硅酸盐学报

赝电容的起源和本体相赝电容的实现

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董韬文 ¹^,²^,³^,⁴ , 张伟 ¹^,²^,³^,⁴^,⁵^,⁶ , 郑伟涛 ¹^,²^,³^,⁴^,⁵

硅酸盐学报 | 国家自然科学基金重点项目中期成果专题—综合评述 2024,52(2): 442-453

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硅酸盐学报 |国家自然科学基金重点项目中期成果专题—综合评述 2024 , 52 (2) : 442 -453

赝电容的起源和本体相赝电容的实现

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董韬文¹^,²^,³^,⁴, 张伟¹^,²^,³^,⁴^,⁵^,⁶, 郑伟涛¹^,²^,³^,⁴^,⁵

作者信息

^1．吉林大学汽车仿真与控制国家重点实验室，长春 130012

^2．吉林大学材料科学与工程学院，长春 130012

^3．吉林大学汽车材料教育部重点实验室，长春 130012

^4．吉林省高效清洁能源材料国际科技合作重点实验室，长春 130012

^5．吉林大学未来科学国际合作联合实验室，长春 130012

^6．吉林大学电子显微镜中心，长春 130012

通讯作者:

张伟（1974—），男，博士，教授；

郑伟涛（1963—），男，博士，教授。

作者简介:

董韬文（1984—），男，博士，讲师。

Origin of Pseudocapacitance and Achieving Bulk Pseudocapacitance

Taowen DONG¹^,²^,³^,⁴, Wei ZHANG¹^,²^,³^,⁴^,⁵^,⁶, Weitao ZHENG¹^,²^,³^,⁴^,⁵

Affiliations

^1.Jilin University State Key Laboratory of Automotive Simulation and Control, Changchun 130012, China

^2.Jilin University School of Materials Science & Engineering, Changchun 130012, China

^3.Jilin University Key Laboratory of Automobile Materials (Ministry of Education), Changchun 130012, China

^4.Jilin Provincial International Cooperation Key Laboratory of High-Efficiency Clean Energy Materials, Changchun 130012, China

^5.Jilin University International Center of Future Science, Changchun 130012, China

^6.Electron Microscopy Center, Jilin University, Changchun 130012, China

Corresponding Author:

ZHANG Wei (1974-), male, Ph.D., Professor. E-mail: weizhang@jlu.edu.cn;

ZHENG Weitao (1963-), male, Ph.D., Professor. wtzheng@jlu.edu.cn

DONG Taowen (1984-), male, Ph.D., Lecturer. E-mail: twdong@jlu.edu.cn

出版时间: 2024-02-20 doi: 10.14062/j.issn.0454-5648.20230448

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摘要

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因兼具高能量密度、高功率密度和长循环寿命，赝电容材料引领了近年来超级电容器的发展。然而，赝电容材料仍面临着储能机制认知不足、未来发展方向模糊等挑战。本文基于国家自然科学基金重点项目“高能量/高功率电池型超级电容器-离子插层储能的电极材料构筑”的部分研究成果以及最新的文献报道，以典型赝电容材料为纲，简要回顾赝电容材料发展历史、重点讨论赝电容材料的储能机制、指出其储能机制中亟待厘清的问题。并在此基础上，提出赝电容材料未来发展的新思路-本体相赝电容，讨论了实现本体相赝电容的关键着力点和初步策略。

关键词

超级电容器 / 电极材料 / 储能机制 / 本体相赝电容

Abstract

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Electrochemical energy storage (EES) is an essential technology in modern lifestyle. As two typical EES devices, batteries and supercapacitors have their own advantages and disadvantages. Pseudocapacitive materials have attracted recent attention. Such materials store charges via battery-like redox reactions, but have supercapacitor-like electrochemical behaviors. Therefore, pseudocapacitive materials have a considerable potential to simultaneously achieve both high energy and high power density as well as excellent stability, merging a unbridgeable gap between batteries and supercapacitors. However, the development of pseudocapacitive materials still encounter some serious challenges such as unclear energy storage mechanism, lack of alternative pseudocapacitive materials and vague future development directions.

This review represented recent development on pseudocapacitive materials and briefly discussed their energy storage mechanism and the imperfections of the existing issues. Furthermore, we proposed a concept of bulk pseudocapacitance and realized a goal for the future development of pseudocapacitive materials. In addition, we also discussed some key factors and strategies for achieving such a bulk pseudocapacitance.

The energy storage mechanisms of pseudocapacitive materials were discussed. The first pseudocapacitive material, i.e., RuO₂ thin film, was reported by Trasatti et al. in 1971. The thin film electrode exhibited a supercapacitor-like cyclic voltammetry curve but differed from the electric double layer in faradic origin. Although the electrochemical performance of RuO₂ electrodes were enhanced via fabricating various nanostructures and introducing structural water, the energy storage mechanism of this electrode was not fully understood, and limited to reversible redox reaction at the surface, the content of structural water in crystal, fast proton transport and crystallinity of electrode, etc.. MnO₂ is another typical pseudocapacitive electrode, which was firstly reported by Lee and Goodenough in 1999. Simon and Gogotsi reported the pseudocapacitive response of this electrode to successive multiple surface redox reactions. Recently, Augustyn et al. indicated the pseudocapacitive response to the existence of nanoconfined interlayer structural water, mediating an interaction between charge carrier and electrode. Dunn et al. investigated the pseudocapacitive response for T-Nb₂O₅ electrode and proposed a model of pseudocapacitance, i.e., intercalation pseudocapacitance. Mxenes is one of pseudocapacitive materials with a unique structure that is responsible for its pseudocapacitive behaviors. Although it is still controversial whether it is a pseudocapacitive electrode, Co(OH)₂ demonstrates a coupled performance of batteries and supercapacitors. The energy storage mechanism of this electrode was investigated by in-situ X-ray adsorption spectroscopy. It was found that the high specific capacitance originates from a battery-mimic bulk reaction, while the high stability performance roots in the crystal structure stability in charge-discharge process. Furthermore, we highlighted that the Co(OH)₂ electrode blurs the distinction between supercapacitors and batteries, which is in accordance with the continuous transition from electric double layer to battery proposed by Fleischmann and co-workers. In future, more intensive studies should be conducted on the energy storage mechanism of pseudocapacitive materials, especially on the unique characteristics of charge carrier and electron transportation, charge transfer, interaction between charge carrier and electrode in an atom-level.

The energy density of pseudocapacitive materials is still far below than the actual demand, even the batteries. To address this issue, a concept of bulk pseudocapacitance is proposed. In fact, intercalation pseudocapacitance depicted by Dunn et al. is a typical example of bulk pseudocapacitance. Bulk pseudocapacitance refers to the pseudocapacitive response that happens throughout the bulk of the electrode material rather than the surface. Meanwhile, the proposal of bulk pseudocapacitance can provoke a research on boosting the pseudocapacitive response of battery materials to alleviate the lack of the alternative pseudocapacitive materials.

Reducing the size of active materials to nano-scale, i.e., nanostructured material, as one of the strategies, can be used to achieve the bulk pseudocapacitance. For instance, LiCoO₂ nanocrystalline with the sizes of ˂11 nm exhibits a pseudocapacitive response. In addition to nanostructured materials, a strategy named diffusionless-like conversion reaction to achieve pseudocapacitive response in conversion reaction was proposed. Based on the conversion reaction between Fe(OH)₂ and δ-FeOOH, a battery-like conversion reaction achieves a high specific capacitance, and a diffusionless-like transformation between charge and discharge phases without a massive atom movement presents high rate and stability performance.

For battery materials, their pseudocapacitive response can be enhanced via manipulating the charge carrier transport, electron transfer, and designing the interaction between charge carrier and electrode in atom-scale. In addition, such a provoking pseudocapacitive response in battery materials extends the scope of bulk pseudocapacitive materials. Li and co-workers enhanced the Li⁺ transport by pre-intercalation of NH₄⁺ into interplay of Mo₂CT_x. The mechanism of FeHCF storing NH₄⁺ is clarified, indicating that the weak Fe—N interaction mitigates the volumetric expansion induced by NH₄⁺ insertion. These findings demonstrate that modulating on charge carrier transport and interaction between charge carrier and electrode can improve the pseudocapacitive response of battery materials.

Summary and prospects

Future development of pseudocapacitance relies on a deep understanding of the energy storage mechanism of pseudocapacitive materials in an atomic level, i.e., the charge carrier and electron transport, charge transfer, and the interaction between charge carrier and electrode. In addition, exploiting and designing novel pseudocapacitive materials as well as boosting pseudocapacitive response of existing battery materials are crucial for the application of pseudocapacitive materials.

Key words

supercapacitor / electrode materials / energy storage mechanism / bulk pseudocapacitance

引用本文

董韬文, 张伟, 郑伟涛. 赝电容的起源和本体相赝电容的实现. 硅酸盐学报, 2024 , 52 (2) : 442 -453 . DOI: 10.14062/j.issn.0454-5648.20230448

Taowen DONG, Wei ZHANG, Weitao ZHENG. Origin of Pseudocapacitance and Achieving Bulk Pseudocapacitance[J]. Journal of the Chinese Ceramic Society, 2024 , 52 (2) : 442 -453 . DOI: 10.14062/j.issn.0454-5648.20230448

基金

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国家自然科学基金重点项目(51932003)

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2024年第52卷第2期

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文章信息

doi: 10.14062/j.issn.0454-5648.20230448

接收时间：2023-06-29
首发时间：2026-10-22
出版时间：2024-02-20

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收稿日期：2023-06-29
修回日期：2023-07-17

基金

国家自然科学基金重点项目(51932003)

作者信息

^1．吉林大学汽车仿真与控制国家重点实验室，长春 130012

^2．吉林大学材料科学与工程学院，长春 130012

^3．吉林大学汽车材料教育部重点实验室，长春 130012

^4．吉林省高效清洁能源材料国际科技合作重点实验室，长春 130012

^5．吉林大学未来科学国际合作联合实验室，长春 130012

^6．吉林大学电子显微镜中心，长春 130012

通讯作者:

张伟（1974—），男，博士，教授；

郑伟涛（1963—），男，博士，教授。

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https://castjournals.cast.org.cn/joweb/gsyxb/CN/10.14062/j.issn.0454-5648.20230448

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2种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

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