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Ni3(NO3)2(OH)4
Nanoscale · 2024 ·Vol. 16 ·期 36 ·16933-16941 · IF 5.8

Yttrium doping stabilizes the structure of Ni3(NO3)2(OH)4 cathodes for application in advanced Ni–Zn batteries

Xinyu Feng,Siwen Zhang,Jiazhuo Li,Yingfang Hu,Rongyuan Ge,Yaowen Shi,Yali Yao,Bosi Yin,Tianyi Ma

Ni3(NO3)2(OH)4 has a high theoretical specific capacitance, low cost, and environmental friendliness, making it a promising electrode material. Specifically, Ni3(NO3)2(OH)4 electrodes have a larger layer spacing (c = 6.898 Å) than Ni(OH)2 electrodes since NO3− has a much larger ionic radius than OH−. The larger layer spacing stores more electrolyte ions, significantly improving the electrochemical activity of the electrodes. Additionally, the interlayer NO3− can enhance the structural stability of Ni3(NO3)2(OH)4. However, since Ni3(NO3)2(OH)4 has a higher molar mass than Ni(OH)2, it has a lower theoretical specific capacity. Consequently, Ni3(NO3)2(OH)4 has not been used in zinc-based alkaline batteries. Studies showed that doping could enhance the electrochemical performance of electrode materials. Therefore, this study used a simple solvothermal reaction to synthesize yttrium-doped Ni3(NO3)2(OH)4 (Y-Ni3(NO3)2(OH)4), assembling a Y-Ni3(NO3)2(OH)4//Zn battery for electrochemical testing. Y-Ni3(NO3)2(OH)4 served as the cathode in the battery. The analysis of Y-Ni3(NO3)2(OH)4 showed that yttrium (Y) doping increased the specific surface area and pore size of Ni3(NO3)2(OH)4 significantly. The increased specific surface area improved the active material utilization, and the abundant mesopores facilitated OH− transport, substantially enhancing the battery's specific capacity and energy density. Ultimately, the specific discharge capacity of the advanced Y-Ni3(NO3)2(OH)4//Zn battery reached 177.97 mA h g−1 at a current density of 4 A g−1, nearly doubling the capacity of the earlier Ni3(NO3)2(OH)4//Zn battery (103.59 mA h g−1).

研究领域: 材料科学 · 电化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Radiation synthesis of Ni3(NO3)2(OH)4 nanosheets for high-performance supercapacitor

Runfang Yang,Kai Zhang,Wei Yan,Chunyang Li,Yiwen Long,Maosheng Wu,Xiaolin Cheng,Hongwei Han,Xingguang Zhang,Mingxing Zhang,Guozhong Wu

Ni 3 (NO 3 ) 2 (OH) 4 positive electrode material was for the first time synthesized by gamma ray radiation under ambient conditions, and systematically investigated the synthesis mechanisms and electrochemical performance. The electrochemical performance of Ni 3 (NO 3 ) 2 (OH) 4 electrode can be regulated by controlling the absorbed dose. Ni 3 (NO 3 ) 2 (OH) 4 -200 kGy displays a remarkable electrochemical performance for supercapacitor, including a high specific capacity (1,086.7   C   g –1 at 1   A   g –1 ), good rate capability (50.6% at 15   A   g –1 ), fast Faraday reaction kinetics, and excellent electrochemical cycle stability (90.8% retention at 5   A   g –1 , after 5,000 cycles). Furthermore, the assembled Ni 3 (NO 3 ) 2 (OH) 4 -200 kGy//AC hybrid device exhibits a notable energy density of 99.8   Wh   kg –1 at a power density of 849   W   kg –1 (1   A   g –1 ), and excellent electrochemical cycle stability, retaining ~92.5% of its initial capacitance after 5,000 cycles at 1   A   g –1 . This work provides a new reaction pathway for the synthesis of inorganic materials and expands the potential application of radiation technology for electrode materials.

研究领域: 材料科学 · 电化学 · 纳米技术 · 辐射化学 · 储能
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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 56 ·期 4 ·3011-3023 · IF 3.553

Branched nanosheets-interlaced structure of Co2+/Co3+-doped Ni(OH)2 originating from Ni3(NO3)2(OH)4 template with significantly boosted electrochemical performance

Wang Jing,Li Jing,Liu Yuanyuan,Wang Meiri,Cui Hongtao

The cycling stability of electrode materials is a key for Faraday supercapacitors (FSs), especially the structure-unstable Ni(OH) 2 . There exist various strategies for stabilizing the structure of Ni(OH) 2 such as cobalt ions doping and mechanical support from substrate. However, these strategies have their own disadvantages. On the other hand, the combination of two or more strategies has the serious issues in materials synthesis. In this work, a branched nanosheets-interlaced structure of Co 2+ /Co 3+ -doped Ni(OH) 2 is built by a method of precursor template, which effectively applies two strategies including ions doping and self-supportive structure. Due to the synergistic contribution of these two strategies, the cycling stability of as-prepared material is significantly enhanced. This material also presents excellent high-rate capacity, and the as-assembled asymmetric supercapacitors (ASCs) show both high energy and power densities. These results prove that the effective combination of ions doping and self-supportive structure strategies is a promising route for the preparation of Ni(OH) 2 -based electrode materials with high performance.

研究领域: 材料科学 · 电化学
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Sustainable Energy & Fuels · 2020 ·Vol. 4 ·期 4 ·1780-1788 · IF 5.503

A branched nanosheet-interlaced structure of high performance Ni(OH)2 derived from the isostructural Ni3(NO3)2(OH)4 to clarify the role of structure self-supporting in cycling stability

Jing Wang,Jing Li,Meiri Wang,Yuanyuan Liu,Hongtao Cui

Battery-type electrode materials such as Ni(OH)2 applied in Faraday supercapacitors could present a low cycling stability due to the microstructure damage of materials, originating from their cyclic volume swelling and shrinking. It is well established that the structural stability of materials is crucial for their cycling stability. However, the lack of knowledge about the structural relevance of materials to their cycling stability somehow results in a chaotic understanding on the material design. In this study, we try to reveal the structural relevance by comparing an orderly built nanostructure with a randomly packed nanostructure using Ni(OH)2 as the target material. It is found that the branched nanosheet-interlaced nanostructure of Ni(OH)2 has its self-supportive function in favor of its structural stability, thus promoting its cycling stability. Also, the orderly nanostructured Ni(OH)2 presents high electrochemical performance due to the reduced interfacial charge-transfer resistance and Warburg resistance.

研究领域: 材料科学 · 电化学
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