scholarly journals Tuning Mg(OH)2 Structural, Physical, and Morphological Characteristics for Its Optimal Behavior in a Thermochemical Heat-Storage Application

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1091
Author(s):  
Elpida Piperopoulos ◽  
Marianna Fazio ◽  
Emanuela Mastronardo ◽  
Maurizio Lanza ◽  
Candida Milone

Thermochemical materials (TCM) are among the most promising systems to store high energy density for long-term energy storage. To be eligible as candidates, the materials have to fit many criteria such as complete reversibility of the reaction and cycling stability, high availability of the material at low cost, environmentally friendliness, and non-toxicity. Among the most promising TCM, the Mg(OH)2/MgO system appears worthy of attention for its properties in line with those required. In the last few decades, research focused its attention on the optimization of attractive hydroxide performance to achieve a better thermochemical response, however, often negatively affecting its energy density per unit of volume and therefore compromising its applicability on an industrial scale. In this study, pure Mg(OH)2 was developed using different synthesis procedures. Reverse deposition precipitation and deposition precipitation methods were used to obtain the investigated samples. By adding a cationic surfactant (cetyl trimethylammonium bromide), deposition precipitation Mg(OH)2 (CTAB-DP-MH) or changing the precipitating precursor (N-DP-MH), the structural, physical and morphological characteristics were tuned, and the results were compared with a commercial Mg(OH)2 sample. We identified a correlation between the TCM properties and the thermochemical behavior. In such a context, it was demonstrated that both CTAB-DP-MH and N-DP-MH improved the thermochemical performances of the storage medium concerning conversion (64 wt.% and 74 wt.% respectively) and stored and released heat (887 and 1041 kJ/kgMg(OH)2). In particular, using the innovative technique not yet investigated for thermal energy storage (TES) materials, with NaOH as precipitating precursor, N-DP-MH reached the highest stored and released heat capacity per volume unit, ~684 MJ/m3.

2019 ◽  
Vol 12 (05) ◽  
pp. 1930004 ◽  
Author(s):  
Xin Cao ◽  
Huan Xia ◽  
Xiangyu Zhao

Alkaline zinc-based rechargeable batteries (AZRBs) are competitive candidates for future electrical energy storage because of their low-cost, eco-friendliness and high energy density. However, plagued by dendrites, the AZRBs suffer from drastic decay in electrochemical properties and safety. This review elucidates fundamentals of zinc dendritic formation and summarizes the strategies, including electrode design and modification, electrolyte optimization and separator improvement, for suppressing zinc dendritic growth.


2020 ◽  
Author(s):  
Jian Luo ◽  
Bo Hu ◽  
Wenda Wu ◽  
Maowei Hu ◽  
Leo Liu

Redox flow batteries (RFBs) have been recognized as a promising option for scalable and dispatchable renewable energy storage (e.g. solar and wind energy). Zinc metal represents a low cost, high capacity anode material to develop high energy density aqueous redox flow batteries. However, the energy storage applications of traditional inorganic Zn halide flow batteries are primarily plagued by the material challenges of traditional halide cathode electrolytes (e.g. bromine) including corrosion, toxicity, and severe crossover. As reported here, we have developed a bipolar Zinc-ferrocene salt compound, Zinc 1,1’-bis(3-sulfonatopropyl)ferrocene, Zn[Fc(SPr)2] (1.80 M solubility or 48.2 Ah/L charge storage capacity) – a robust, energy-dense, bipolar redox-active electrolyte material for high performance Zn organic RFBs. Using a low-cost porous Daramic membrane, the Zn[Fc(SPr)2] aqueous organic redox flow battery (AORFB) has worked in dual-flow and single-flow modes. It has manifested outstanding current, energy, and power performance, specifically, operating at high current densities of up to 200 mA/cm2 and delivering an energy efficiency of up to 81.5% and a power density of up to 270.5 mW/cm2. A Zn[Fc(SPr)2] AORFB demonstrated an energy density of 20.2 Wh/L and displayed 100% capacity retention for 2000 cycles (1284 hr or 53.5 days). The Zn[Fc(SPr)2] ionic bipolar electrolyte not only offers record-setting, highly-stable, energy-dense, and the most powerful Zn-organic AORFBs to date, but it also provides a new paradigm to develop even more advanced redox materials for scalable energy storage.


2017 ◽  
Vol 129 (47) ◽  
pp. 15149-15153 ◽  
Author(s):  
Congxin Xie ◽  
Yinqi Duan ◽  
Wenbin Xu ◽  
Huamin Zhang ◽  
Xianfeng Li

2015 ◽  
Vol 27 (39) ◽  
pp. 5915-5922 ◽  
Author(s):  
Xiaochuan Lu ◽  
Mark E. Bowden ◽  
Vincent L. Sprenkle ◽  
Jun Liu

Author(s):  
Lin Qiao ◽  
Congxin Xie ◽  
Mingjun Nan ◽  
Huamin Zhang ◽  
Xiangkun Ma ◽  
...  

Manganese-based flow batteries have attracted increasing interest due to their advantage of low cost and high energy density. However, the sediment (MnO2) from Mn3+ disproportionation reaction creates the risk to...


2017 ◽  
Vol 5 (41) ◽  
pp. 21898-21902 ◽  
Author(s):  
M. Freire ◽  
O. I. Lebedev ◽  
A. Maignan ◽  
C. Jordy ◽  
V. Pralong

Nowadays the energy storage challenge is to develop a low cost, ecofriendly, high energy density material, showing a reversible capacity higher than 250 mA h g−1.


MRS Advances ◽  
2019 ◽  
Vol 4 (15) ◽  
pp. 857-863 ◽  
Author(s):  
Qiang Wu ◽  
Jim P. Zheng ◽  
Mary Hendrickson ◽  
Edward J. Plichta

AbstractWe report a roll-to-roll dry processing for making low cost and high performance electrodes for lithium-ion batteries (LIBs). Currently, the electrodes for LIBs are made with a slurry casting procedure (wet method). The dry electrode fabrication is a three-step process including: step 1 of uniformly mixing electrode materials powders comprising an active material, a carbonaceous conductor and the soft polymer binder; step 2 of forming a free-standing, continuous electrode film by pressing the mixed powders together through the gap between two rolls of a roll-mill; and step 3 of roll-to-roll laminating the electrode film onto a substrate such as a current collector. Compared with the conventional wet slurry electrode manufacturing method, the dry manufactural procedure and infrastructure are simpler, the production cost is lower, and the process eliminates volatile organic compound emission and is more environmentally friendly, and the ability of making thick (>120µm) electrodes with high tap density results in high energy density of final energy storage device. A prototype LIBs of LiNi0.6Mn0.2Co0.2O2 (NMC622)/graphite also has 230 Wh/ kg energy density.


2021 ◽  
Author(s):  
Xiao Tang ◽  
Dong Zhou ◽  
Bao Zhang ◽  
Shijian Wang ◽  
Peng Li ◽  
...  

Abstract Non–aqueous rechargeable multivalent metal (Ca, Mg, Al, etc.) batteries are promising for large–scale energy storage due to their low cost. However, their practical applications face formidable challenges owing to low electrochemical reversibility and dendrite growth of multivalent metal anodes, sluggish kinetics of multivalent ion in metal oxide cathodes, and poor electrode compatibility of flammable organic electrolytes. To overcome these intrinsic hurdles, we develop aqueous multivalent ion batteries to replace the prevailing non–aqueous multivalent metal batteries by using wide–window super–concentrated aqueous gel electrolytes, the versatile high–capacity sulfur anodes, and high–voltage metal oxide cathodes. This rationally designed aqueous battery chemistry enables the long–lasting multivalent ion batteries featured with increased high energy density, reversibility and safety. As a demonstration model, a calcium ion−sulfur||metal oxide full cell exhibited a high energy density of 110 Wh kg–1 with outstanding cycling stability. Molecular dynamics modelling and experimental investigations revealed that the side reactions could be significantly restrained through the suppressed water activity and formation of protective inorganic solid electrolyte interphase in the aqueous gel electrolyte. The unique redox chemistry has also been successfully extended to aqueous magnesium ion and aluminum ion−sulfur||metal oxide batteries. This work will boost aqueous multivalent ion batteries for low−cost large–scale energy storage.


Author(s):  
Salunkhe Tejaswi Tanaji ◽  
Abhijit N Kadam ◽  
Weldejewergis Gebrewahid Kidanu ◽  
Sang-Wha Lee ◽  
Tuan Loi Nguyen ◽  
...  

Lithium dual-ion batteries (LDIBs) are currently receiving great attention as energy-storage systems due to their low cost, environmentally friendly characteristics, and good safety features. Herein, mesoporous Co3Sn2 and SnO2 core-shell...


2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Jingdong Huang ◽  
Jing Zeng ◽  
Kunjie Zhu ◽  
Ruizhi Zhang ◽  
Jun Liu

AbstractThere is an urgent need for low-cost, high-energy-density, environmentally friendly energy storage devices to fulfill the rapidly increasing need for electrical energy storage. Multi-electron redox is considerably crucial for the development of high-energy-density cathodes. Here we present high-performance aqueous zinc–manganese batteries with reversible Mn2+/Mn4+ double redox. The active Mn4+ is generated in situ from the Mn2+-containing MnOx nanoparticles and electrolyte. Benefitting from the low crystallinity of the birnessite-type MnO2 as well as the electrolyte with Mn2+ additive, the MnOx cathode achieves an ultrahigh energy density with a peak of 845.1 Wh kg−1 and an ultralong lifespan of 1500 cycles. The combination of electrochemical measurements and material characterization reveals the reversible Mn2+/Mn4+ double redox (birnessite-type MnO2 ↔ monoclinic MnOOH and spinel ZnMn2O4 ↔ Mn2+ ions). The reversible Mn2+/Mn4+ double redox electrode reaction mechanism offers new opportunities for the design of low-cost, high-energy-density cathodes for advanced rechargeable aqueous batteries.


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