TY - JOUR
T1 - Rapid low-temperature densification of ZnO ceramics by cold sintering/spark plasma sintering with controlled transient liquid chemistry
AU - Zhao, Xuetong
AU - Wang, Jianglin
AU - Yang, Yang
AU - Wang, Qi
AU - Kang, Shenglin
AU - Li, Yuchen
AU - Yin, Guilai
AU - Liu, Hongwen
AU - Yang, Jindong
AU - Guo, Jing
N1 - Publisher Copyright:
© 2026 Elsevier Ltd and Techna Group S.r.l. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2026
Y1 - 2026
N2 - Conventional ceramic sintering generally requires high sintering temperatures, high energy consumption, and long processing time. To overcome these limitations, a rapid and highly efficient cold sintering/spark plasma sintering (CSP/SPS) is employed, with ZnO serving as a model system to systematically investigate the effects of different transient liquid phases, including water, CH3COOH and NaOH solution on the sintering behavior. ZnO shows appreciable solubility under both acidic and alkaline conditions. During CSP/SPS, the [Zn(CH3COO)]+ complex promotes ZnO reprecipitation more effectively than [Zn(OH)4]2-, leading to superior cold sintering performance in the CH3COOH system. A relative density exceeding 95% is achieved at 100 MPa/150 °C in the CH3COOH system, whereas the NaOH system requires more stringent conditions (150 MPa/200 °C) to reach comparable densification. Due to the limited solubility of ZnO in water, high densification is achieved only under more severe conditions (150 MPa/250 °C). The CSP/SPS approach leverages SPS-enabled rapid heating to preserve the transient liquid phase and thereby facilitate the dissolution-precipitation process during cold sintering. Systematic comparison of different transient liquid phases reveals that densification efficiency is governed by both solubility and precipitation kinetics. Enhanced electrical conductivity in wet compacts may enable localized charge transport, while electric-field-induced point defects and liquid-solid interfacial chemical defects enhance mass transport and accelerate densification. This work provides a mechanistically informed strategy for the low-temperature, energy-efficient fabrication of ceramic materials.
AB - Conventional ceramic sintering generally requires high sintering temperatures, high energy consumption, and long processing time. To overcome these limitations, a rapid and highly efficient cold sintering/spark plasma sintering (CSP/SPS) is employed, with ZnO serving as a model system to systematically investigate the effects of different transient liquid phases, including water, CH3COOH and NaOH solution on the sintering behavior. ZnO shows appreciable solubility under both acidic and alkaline conditions. During CSP/SPS, the [Zn(CH3COO)]+ complex promotes ZnO reprecipitation more effectively than [Zn(OH)4]2-, leading to superior cold sintering performance in the CH3COOH system. A relative density exceeding 95% is achieved at 100 MPa/150 °C in the CH3COOH system, whereas the NaOH system requires more stringent conditions (150 MPa/200 °C) to reach comparable densification. Due to the limited solubility of ZnO in water, high densification is achieved only under more severe conditions (150 MPa/250 °C). The CSP/SPS approach leverages SPS-enabled rapid heating to preserve the transient liquid phase and thereby facilitate the dissolution-precipitation process during cold sintering. Systematic comparison of different transient liquid phases reveals that densification efficiency is governed by both solubility and precipitation kinetics. Enhanced electrical conductivity in wet compacts may enable localized charge transport, while electric-field-induced point defects and liquid-solid interfacial chemical defects enhance mass transport and accelerate densification. This work provides a mechanistically informed strategy for the low-temperature, energy-efficient fabrication of ceramic materials.
KW - Cold sintering
KW - Densification behavior
KW - Joule heating
KW - Transient liquid phase
KW - ZnO ceramics
UR - https://www.scopus.com/pages/publications/105035412116
U2 - 10.1016/j.ceramint.2026.04.159
DO - 10.1016/j.ceramint.2026.04.159
M3 - 文章
AN - SCOPUS:105035412116
SN - 0272-8842
JO - Ceramics International
JF - Ceramics International
ER -