Shaoxiong Xie

Dr. Shaoxiong Xie

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2024 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
SCShuai Chen
Shuai Chen
TWTing Wang
Ting Wang
SXShaoxiong Xie
Shaoxiong Xie
JLJiaju Leng
Jiaju Leng
QZQingfeng Zhu
Qingfeng Zhu
QWQingyuan Wang
Qingyuan Wang

20 January 2024 in Advanced Functional Materials
Verified
Journal Article
Closed access
SXShaoxiong Xie
Shaoxiong Xie
QXQian Xu
Qian Xu
QCQiang Chen
Qiang Chen
JZJianguo Zhu
Jianguo Zhu
QWQingyuan Wang
Qingyuan Wang

17 May 2018 in Materials
Verified
Journal Article
Open access
PDF file
Yu ChenYu Chen
Yu Chen
JXJiageng Xu
Jiageng Xu
SXShaoxiong Xie
Shaoxiong Xie
ZTZhi Tan
Zhi Tan
RNRui Nie
Rui Nie
JZJianguo Zhu
Jianguo Zhu
Taking Bismuth Titanate (Bi4Ti3O12) as a Aurivillius-type compound with m = 3 for example, the ion (W6+/Cr3+) doping effect on the lattice distortion and interlayer mismatch of Bi4Ti3O12 structure were investigated by stress analysis, based on an elastic model. Since oxygen-octahedron rotates in the ab-plane, and inclines away from the c-axis, a lattice model for describing the status change of oxygen-octahedron was built according to the substituting mechanism of W6+/Cr3+ for Ti4+, which was used to investigate the variation of orthorhombic distortion degree (a/b) of Bi4Ti3O12 with the doping content. The analysis shows that the incorporation of W6+/Cr3+ into Bi4Ti3O12 tends to relieve the distortion of pseudo-perovskite layer, which also helps it to become more stiff. Since the bismuth-oxide layer expands while the pseudo-perovskite layer tightens, an analytic model for the plane stress distribution in the crystal lattice of Bi4Ti3O12 was developed from the constitutive relationship of alternating layer structure. The calculations reveal that the structural mismatch of Bi4Ti3O12 is constrained in the ab-plane of a unit cell, since both the interlayer mismatch degree and the total strain energy vary with the doping content in a similar trend to the lattice parameters of ab-plane.

31 July 2024 in Rare Metals
Verified
Journal Article
Closed access
PDF file
SCShuai Chen
Shuai Chen
TWTing Wang
Ting Wang
XWXiao‐Ling Wang
Xiao‐Ling Wang
KLKai Li
Kai Li
QZQing‐Feng Zhu
Qing‐Feng Zhu
SXShaoxiong Xie
Shaoxiong Xie

27 March 2018 in Materials
Verified
Journal Article
Open access
PDF file
SXShaoxiong Xie
Shaoxiong Xie
JXJiageng Xu
Jiageng Xu
Yu ChenYu Chen
Yu Chen
ZTZhi Tan
Zhi Tan
RNRui Nie
Rui Nie
JZJianguo Zhu
Jianguo Zhu
A sort of tungsten/chromium(W/Cr) co-doped bismuth titanate (BIT) ceramics (Bi4Ti2.95W0.05O12.05 + 0.2 wt % Cr2O3, abbreviate to BTWC) are ordinarily sintered between 1050 and 1150 °C, and the indentation behavior and mechanical properties of ceramics sintered at different temperatures have been investigated by both nanoindentation and microindentation technology. Firstly, more or less Bi2Ti2O7 grains as the second phase were found in BTWC ceramics, and the grain size of ceramics increased with increase of sintering temperatures. A nanoindentation test for BTWC ceramics reveals that the testing hardness of ceramics decreased with increase of sintering temperatures, which could be explained by the Hall–Petch equation, and the true hardness could be calculated according to the pressure-state-response (PSR) model considering the indentation size effect, where the value of hardness depends on the magnitude of load. While, under the application of microsized Vickers, the sample sintered at a lower temperature (1050 °C) gained four linearly propagating cracks, however, they were observed to shorten in the sample sintered at a higher temperature (1125 °C). Moreover, both the crack deflection and the crack branching existed in the latter. The hardness and the fracture toughness of BTWC ceramics presented a contrary variational tendency with increase of sintering temperatures. A high sintering tends to get a lower hardness and a higher fracture toughness, which could be attributed to the easier plastic deformation and the stronger crack inhibition of coarse grains, respectively, as well as the toughening effect coming from the second phase.

4 June 2025 in Physical Review Letters
Verified
Journal Article
Closed access
ZTZhi Tan
Zhi Tan
XLXiang Lv
Xiang Lv
LJLaiming Jiang
Laiming Jiang
XHXing Huang
Xing Huang
JXJie Xing
Jie Xing
JZJianguo Zhu
Jianguo Zhu
The origin of frequently observed ultrahigh electro-induced longitudinal strain, ranging from 1% to 26%, remains an open question. While recent studies have associated this phenomenon with bending deformation, the underlying mechanisms and the pronounced thickness dependence of the nominal strain have yet to be fully elucidated. Here, we demonstrate that the bending in piezoelectrics can be induced by a nonzero gradient of d_{31} across thickness direction. A scaling law (η_{3,nom}∝L^{2}E_{3}∇_{z}d_{31}/t) is derived to quantify the size dependence, thereby resolving longstanding ambiguities surrounding reported "giant" electrostrains. Simulations reveal that in standard perovskite piezoceramics, such as KNbO_{3}, a 0.69% concentration of oxygen vacancies can induce a 6.3 pC/N variation in d_{31} by suppressing polarization rotation, being sufficient to produce ultrahigh nominal strain in thin samples. Numerous factors, including gradients in defect concentration, composition, and stress, may lead to sufficient inhomogeneity in the distribution of d_{31}, suggesting electrobending may be a widespread phenomenon. This Letter presents a unified framework for understanding electrobending deformation, offering deeper insight into the mechanisms behind abnormally giant electrostrain responses in diverse piezoelectric systems and may encourage new engineering applications.