Tian Wenhui, Ren Penggang, Hou Xin, Fan Baoli, Wang Yilan, Pei Lu, Wang Hongtao, Chen Zhengyan, Jin Yanlin
School of Materials Science and Engineering, Xi'an University of Technology, Xi'an 710048, PR China.
School of Materials Science and Engineering, Xi'an University of Technology, Xi'an 710048, PR China; The Faculty of Printing, Packaging Engineering and Digital Media Technology, Xi'an University of Technology, Xi'an 710048, PR China.
J Colloid Interface Sci. 2025 Jan;677(Pt B):626-636. doi: 10.1016/j.jcis.2024.08.112. Epub 2024 Aug 15.
Transition-metal phosphates/phosphides showcase significant promise for energy-related applications because of their high theoretical electrochemical characteristics. However, sluggish electro/ion transfer rates and kinetically unfavorable reaction sites hinder their application at high mass loading. Herein, a self-supporting electrode based on transition-metal phosphates was successfully fabricated via a one-step electrodeposition process. The nanosheet structure of transition-metal phosphates, formed by interconnecting nanoparticles, effectively mitigates the impact of stress and achieves a high mass-loading (21 mg cm) of the electrode. Additionally, the oxygen vacancy-rich and porous nanostructure of transition-metal phosphates endows the as-prepared electrodes with a significantly increased conductivity and fast ion migration rate for enhancing electrochemical kinetics. Consequently, the as-fabricated transition-metal phosphate electrode displays the highest areal specific capacity of 39.2F cm. Furthermore, the asymmetric supercapacitor achieves a maximum energy density of 0.79 mWh cm and a high capacity retention of 93.0 % for 10000 cycles under 60 mA cm. This work provides an ideal strategy for fabricating flexible electrodes with high mass loading and synthesizing transition-metal phosphate electrodes rich in oxygen vacancies.
过渡金属磷酸盐/磷化物因其高理论电化学特性而在能源相关应用中展现出巨大潜力。然而,缓慢的电子/离子转移速率和动力学上不利的反应位点阻碍了它们在高质量负载下的应用。在此,通过一步电沉积工艺成功制备了一种基于过渡金属磷酸盐的自支撑电极。由相互连接的纳米颗粒形成的过渡金属磷酸盐纳米片结构有效地减轻了应力影响,并实现了电极的高质量负载(21毫克/平方厘米)。此外,富含氧空位的多孔过渡金属磷酸盐纳米结构赋予所制备的电极显著提高的电导率和快速的离子迁移速率,以增强电化学动力学。因此,所制备的过渡金属磷酸盐电极展现出39.2法拉/平方厘米的最高面积比容量。此外,不对称超级电容器在60毫安/平方厘米下实现了0.79毫瓦时/平方厘米的最大能量密度和10000次循环93.0%的高容量保持率。这项工作为制备高质量负载的柔性电极以及合成富含氧空位的过渡金属磷酸盐电极提供了理想策略。