scholarly journals Requirements for Beneficial Electrochemical Restructuring: A Model Study on a Cobalt Oxide in Selected Electrolytes

Author(s):  
Javier Villalobos ◽  
Diego Gonzales-Flores ◽  
Roberto Urcuyo ◽  
Mavis L. Montero ◽  
Götz Schuck ◽  
...  

<p>The requirements for beneficial materials restructuring into a higher performance OER electrocatalyst are still a largely open question. Here we use Erythrite (Co<sub>3</sub>(AsO<sub>4</sub>)<sub>2 </sub>8H<sub>2</sub>O) as a Co-based OER electrocatalyst to evaluate its catalytic properties during in-situ restructuring into an amorphous Co-based catalyst in four different electrolytes at pH 7. Using diffraction, microscopy and spectroscopy, we observed a strong effect in the restructuring kinetics depending of the anions in the electrolyte. Only carbonate electrolyte could activate the catalyst electrode, which we relate to its slow restructuring kinetics. While its turnover frequency (TOF) reduced from 2.84 O<sub>2 </sub>Co<sup>-1 </sup>s<sup>-1</sup> to a constant value of 0.10 O<sub>2</sub> Co<sup>-1 </sup>s<sup>-1</sup> after ~ 300 cycles, the number of redox active sites continuously increased, which explained the current increase of around 100%. The final activated material owns an adequate local order, a high Co oxidation state and a high number of redox-active Co ions, which we identify as the trinity for enhancing the OER activity. Thus, this work provides new insights into for the rational design of high-performance OER catalysts by electrochemical restructuring.</p>

2021 ◽  
Author(s):  
Javier Villalobos ◽  
Diego Gonzales-Flores ◽  
Roberto Urcuyo ◽  
Mavis L. Montero ◽  
Götz Schuck ◽  
...  

<p>The requirements for beneficial materials restructuring into a higher performance OER electrocatalyst are still a largely open question. Here we use Erythrite (Co<sub>3</sub>(AsO<sub>4</sub>)<sub>2 </sub>8H<sub>2</sub>O) as a Co-based OER electrocatalyst to evaluate its catalytic properties during in-situ restructuring into an amorphous Co-based catalyst in four different electrolytes at pH 7. Using diffraction, microscopy and spectroscopy, we observed a strong effect in the restructuring kinetics depending of the anions in the electrolyte. Only carbonate electrolyte could activate the catalyst electrode, which we relate to its slow restructuring kinetics. While its turnover frequency (TOF) reduced from 2.84 O<sub>2 </sub>Co<sup>-1 </sup>s<sup>-1</sup> to a constant value of 0.10 O<sub>2</sub> Co<sup>-1 </sup>s<sup>-1</sup> after ~ 300 cycles, the number of redox active sites continuously increased, which explained the current increase of around 100%. The final activated material owns an adequate local order, a high Co oxidation state and a high number of redox-active Co ions, which we identify as the trinity for enhancing the OER activity. Thus, this work provides new insights into for the rational design of high-performance OER catalysts by electrochemical restructuring.</p>


2021 ◽  
Author(s):  
Javier Villalobos ◽  
Diego Gonzales-Flores ◽  
Roberto Urcuyo ◽  
Mavis L. Montero ◽  
Götz Schuck ◽  
...  

<p>The requirements for beneficial materials restructuring into a higher performance OER electrocatalyst are still a largely open question. Here we use Erythrite (Co<sub>3</sub>(AsO<sub>4</sub>)<sub>2 </sub>8H<sub>2</sub>O) as a Co-based OER electrocatalyst to evaluate its catalytic properties during in-situ restructuring into an amorphous Co-based catalyst in four different electrolytes at pH 7. Using diffraction, microscopy and spectroscopy, we observed a strong effect in the restructuring kinetics depending of the anions in the electrolyte. Only carbonate electrolyte could activate the catalyst electrode, which we relate to its slow restructuring kinetics. While its turnover frequency (TOF) reduced from 2.84 O<sub>2 </sub>Co<sup>-1 </sup>s<sup>-1</sup> to a constant value of 0.10 O<sub>2</sub> Co<sup>-1 </sup>s<sup>-1</sup> after ~ 300 cycles, the number of redox active sites continuously increased, which explained the current increase of around 100%. The final activated material owns an adequate local order, a high Co oxidation state and a high number of redox-active Co ions, which we identify as the trinity for enhancing the OER activity. Thus, this work provides new insights into for the rational design of high-performance OER catalysts by electrochemical restructuring.</p>


2020 ◽  
Vol 8 (44) ◽  
pp. 23436-23454
Author(s):  
Ahmed Al-Shahat Eissa ◽  
Nam Hoon Kim ◽  
Joong Hee Lee

A high-performance and sustainable electrocatalyst for the oxygen reduction reaction is fabricated by a single-step doping/annealing strategy.


Author(s):  
Xiubei Yang ◽  
Chao Lin ◽  
Diandian Han ◽  
Gaojie Li ◽  
Chao Huang ◽  
...  

Covalent organic frameworks (COFs) with reversible redox-active sites showed great potential application in constructing electrode materials of lithium-ion batteries (LIBs), whereas their further application is largely restricted by the poor...


Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 459 ◽  
Author(s):  
Heng Luo ◽  
Hang Lei ◽  
Yufei Yuan ◽  
Yongyin Liang ◽  
Yi Qiu ◽  
...  

The rational design and development of the low-cost and effective electrocatalysts toward oxygen evolution reaction (OER) are essential in the storage and conversion of clean and renewable energy sources. Herein, a ternary copper-cobalt sulfide nanosheets electrocatalysts (denoted as CuCoS/CC) for electrochemical water oxidation has been synthesized on carbon cloth (CC) via the sulfuration of CuCo-based precursors. The obtained CuCoS/CC reveals excellent electrocatalytic performance toward OER in 1.0 M KOH. It exhibits a particularly low overpotential of 276 mV at current density of 10 mA cm−2, and a small Tafel slope (58 mV decade−1), which is superior to the current commercialized noble-metal electrocatalysts, such as IrO2. Benefiting from the synergistic effect of Cu and Co atoms and sulfidation, electrons transport and ions diffusion are significantly enhanced with the increase of active sites, thus the kinetic process of OER reaction is boosted. Our studies will serve as guidelines in the innovative design of non-noble metal electrocatalysts and their application in electrochemical water splitting


2021 ◽  
Author(s):  
Xiaoming He ◽  
Xiujuan Wang ◽  
Wenhao Xue ◽  
Guangyuan Gao ◽  
Ling Chen ◽  
...  

Development of novel organics that exhibit multiple and stable redox states, limited solubility and improved conductivity is a highly rewarding direction for improving the performance of lithium-ion batteries (LIBs). As biologically derived organic molecules, carbonylpyridinium compounds have desirable and tunable redox properties, making them suitable candidates for battery applications. In this work, we report a structural evolution of carbonylpyridinium-based redox-active organics, from 2-electron accepting BMP to 4-electron accepting small, conjugated molecules (1, 2), and then to the corresponding conjugated polymers (CP1, CP2). Through suppression of dissolution and increasing electrochemical conductivity, the LIBs performance can be gradually enhanced. At a relatively high current of 0.5 A g-1, high specific capacities for 1 (100 mAh g-1), 2 (260 mAh g-1), CP1 (360 mAh g-1) and CP2 (540 mAh g-1) can be reached after 240 cycles. Particularly, the rate performance and cycling stability of CP2 surpasses many reported commercial inorganic and organic electrode materials. This work provides a promising new carbonylpyridinium-based building block featured with multiple redox centers, on the way to high performance Li-organic batteries.


2021 ◽  
Author(s):  
Zifeng Tian ◽  
hongyan zeng ◽  
Shi-Bing Lv ◽  
YiWen Long ◽  
Sheng Xu ◽  
...  

Abstract A facile two-step hydrothermal approach with post-sulfurization treatment was put forward to construct the mixed transition metal sulfide (NiCoZnS) with a high electrochemical performance. The different morphologies of NiCoZnS materials were successfully fabricated by adjusted the Ni/Co molar ratio of the NiCoZn(OH)F precursor. Moreover, the in-situ phase transformation from the NiCoZn(OH)F phase to Zn0.76Co0.24S and NiCo2S4 phases and lattice defects via the S2− ion-exchange were determined by XRD, TEM and XPS techniques, which improved electric conductivity and interfacial active sites of the NiCoZnS, and so promoted the reaction kinetics. Significantly, the urchin-like NiCoZnS1/1 prepared at the Ni/Co molar ratio of 1.0 exhibited promising electrochemical performances with high capacitance and excellent cycling stability. Furthermore, the asymmetric device (NiCoZnS//AC) using NiCoZnS1/1 as the positive electrode had excellent supercapacitor performances with an energy density of 57.8 Wh·kg–1 at a power density of 750 W·kg–1 as well as a long cycle life (79.2% capacity retention after 10000 cycles), indicating the potential application in high-performance supercapacitors.


2019 ◽  
Vol 7 (42) ◽  
pp. 24462-24476 ◽  
Author(s):  
Thangasamy Deepalakshmi ◽  
Thanh Tuan Nguyen ◽  
Nam Hoon Kim ◽  
Kil To Chong ◽  
Joong Hee Lee

A novel strategy is proposed to design and fabrication of hierarchical tin nickel selenide nanosheets with highly exposed active sites for flexible and wearable energy storage systems.


2020 ◽  
Vol 4 (4) ◽  
pp. 1863-1874 ◽  
Author(s):  
Bezawit Z. Desalegn ◽  
Harsharaj S. Jadhav ◽  
Jeong Gil Seo

Heterostructuring assisted trimetallic transition metal phoshide with in situ generated active sites, exhibits superior catalytic activity towards oxygen evolution reaction in alkaline medium.


2021 ◽  
Author(s):  
M Sangeethavidhya ◽  
Rathinam Yuvakkumar ◽  
Ganesan Ravi ◽  
Saravanakumar Balasubramaniam ◽  
Dhayalan Velauthapillai

Approaching into the part of redox active sites in charge/discharge material is extremely noteworthy for the progress of high performance of the polyhedron structured NiSe2@MoSe2 (NMS hydrolysed for 18h) as...


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