Low Potential Prussian Blue Analogs: Manganese Hexacyanochromate

2019 ◽  
Author(s):  
Samuel Wheeler ◽  
Isaac Capone ◽  
Sarah Day ◽  
Chiu C. Tang ◽  
Mauro Pasta

Prussian blue analogues (PBAs) have recently shown outstanding electrochemical properties ascribable to their unique open-framework crystal structure that allows the reversible insertion of alkali ions with negligible perturbation to the framework itself. Many hexacyanoferrate materials have shown excellent properties and are some of the most promising sodium- and potassium-ion cathode materials in both aqueous and organic electrolytes. However, there is a distinct lack of candidate PBA materials that operate at low potentials as their characteristic crystalline framework shows instability. In this article we characterise the structure and electrochemical behavior of manganese hexacyanochromate which exhibits reversible sodium insertion at - 0.86 V vs. SHE (1.84 V vs. Na<sup>+</sup>/Na), whilst maintaining the characteristic PBA cubic structure. This is the lowest redox potential of reported PBA materials and shows fast kinetics in a high voltage water-in-salt electrolyte. Further reduction in potential in an organic electrolyte shows decomposition of the crystalline structure.

2019 ◽  
Author(s):  
Samuel Wheeler ◽  
Isaac Capone ◽  
Sarah Day ◽  
Chiu C. Tang ◽  
Mauro Pasta

Prussian blue analogues (PBAs) have recently shown outstanding electrochemical properties ascribable to their unique open-framework crystal structure that allows the reversible insertion of alkali ions with negligible perturbation to the framework itself. Many hexacyanoferrate materials have shown excellent properties and are some of the most promising sodium- and potassium-ion cathode materials in both aqueous and organic electrolytes. However, there is a distinct lack of candidate PBA materials that operate at low potentials as their characteristic crystalline framework shows instability. In this article we characterise the structure and electrochemical behavior of manganese hexacyanochromate which exhibits reversible sodium insertion at - 0.86 V vs. SHE (1.84 V vs. Na<sup>+</sup>/Na), whilst maintaining the characteristic PBA cubic structure. This is the lowest redox potential of reported PBA materials and shows fast kinetics in a high voltage water-in-salt electrolyte. Further reduction in potential in an organic electrolyte shows decomposition of the crystalline structure.


Biosensors ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 193
Author(s):  
Galina Z. Gayda ◽  
Olha M. Demkiv ◽  
Yanna Gurianov ◽  
Roman Ya. Serkiz ◽  
Halyna M. Klepach ◽  
...  

Prussian blue analogs (PBAs) are well-known artificial enzymes with peroxidase (PO)-like activity. PBAs have a high potential for applications in scientific investigations, industry, ecology and medicine. Being stable and both catalytically and electrochemically active, PBAs are promising in the construction of biosensors and biofuel cells. The “green” synthesis of PO-like PBAs using oxido-reductase flavocytochrome b2 is described in this study. When immobilized on graphite electrodes (GEs), the obtained green-synthesized PBAs or hexacyanoferrates (gHCFs) of transition and noble metals produced amperometric signals in response to H2O2. HCFs of copper, iron, palladium and other metals were synthesized and characterized by structure, size, catalytic properties and electro-mediator activities. The gCuHCF, as the most effective PO mimetic with a flower-like micro/nano superstructure, was used as an H2O2-sensitive platform for the development of a glucose oxidase (GO)-based biosensor. The GO/gCuHCF/GE biosensor exhibited high sensitivity (710 A M−1m−2), a broad linear range and good selectivity when tested on real samples of fruit juices. We propose that the gCuHCF and other gHCFs synthesized via enzymes may be used as artificial POs in amperometric oxidase-based (bio)sensors.


2016 ◽  
Vol 18 (4) ◽  
pp. 3188-3196 ◽  
Author(s):  
D. Dedovets ◽  
P. Bauduin ◽  
J. Causse ◽  
L. Girard ◽  
O. Diat

We showed fully reversible, ionic strength controlled self-assembly of Prussian blue analogues nano-tiles into large superlattice structures.


2016 ◽  
Vol 4 (11) ◽  
pp. 4211-4223 ◽  
Author(s):  
Mauro Pasta ◽  
Richard Y. Wang ◽  
Riccardo Ruffo ◽  
Ruimin Qiao ◽  
Hyun-Wook Lee ◽  
...  

The interplay between electrochemical properties, crystal structure, and chemical bonding of Prussian Blue analogues determines their suitability for grid-scale aqueous batteries.


Crystals ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 112 ◽  
Author(s):  
Maria Zentkova ◽  
Marian Mihalik

We present the review of pressure effect on the crystal structure and magnetic properties of Cr(CN)6-based Prussian blue analogues (PBs). The lattice volume of the fcc crystal structure space group Fm 3 ¯ m in the Mn-Cr-CN-PBs linearly decreases for p ≤ 1.7 GPa, the change of lattice size levels off at 3.2 GPa, and above 4.2 GPa an amorphous-like structure appears. The crystal structure recovers after removal of pressure as high as 4.5 GPa. The effect of pressure on magnetic properties follows the non-monotonous pressure dependence of the crystal lattice. The amorphous like structure is accompanied with reduction of the Curie temperature (TC) to zero and a corresponding collapse of the ferrimagnetic moment at 10 GPa. The cell volume of Ni-Cr-CN-PBs decreases linearly and is isotropic in the range of 0–3.1 GPa. The Raman spectra can indicate a weak linkage isomerisation induced by pressure. The Curie temperature in Mn2+-CrIII-PBs and Cr2+-CrIII-PBs with dominant antiferromagnetic super-exchange interaction increases with pressure in comparison with decrease of TC in Ni2+-CrIII-PBs and Co2+-CrIII-PBs ferromagnets. TC increases with increasing pressure for ferrimagnetic systems due to the strengthening of magnetic interaction because pressure, which enlarges the monoelectronic overlap integral S and energy gap ∆ between the mixed molecular orbitals. The reduction of bonding angles between magnetic ions connected by the CN group leads to a small decrease of magnetic coupling. Such a reduction can be expected on both compounds with ferromagnetic and ferrimagnetic ordering. In the second case this effect is masked by the increase of coupling caused by the enlarged overlap between magnetic orbitals. In the case of mixed ferro–ferromagnetic systems, pressure affects μ(T) by a different method in Mn2+–N≡C–CrIII subsystem and CrIII–C≡N–Ni2+ subsystem, and as a consequence Tcomp decreases when the pressure is applied. The pressure changes magnetization processes in both systems, but we expect that spontaneous magnetization is not affected in Mn2+-CrIII-PBs, Ni2+-CrIII-PBs, and Co2+-CrIII-PBs. Pressure-induced magnetic hardening is attributed to a change in magneto-crystalline anisotropy induced by pressure. The applied pressure reduces saturated magnetization of Cr2+-CrIII-PBs. The applied pressure p = 0.84 GPa induces high spin–low spin transition of cca 4.5% of high spin Cr2+. The pressure effect on magnetic properties of PBs nano powders and core–shell heterostructures follows tendencies known from bulk parent PBs.


2021 ◽  
Author(s):  
Xijun Wei ◽  
Yingze Song ◽  
Donghai Wu ◽  
Xu Dong Liu ◽  
Houyang Chen ◽  
...  

Prussian blue analogs (PBAs) as a type of emerging metal-organic frameworks (MOFs) show great potential in the realm of aqueous potassium-ion batteries (AKIBs) owing to their open-framework structure, 3D channels...


2015 ◽  
Vol 71 (4) ◽  
pp. 330-337 ◽  
Author(s):  
Sabina Kovač ◽  
Ljiljana Karanović ◽  
Tamara Đorđević

Two isostructural diarsenates, SrZnAs2O7(strontium zinc diarsenate), (I), and BaCuAs2O7[barium copper(II) diarsenate], (II), have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The three-dimensional open-framework crystal structure consists of corner-sharingM2O5(M2 = Zn or Cu) square pyramids and diarsenate (As2O7) groups. Each As2O7group shares its five corners with five differentM2O5square pyramids. The resulting framework delimits two types of tunnels aligned parallel to the [010] and [100] directions where the large divalent nine-coordinatedM1 (M1 = Sr or Ba) cations are located. The geometrical characteristics of theM1O9,M2O5and As2O7groups of known isostructural diarsenates, adopting the general formulaM1IIM2IIAs2O7(M1II= Sr, Ba, Pb;M2II= Mg, Co, Cu, Zn) and crystallizing in the space groupP21/n, are presented and discussed.


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