interests include structure and corrosion inhibition materials of coastal concrete and their durability evaluation.
“…However, from the perspective of intercalation thermodynamics, the high affinity between CO 3 2− and the host layer of LDHs has a negative effect on the intercalation of OH − . [ 60 ] Hence, we hope to obtain LDHs with the intercalation of other anions by simple and operable methods and then enhance the interaction between the LDHs and the OH − . Some other anions such as OH − , NO 3 − , SO 4 2− , and Cl − are promising candidate anions and have been widely researched.…”
and Technology (HKUST). He is now a professor of the College of Civil and Transportation Engineering of Shenzhen University. His research interests include structure and corrosion inhibition materials of coastal concrete and their durability evaluation.
“…In the Ni 2p spectrum of Fe‐o‐NiAlOH, the binding energies (BEs) at 856.0 eV and 857.1 eV put down to Ni 2p 3/2 of Ni 2+ and Ni 3+ , respectively, and the high BEs at 873.7 eV and 874.7 eV put down to Ni 2p 1/2 of Ni 2+ and Ni 3+ , respectively, implying the coexistence of Ni 2+ and Ni 3+ in Fe‐o‐NiAlOH (Figure 3b) [40,48,49] . The Al 2p spectrum of Fe‐o‐NiAlOH (Figure 3c) exhibits a typical peak at 74.1 eV, confirming the trivalent oxidation state of Al in Fe‐o‐NiAlOH [50] . Ni 3p at 67.9 eV is also visible in the Al region (Figure 3c) [51–53] .…”
Interfacial structure engineering with multiple high‐oxidation‐state cations, especially those that show unstable higher‐valence during catalysis towards superior electron synergy, for high‐performance electrocatalysis is of great interest and full of challenges. Lattice distortion from lattice strain at phase boundaries as a result of interfacial structure engineering is also appealing. Fe oxyhydroxide containing Fe3+ lead to unstable Fe4+ with a short lifetime on edge/defect sites during steady‐state water‐oxidation catalysis. Such material was deliberately installed to achieve atom‐scale combination with Ni3+ relevant layered double hydroxide to construct high‐energy interfaces for high‐oxidation‐state cations synergy and induce lattice distortion. The Fe‐o‐NiAlOH exhibited prominent property toward oxygen evolution reaction with 202 mV to drive 10 mA cm−2. Fe‐o‐NiAlOH also showed hydrogen evolution reaction activity, requiring an overpotential of 180 mV for 10 mA cm−2. Alkaline water electrolyzer with Fe‐o‐NiAlOH as both anodic and cathodic electrodes required only 1.64 V to reach 10 mA cm−2. This work offers an effective well‐defined electrocatalyst and shows the synergetic protocol of unstable high‐oxidation‐state cations and lattice defects for high‐performance water decomposition catalysis.
“…The effect of the Cl – ion intercalation method on the adsorption capacity was investigated. Conventionally, Cl – ion intercalation has been successfully achieved by using a mixture with a high concentration of NaCl (4.00 M) and HCl (0.033 M). − The fabrication protocols are described in the Supporting Information. In our case, the facile procedure was introduced by using only HCl (0.33 M).…”
Section: Resultsmentioning
confidence: 99%
“…Most synthesized LDH adsorbents contain carbonate (CO 3 2– ) ions in the interlayer because they can easily capture carbon dioxide gas from the environment during preparation. It is difficult to achieve anion exchangeability because of the strong affinity between CO 3 2– ions and the metal host layer, resulting in a low adsorption capacity. , Consequently, an effective technique for preparing LDH adsorbents and modifying the interlayer is required to enhance the adsorption performance.…”
Layered
double hydroxides (LDHs) have attracted significant attention
as adsorbents for the removal of anions from wastewater. However,
it is challenging to develop a simple, economical, and environmentally
friendly method for fabricating efficient LDH adsorbents. In this
paper, we present an alternative approach for preparing a superb NiFe
LDH adsorbent via a single-step topochemical synthesis method based
on density functional theory (DFT) calculation. The NiFe LDH adsorbent
[Ni0.75Fe0.25(OH)2]·(CO3)0.125·0.25H2O was obtained via
the topotactic transformation of an oxide precursor (NaNi0.75Fe0.25O2), which was prepared by utilizing
the high-temperature flux method, in ultrapure water. When the oxide
precursor was soaked in ultrapure water, the host layer valence state
changed from Ni3+ and Fe3+ to Ni2+ and Fe3+, and carbonate (CO3
2–) ions were simultaneously intercalated in the interlayer. Thereafter,
the CO3
2– ions were deintercalated by
Cl– ions to increase the adsorption capacity. The
adsorbent exhibited high crystallinity, cation state, and porosity,
and unique particle shape. In addition, it showed superior adsorption
capacities of approximately 194.92, 176.15, and 146.28 mg g–1 toward phosphate, fluoride, and nitrate ions, respectively. The
adsorption capacity toward all the anions reached over 70% within
10 min. The adsorption behavior was investigated by performing from
adsorption kinetics, isotherm, and thermodynamics studies. The results
showed that the anions were endothermically and spontaneously chemisorbed
through an ion exchange process onto the adsorbent in a monolayer.
In addition, the as-prepared NiFe LDH adsorbent showed high stability
after multicycle testing.
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