scholarly journals In situ healing of dendrites in a potassium metal battery

2020 ◽  
Vol 117 (11) ◽  
pp. 5588-5594 ◽  
Author(s):  
Prateek Hundekar ◽  
Swastik Basu ◽  
Xiulin Fan ◽  
Lu Li ◽  
Anthony Yoshimura ◽  
...  

The use of potassium (K) metal anodes could result in high-performance K-ion batteries that offer a sustainable and low-cost alternative to lithium (Li)-ion technology. However, formation of dendrites on such K-metal surfaces is inevitable, which prevents their utilization. Here, we report that K dendrites can be healed in situ in a K-metal battery. The healing is triggered by current-controlled, self-heating at the electrolyte/dendrite interface, which causes migration of surface atoms away from the dendrite tips, thereby smoothening the dendritic surface. We discover that this process is strikingly more efficient for K as compared to Li metal. We show that the reason for this is the far greater mobility of surface atoms in K relative to Li metal, which enables dendrite healing to take place at an order-of-magnitude lower current density. We demonstrate that the K-metal anode can be coupled with a potassium cobalt oxide cathode to achieve dendrite healing in a practical full-cell device.

Author(s):  
Kathryn Holguin ◽  
Motahareh Mohammadiroudbari ◽  
Kaiqiang Qin ◽  
Chao Luo

Na-ion batteries (NIBs) are promising alternatives to Li-ion batteries (LIBs) due to the low cost, abundance, and high sustainability of sodium resources. However, the high performance of inorganic electrode materials...


2021 ◽  
Vol MA2021-02 (3) ◽  
pp. 407-407
Author(s):  
Gustavo Ramirez ◽  
Anna Halajko ◽  
Glenn G. Amatucci

Author(s):  
Xiaojuan Shen ◽  
Xuan Zhang ◽  
Tongfei Wang ◽  
Songjun Li ◽  
Zhaoqiang Li

In this study, a novel 3D porous Si-based supercapacitor electrode was developed by the simple solution method, which involved firstly the in-situ polymerization of polyaniline particles (PANI) on the Si...


2021 ◽  
Author(s):  
Xianzhong Yang ◽  
Chao Li ◽  
Zhongti Sun ◽  
Shuai Yang ◽  
Zixiong Shi ◽  
...  

Abstract Zn metal anode has garnered growing scientific and industrial interest owing to its appropriate redox potential, low cost and good safety. Nevertheless, the instability of Zn metal, caused by dendrite formation, hydrogen evolution and side reactions, gives rise to poor electrochemical stability and unsatisfactory cycling life, greatly hampering large-scale utilization. Herein, an in-situ grown ZnSe layer with controllable thickness is crafted over one side of commercial Zn foil via chemical vapor deposition, aiming to achieve optimized interfacial manipulation between aqueous electrolyte/Zn anode. Thus-derived ZnSe overlayer not only prevents water penetration and restricts Zn2+ two-dimensional diffusion, but also homogenizes the electric field at the interface and facilitates favorable (002) plane growth of Zn. As a result, dendrite-free and homogeneous Zn deposition is obtained; side reactions are concurrently inhibited. In consequence, a high Coulombic efficiency of 99.2% and high cyclic stability for 860 cycles at 1.0 mA cm–2 in symmetrical cells is harvested. Meanwhile, when paired with V2O5 cathode, assembled full cell achieves an outstanding initial capacity (200 mAh g–1) and elongated lifespan (a capacity retention of 84% after 1000 cycles) at 5.0 A g–1. Our highly reversible Zn anode enabled by the interfacial manipulation strategy is anticipated to satisfy the demand of industrial and commercial use.


Author(s):  
Jiawei Wu ◽  
Jing Chen ◽  
Xiaodong Wang ◽  
An'an Zhou ◽  
Zhenglong Yang

For the higher safety and energy density, solid-state electrolyte with better mechanical strength, thermal and electrochemical stability is a perfect choice. To improve the performance of PEO, usage of low-cost...


Nanoscale ◽  
2019 ◽  
Vol 11 (35) ◽  
pp. 16621-16634 ◽  
Author(s):  
Ghasem Barati Darband ◽  
Mahmood Aliofkhazraei ◽  
Suyeon Hyun ◽  
Alireza Sabour Rouhaghdam ◽  
Sangaraju Shanmugam

Ni–Co–Fe mixed sulfide ultrathin nanosheets obtained by electrodeposition method exhibits excellent electrocatalytic activity. The Ni–Co–Fe nanosheets require the overpotential of 106 and 207 mV to generate 10 mA cm−2 current density for the HER, and OER, respectively.


Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 926 ◽  
Author(s):  
Yury Kutin ◽  
Nicholas Cox ◽  
Wolfgang Lubitz ◽  
Alexander Schnegg ◽  
Olaf Rüdiger

Here we report an in situ electron paramagnetic resonance (EPR) study of a low-cost, high-stability cobalt oxide electrodeposited material (Co-Pi) that oxidizes water at neutral pH and low over-potential, representing a promising system for future large-scale water splitting applications. Using CW X-band EPR we can follow the film formation from a Co(NO3)2 solution in phosphate buffer and quantify Co uptake into the catalytic film. As deposited, the film shows predominantly a Co(II) EPR signal, which converts into a Co(IV) signal as the electrode potential is increased. A purpose-built spectroelectrochemical cell allowed us to quantify the extent of Co(II) to Co(IV) conversion as a function of potential bias under operating conditions. Consistent with its role as an intermediate, Co(IV) is formed at potentials commensurate with electrocatalytic O2 evolution (+1.2 V, vs. SHE). The EPR resonance position of the Co(IV) species shifts to higher fields as the potential is increased above 1.2 V. Such a shift of the Co(IV) signal may be assigned to changes in the local Co structure, displaying a more distorted ligand field or more ligand radical character, suggesting it is this subset of sites that represents the catalytically ‘active’ component. The described spectroelectrochemical approach provides new information on catalyst function and reaction pathways of water oxidation.


2019 ◽  
Vol 10 ◽  
pp. 281-293 ◽  
Author(s):  
Donghui Zheng ◽  
Man Li ◽  
Yongyan Li ◽  
Chunling Qin ◽  
Yichao Wang ◽  
...  

Developing a facile and environmentally friendly approach to the synthesis of nanostructured Ni(OH)2 electrodes for high-performance supercapacitor applications is a great challenge. In this work, we report an extremely simple route to prepare a Ni(OH)2 nanopetals network by immersing Ni nanofoam in water. A binder-free composite electrode, consisting of Ni(OH)2 nanopetals network, Ni nanofoam interlayer and Ni-based metallic glass matrix (Ni(OH)2/Ni-NF/MG) with sandwich structure and good flexibility, was designed and finally achieved. Microstructure and morphology of the Ni(OH)2 nanopetals were characterized. It is found that the Ni(OH)2 nanopetals interweave with each other and grow vertically on the surface of Ni nanofoam to form an “ion reservoir”, which facilitates the ion diffusion in the electrode reaction. Electrochemical measurements show that the Ni(OH)2/Ni-NF/MG electrode, after immersion in water for seven days, reveals a high volumetric capacitance of 966.4 F/cm3 at a current density of 0.5 A/cm3. The electrode immersed for five days exhibits an excellent cycling stability (83.7% of the initial capacity after 3000 cycles at a current density of 1 A/cm3). Furthermore, symmetric supercapacitor (SC) devices were assembled using ribbons immersed for seven days and showed a maximum volumetric energy density of ca. 32.7 mWh/cm3 at a power density of 0.8 W/cm3, and of 13.7 mWh/cm3 when the power density was increased to 2 W/cm3. The fully charged SC devices could light up a red LED. The work provides a new idea for the synthesis of nanostructured Ni(OH)2 by a simple approach and ultra-low cost, which largely extends the prospect of commercial application in flexible or wearable devices.


2016 ◽  
Vol 40 (8) ◽  
pp. 6881-6889 ◽  
Author(s):  
Cuiping Yu ◽  
Yan Wang ◽  
Jianfang Zhang ◽  
Xia Shu ◽  
Jiewu Cui ◽  
...  

Novel nanocomposite NiCo2O4/C-TNAs were synthesized for high-performance supercapacitors with a specific capacitance of 934.9 F g−1 at a current density of 2 A g−1.


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