Xiaomin Liu

ORCID: 0000-0001-7853-9258
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About
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Research Areas
  • Advancements in Battery Materials
  • Advanced Battery Materials and Technologies
  • Supercapacitor Materials and Fabrication
  • Advanced Battery Technologies Research
  • Thermal Expansion and Ionic Conductivity
  • Extraction and Separation Processes
  • Ferroelectric and Piezoelectric Materials
  • Bauxite Residue and Utilization
  • Advanced battery technologies research
  • Ionic liquids properties and applications
  • Conducting polymers and applications
  • Concrete and Cement Materials Research
  • Recycling and utilization of industrial and municipal waste in materials production
  • Electrophoretic Deposition in Materials Science
  • Magnesium Oxide Properties and Applications
  • Layered Double Hydroxides Synthesis and Applications
  • Marine and coastal ecosystems
  • Microwave Dielectric Ceramics Synthesis
  • Oceanographic and Atmospheric Processes
  • Metal and Thin Film Mechanics
  • Phase Equilibria and Thermodynamics
  • Solar and Space Plasma Dynamics
  • Diamond and Carbon-based Materials Research
  • MXene and MAX Phase Materials
  • Geophysics and Gravity Measurements

Nanjing Tech University
2014-2024

State Key Laboratory of Chemical Engineering
2024

East China University of Science and Technology
2024

Inner Mongolia Agricultural University
2023

Inner Mongolia University of Science and Technology
2021

Materials Science & Engineering
2020

Qingdao University
2017

The Ni-rich Co-poor layered cathode (LiNixCoyMn1–x–yO2, x ≥ 0.9) is a candidate for the next-generation lithium-ion batteries due to its high specific capacity and low cost. However, inherent structural instability slow kinetics of Li+ migration hinder their large-scale application. Mo doping proposed enhance crystal structure stability LiNi0.9Co0.05Mn0.05O2 ensure preservation spherical secondary particles after cycle. characterization results indicate that not only significantly relieves...

10.1021/acsami.3c16475 article EN ACS Applied Materials & Interfaces 2024-01-20

A novel graft copolymer solid electrolyte with a relatively high ionic conductivity, 10−3.9 S cm−1 at 30 °C and 10−3.1 80 °C, is prepared by free radical polymerization in this study. The polymer consists of methacrylate as the backbone mixture hexadecal (C16)–methoxyl terminated oligo(ethylene oxide) certain ratio side chains. Fourier transform infrared spectroscopy (FTIR) differential scanning calorimetry (DSC) analysis reveal that non-polar unit (C16) end-modification not only greatly...

10.1039/c2jm34270g article EN Journal of Materials Chemistry 2012-01-01

LiFePO4/C nanocomposites with excellent electrochemical performance is synthesized from nano-FePO4, generated by a novel method using confined area impinging jet reactor (CIJR). When discharged at 80 C (13.6 Ag−1), the delivers discharge capacity of 95 mA h g−1, an energy density 227 W kg−1 and power 34 kW kg−1.

10.1039/c3cc41922c article EN Chemical Communications 2013-01-01

Cobalt sulfide (Co4S3) is considered one of the most promising anode materials for lithium-ion batteries owing to its high specific capacity. However, some disadvantages, such as poor electrical conductivity and volume expansion, lead low rate capability may hinder practical applications. Herein, we firstly fabricated leaf-like hollow Co4S3/C nanosheet arrays growing on carbon cloth (h-Co4S3/C NA@CC) by a facile solution method combined with carbonization, sulfidation annealing treatments....

10.1039/d0dt03070h article EN Dalton Transactions 2020-01-01

Compared with LiFePO4, LiMnPO4 offers 20% higher energy density, but suffers from several orders lower electronic and ionic conductivity. The strategy usually adopted to overcome these intrinsic drawbacks is particle nanosizing mainly achieved by wet chemical methods or solid-state reactions in molten hydrocarbon, which are not suitable for scale-up. A novel, economic scalable method proposed, using a T type micro-channel reactor continuously precipitate nano-Mn3(PO4)2·3H2O the first time....

10.1039/c4ra01943a article EN RSC Advances 2014-01-01
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