Miaomiao Liang, Maosen Hu, Yiwei Si, Rui Xue, Yongxia Kang, Hemeng Zhang, Haiyang Wang, Zongcheng Miao and Chong Fu
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In this work, we chose an iron-doped heterogeneous structured VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small> with a rich heterojunction interface and stability as a research object to test its application in ammonium ion storage. <em>Ex situ</em> XRD and <em>ex situ</em> FTIR tests proved that a phase transition happened during the first charge/discharge process. DFT calculations revealed that iron ion doping can adjust the electronic band structure and promote the phase transition by inducing fast catalytic coupling and NH<small><sub>4</sub></small><small><sup>+</sup></small> insertion process. Impressively, Fe-VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small> delivered superior electrochemical performance with high capacity and cycling stability when the atomic content of Fe was 0.1. The assembled Fe<small><sub>0.1</sub></small>VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small>//PTCDI full cell exhibited a high capacity of 143.8 mA h g<small><sup>−1</sup></small> at 0.5 A g<small><sup>−1</sup></small> and energy density of 115.1 W h kg<small><sup>−1</sup></small> and behaved much better than other full cells with different Fe doping content. This work provides a new strategy to design a high-performance electrode material for ammonium ion storage through heterojunction engineering and ion doping.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 5","pages":" 1397-1409"},"PeriodicalIF":9.2000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heterogeneous structure engineering and optimizing the electronic band structure of the VO2(B)/V3O5 cathode: toward a low-cost, long life span and green aqueous ammonium ion battery†\",\"authors\":\"Miaomiao Liang, Maosen Hu, Yiwei Si, Rui Xue, Yongxia Kang, Hemeng Zhang, Haiyang Wang, Zongcheng Miao and Chong Fu\",\"doi\":\"10.1039/D4GC04785K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Aqueous ammonium ion batteries are promising because of their high safety and efficient charge transfer rate in energy storage applications, but their wide applicability is hindered by the limited properties of the cathode materials. Heterojunction engineering and ion doping are effective strategies for enhancing the reaction dynamics and structural stability of cathode materials. In this work, we chose an iron-doped heterogeneous structured VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small> with a rich heterojunction interface and stability as a research object to test its application in ammonium ion storage. <em>Ex situ</em> XRD and <em>ex situ</em> FTIR tests proved that a phase transition happened during the first charge/discharge process. DFT calculations revealed that iron ion doping can adjust the electronic band structure and promote the phase transition by inducing fast catalytic coupling and NH<small><sub>4</sub></small><small><sup>+</sup></small> insertion process. Impressively, Fe-VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small> delivered superior electrochemical performance with high capacity and cycling stability when the atomic content of Fe was 0.1. The assembled Fe<small><sub>0.1</sub></small>VO<small><sub>2</sub></small>(B)/V<small><sub>3</sub></small>O<small><sub>5</sub></small>//PTCDI full cell exhibited a high capacity of 143.8 mA h g<small><sup>−1</sup></small> at 0.5 A g<small><sup>−1</sup></small> and energy density of 115.1 W h kg<small><sup>−1</sup></small> and behaved much better than other full cells with different Fe doping content. 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引用次数: 0
摘要
水铵离子电池以其高安全性和高效率的电荷传输速率在储能领域具有广阔的应用前景,但其正极材料性能的限制阻碍了其广泛的应用。异质结工程和离子掺杂是提高阴极材料反应动力学和结构稳定性的有效策略。本文选择具有丰富异质结界面和稳定性的铁掺杂异质结构VO2(B)/V3O5作为研究对象,测试其在铵离子存储中的应用。非原位XRD和非原位FTIR测试证明,在第一次充放电过程中发生了相变。DFT计算表明,铁离子掺杂可以通过诱导快速催化偶联和NH4+插入过程来调节电子能带结构,促进相变。当Fe的原子含量为0.1时,Fe- vo2 (B)/V3O5具有高容量和循环稳定性的优异电化学性能。制备的Fe0.1VO2(B)/V3O5//PTCDI全电池在0.5 a g−1下的容量为143.8 mA h g−1,能量密度为115.1 W h kg−1,性能优于其他不同Fe掺杂量的全电池。本研究为通过异质结工程和离子掺杂设计高性能铵离子存储电极材料提供了新的思路。
Heterogeneous structure engineering and optimizing the electronic band structure of the VO2(B)/V3O5 cathode: toward a low-cost, long life span and green aqueous ammonium ion battery†
Aqueous ammonium ion batteries are promising because of their high safety and efficient charge transfer rate in energy storage applications, but their wide applicability is hindered by the limited properties of the cathode materials. Heterojunction engineering and ion doping are effective strategies for enhancing the reaction dynamics and structural stability of cathode materials. In this work, we chose an iron-doped heterogeneous structured VO2(B)/V3O5 with a rich heterojunction interface and stability as a research object to test its application in ammonium ion storage. Ex situ XRD and ex situ FTIR tests proved that a phase transition happened during the first charge/discharge process. DFT calculations revealed that iron ion doping can adjust the electronic band structure and promote the phase transition by inducing fast catalytic coupling and NH4+ insertion process. Impressively, Fe-VO2(B)/V3O5 delivered superior electrochemical performance with high capacity and cycling stability when the atomic content of Fe was 0.1. The assembled Fe0.1VO2(B)/V3O5//PTCDI full cell exhibited a high capacity of 143.8 mA h g−1 at 0.5 A g−1 and energy density of 115.1 W h kg−1 and behaved much better than other full cells with different Fe doping content. This work provides a new strategy to design a high-performance electrode material for ammonium ion storage through heterojunction engineering and ion doping.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.