Materials Today Physics
·
2021
·
IF 9.298
C. Li,S. Ma,W. Cui,X. Sang,P. Wei,W. Zhu,X. Nie,W. Zhao,Q. Zhang
Seeking novel and effective approaches to synergistically improve the electrical and thermal transport properties and electro-thermal conversion efficiency of Bi 2 Te 3 -based alloys is essential for commercial applications. Here, GdCo 2 /Bi 0.37 Sb 1.63 Te 3 thermoelectric nanocomposites were designed and synthesized to achieve synergistic improvement of electrical and thermal properties . As confirmed by magnetoresistance measurement, the built-in magnetic field and magnetic scattering generated by magnetic nanoparticles decrease the carrier concentration and mobility, and increase the Seebeck coefficient . Meanwhile, GdCo 2 nanoparticles lead to broad-frequency phonon scattering, which effectively reduces the lattice thermal conductivity of nanocomposites. Eventually, the average ZT of the nanocomposite is increased by 18% in the range of 300–500 K, and the cooling temperature difference is increased by 68% near room temperature. This work proves that the thermoelectromagnetic coupling effects generated by magnetic particles can effectively improve the electro-thermal conversion performance.
研究领域:
材料科学
·
凝聚态物理
·
热电材料
·
纳米科技
·
功能材料
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2022
·Vol. 10
·期 23
·12429-12437
·
IF 14.511
Shuang Li,Yunxiang Hou,Di Li,Bo Zou,Qingtang Zhang,Yang Cao,Guodong Tang
SnSe is considered one of the most intriguing new thermoelectric materials. Polycrystalline SnSe offers a wide range of thermoelectric applications due to its facile synthetic processing and machinability. Herein, we have achieved a high average ZT of 0.8 as well as a high peak ZT of 1.86 in solution-synthesized porous Zn and Ga codoped SnSe nanosheets, generating a maximum energy conversion efficiency of 13.3%. High-density micro/nanopores are induced in the SnSe matrix, which are more effective for scattering phonons and reducing the thermal conductivity. The high density of micro/nanopores, nanosheet structure and dislocations contribute to an ultralow lattice thermal conductivity (0.157 W m−1 K−1 at 873 K). Meanwhile, Ga incorporation can induce band convergence and create resonance levels, producing a large Seebeck coefficient. Ga and Zn codoping contributes to a sharp increase in carrier concentration and an obviously increased electrical conductivity. The enhanced Seebeck coefficient and increased carrier concentration help in achieving a significant enhancement of the power factor over a wide temperature range in the porous Zn and Ga codoped SnSe nanosheets. Consequently, high thermoelectric performance is realized over a wide temperature range via the decoupling of electron–phonon transport in SnSe. This work opens up a great opportunity for designing prospective materials for thermoelectric applications with the aid of the solution synthesis route.
研究领域:
材料科学
·
凝聚态物理
·
纳米科技
·
能源材料
·
半导体物理
·
热电转换
·
无机功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Siqi Wang,Zhi Yang,Yuejun Sun,Yu Xiao,Li-Dong Zhao
PbTe-based thermoelectric materials are considered to be a medium-temperature thermoelectric candidates and the high-performance n -type PbTe is urgently to be developed to match its p -type counterpart on account of practical application. Herein, we firstly optimized the carrier density of n -type PbTe through Sb doping, and obtained a maximum ZT value of ∼1.0. Then, based on the optimized carrier density, we introduced ternary compounds AgSb(Se, Te) 2 to suppress the lattice thermal conductivity . Minimum lattice thermal conductivity of n -type PbTe was reduced as low as ∼0.53 W m −1 K −1 and ∼0.62 Wm −1 K −1 through introducing AgSbSe 2 and AgSbTe 2 , respectively. Combining the maintained electrical properties with suppressed thermal conductivity , maximum ZT values ∼1.2 and ∼1.3 were obtained in PbTe+2%AgSbSe 2 and PbTe+2%AgSbTe 2 , respectively. This work provides an effective strategy of synergistically balancing charge and phonon transports in n -type PbTe with ternary AgSb(Se, Te) 2 compounds.
研究领域:
材料科学
·
热电转换
·
凝聚态物理
·
半导体物理
·
功能材料
·
能量转换材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2021
·Vol. 32
·期 11
·14274-14285
·
IF 2.478
Gao Qianqian,Dai Yuqiang,Wei Xile,Zhou Changping,Gong Wenfeng,Song Haixiang,Guo Zhanhu,Li Chengbo
The Aurivillius compound Pb x Bi 6− x Fe 0.5 Co 0.5 Ti 4 O 18 thin films were prepared via chemical solution deposition method and the influence of Pb 2+ ions doping on the structure, ferroelectric and leakage properties were studied. With the increasing concentration of Pb 2+ ions, the lattice distortion is increased and the growth of the films along ab plane is promoted. The calculation results show that the internal stress of the films increases with the increase of Pb 2+ concentration. For the samples with low Pb 2+ doping concentration ( x < 0.6), the leakage current densities are also decreased, which can be attributed to the decrease in oxygen vacancy concentration. Due to the enhanced lattice distortion and decreased leakage current densities, the ferroelectric properties are improved. The film with x = 0.2 has a high saturation polarization of 42.3 µC/cm 2 . According to the fitting results, the leakage conduction mechanism is attributed to the combined effect of space-charge-limited conduction mechanism and ionic conduction mechanisms.
研究领域:
材料科学
·
凝聚态物理
·
功能材料
·
铁电学
·
薄膜制备
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Chenxi Wu,Huajun Lai,Feng Wang,Dianhui Wang,Weijiang Gan,Yulai She,Zhongmin Wang
V-based alloy membranes have huge potential for hydrogen separation and purification due to their higher hydrogen permeability , but suffer from hydrogen embrittlement . To address this matter, Pd and Fe have been chosen as alloying additions in V-based membranes to inhibit hydrogen embrittlement and maintain high hydrogen permeation performance based on the lattice-matching strategy. The phase structure, composition, microstructure and hydrogen permeation properties of V-Pd-Fe ternary alloy are investigated systematically, and the V-Fe and V-Pd binary alloys are presented for comparison. The results show that the prepared V-Pd-Fe ternary can match almost perfectly with pure V in lattice constants . Attributing to the lattice-matching strategy, the V-Pd-Fe ternary alloy exhibits more excellent hydrogen permeable properties than that of V-Fe and V-Pd binary alloys . The reduction of hydrogen embrittlement is ascribed to the lower hydrogen solubility that induced by the lattice distortion and electronegativity of Fe and Pd. Meanwhile, the manipulated lattice constant that parallel to pure V maintains high hydrogen permeation performance. Additionally, the designed ternary V 87.8 Pd 8 Fe 4.2 alloy exhibits exceptional long-term hydrogen permeation stability at 573 and 623 K, and hydrogen flux gradually decreases at 673 and 723 K is observed due to the interdiffusion between Pd film and V 87.8 Pd 8 Fe 4.2 substrate and defects in the Pd coating. This study offers new scenario and method for optimized hydrogen permeable properties and restrains hydrogen embrittlement in the alloy membrane.
研究领域:
材料科学
·
氢能与储能
·
金属膜分离技术
·
固态氢传输
·
合金设计
·
物理冶金学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Liang Zheng,Wenjie Zhang,Qi Wang,Hong Zhang,Zhou Yu,Cuihua Cheng,Yong Zhang,Ming Lei,Yong Zhao
MgB 2 bulks with NaCl doping amount ranging from 0–30 at% have been prepared by hot pressed sintering process . With the increase of NaCl doping amount, the c axis lattice parameter of MgB 2 monotonously increases, indicating the substitution of Mg atoms by larger Na atoms. Meanwhile, the intensity of diffraction peaks of both NaCl and impurity phase of MgO increases. More compact morphology was found in the NaCl doped MgB 2 samples. The critical transition temperature ( T c ) decreases from 38.2 K to 36.8 K with the increase of NaCl doping amount from 0 to 30 at%, and the corresponding transition width of T c (Δ T c ) increases from 0.5 K to 1.8 K. When the doping amount of NaCl is not exceeding 10 at%, the J c value is about 10 6 A/cm 2 at 4.2 K, 3 T, and 5 × 10 5 A/cm 2 at 10 K, 3T. J c performance of the 5 at% NaCl doped MgB 2 sample (NC05) reaches 6.8 × 10 5 A/cm 2 at 20 K, 2T, which improves approximately 20% compared to the pure one, attributing to the better grain connectivity of MgB 2 and enhancement of flux pinning force by NaCl doping.
研究领域:
凝聚态物理
·
材料科学
·
超导材料
·
无机固体化学
·
功能陶瓷
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Liang Chen,Dongmei Luo,Zhenghao Wang,Kejing Wu,Lei Song,Hongjiao Li,Shan Zhong,Siyang Tang,Bin Liang
Chemical looping hydrogen generation (CLHG) offers a promising solution for producing H 2 from industrial off-gas, such as blast furnace gas. However, increasing H 2 production capacity of the oxygen carrier (OC) at moderate temperature remains a significant challenge. In this study, a novel Cu-Fe-based OC is tailored for moderate-temperature CLHG from blast furnace gas. The results demonstrates that the tailored OC exhibits a superior H 2 production capacity of 12.99 mmol·g −1 at 550 °C, which is 6.5 times higher than that of Fe 2 O 3 at the same temperature. The addition of Cu leads to the formation of oxygen defects, which facilitate the migration of lattice oxygen, thereby the activity of the OC is enhanced. Furthermore, cyclical experiments demonstrates that O 2 -assisted regeneration strategy can effectively suppress the segregation of Cu during the cycling process, and the tailored OC shows good stability during 10 redox cycles. No additional separation process was required and the purity of the hydrogen was higher than 99%. The findings here open a new avenue for efficient CLHG from industrial off-gas at moderate operation temperature.
研究领域:
能源化学
·
材料科学
·
化学工程
·
工业气体利用
·
氢能技术
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 39
·19231-19240
·
IF 9.931
Minjie Xuan,Weidong Xiao,Hongjie Xu,Yonglong Shen,Zhenzhen Li,Shijie Zhang,Zhuo Wang,Guosheng Shao
The development of a solid electrolyte with superb Li+ conductivity is the key to enabling safe and high-performance all-solid lithium ion batteries which are free of the safety issues associated with flammable organic liquid electrolyte. Systematic experimental work has been carried out as a follow up to our recent theoretical prediction that superb ionic conductivity could be achieved through the tuning of the lattice chemistry in the cubic argyrodite Li6PS5Cl. Remarkable enhancement of the ionic conductivity has been achieved through the combined effect of excess Li and substitution of S with Te. This leads to an alloy, Li6.25PTe0.125S5.125Cl0.75, having the superb Li+ conductivity of 4.5 mS cm−1 at 25 °C, together with a low activation energy of 0.16 eV to safeguard adequate ionic conductivity at low temperature. This current work conclusively affirms the theoretical outcome that the superb ionic conductivity is attributed to weakened bonding, an enlarged unit cell, and a softened lattice, making it easier for the long-distance diffusion of Li+. In addition, this new class of solid electrolyte based on cubic chalcogenide is electrochemically compatible with the Li anode over a large potential window up to 7 V, which is highly desirable for high performance solid lithium ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
固体离子学
·
无机化学
✓ 已验证
DOI
高影响因子
Small
·
2023
·Vol. 20
·期 3
·2306251
·
IF 13.3
Muchun Guo,Ming Liu,Jianbo Zhu,Yuke Zhu,Fengkai Guo,Wei Cai,Yongsheng Zhang,QinYong Zhang,Jiehe Sui
Chemical bonds determine electron and phonon transport in solids. Tailoring chemical bonding in thermoelectric materials causes desirable or compromise thermoelectric transport properties. In this work, taking an example of CaMg 2 Bi 2 with covalent and ionic bonds, density functional theory calculations uncover that element Zn, respectively, replacing Ca and Mg sites cause the weakness of ionic and covalent bonding. Electrically, Zn doping at both Ca and Mg sites increases carrier concentration, while the former leads to higher carrier concentration than that of the latter because of its lower vacancy formation energy. Both doping types increase density-of-state effective mass but their mechanisms are different. The Zn doping Ca site induces resonance level in valence band and Zn doping Mg site promotes orbital alignment. Thermally, point defect and the change of phonon dispersion introduced by doping result in pronounced reduction of lattice thermal conductivity. Finally, combining with the further increase of carrier concentration caused by Na doping and the modulation of band structure and the decrease of lattice thermal conductivity caused by Ba doping, a high figure-of-merit ZT of 1.1 at 823 K in Zn doping Ca sample is realized, which is competitive in 1–2–2 Zintl phase thermoelectric systems.
研究领域:
材料科学
·
凝聚态物理
·
无机化学
·
能源材料
·
热电转换
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTRONIC MATERIALS
·
2024
·Vol. 53
·期 10
·6553-6562
·
IF 2.2
Zhang Yu,Ma Jianli,Chen Chen,She Yubin
In this work, non-stoichiometric Li 2(1+ x ) Mg 3 Ti 4 O 12 (L x MTO, x = 0.00–0.05) ceramics with excess lithium were prepared through a simple reaction sintering route to suppress lithium volatilization. According to the characterization of the phase composition and microscopic morphology of the pellets, single-phase L x MTO ceramics with a good microstructure were obtained. Excess lithium effectively inhibited the volatilization and optimized the morphology of the ceramics. A trend in relative density with an initial increase followed by a steep decrease was a predominant observation with the change in dielectric properties. The permittivity of the samples was dominated by the relative density and distortion of the [TiO 6 ] octahedron structure caused by Li + . The dielectric loss primarily originated from the refraction loss and scattering generated by pores, and the grain boundaries also contributed to the loss in the quality factor. Ultimately, at 1220°C, the Li 2.08 Mg 3 Ti 4 O 12 ceramics exhibited excellent microwave dielectric properties: ε r = 17.83, Q × f = 69,823 GHz and τ f = −18.19 ppm/°C.
研究领域:
材料科学
·
无机非金属材料
·
介电材料
·
陶瓷学
·
固态化学
·
电子材料
✓ 已验证
DOI
高影响因子
Small
·
2024
·Vol. 20
·期 45
·2403852
·
IF 13
Xinxin Wang,Chao Wang,Yajing Wang,Min Hao,Shengqiang Cui,Xudong Huang,Chunhui Wang,Jing Chen,Zhenxiang Cheng,Jianli Wang
N-type PbSe thermoelectric materials encounter challenges in improving the power factor due to the single-band structure near the Fermi level, which obstructs typical band convergence. The primary strategy for enhancing the thermoelectric figure of merit (ZT) for n-type PbSe involves reducing lattice thermal conductivity (κ lat ) by introducing various defect structures. However, lattice mismatches resulting from internal defects within the matrix can diminish carrier mobility, thereby affecting electrical transport properties. In this study, n-type AgCuTe-alloyed PbSe systems achieve a peak ZT value of ≈1.5 at 773 K. Transmission electron microscopy reveals nanoprecipitates of Ag 2 Te, the room temperature second phase of AgCuTe, within the PbSe matrix. Meanwhile, a unique semi-coherent phase boundary is observed between the PbSe matrix and the Ag 2 Te nanoprecipitates. This semi-coherent phase interface effectively scatters low-frequency phonons while minimizing damage to carrier mobility. Additionally, the dynamic doping effect of Cu atoms from the decomposition of AgCuTe within the matrix further optimize the high-temperature thermoelectric performance. Overall, these factors significantly enhance the ZT across the whole temperature range. The ZT value of ≈1.5 indicates high competitiveness compared to the latest reported n-type PbSe materials, suggesting that these findings hold promise for advancing the development of efficient thermoelectric systems.
研究领域:
材料科学
·
凝聚态物理
·
能源材料
·
纳米结构工程
·
热电转换
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Ranxi Liang,Chaozhu Shu,Anjun Hu,Minglu Li,Zhiqun Ran,Ruixin Zheng,Jianping Long
The sluggish oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) kinetics greatly limit the development of lithium-oxygen (Li-O 2 ) batteries. Therefore, developing efficient electrocatalysts with high stability to boost oxygen involved reactions is particularly important for promoting the application of Li-O 2 batteries. Here, CoSe 2 @NiSe 2 heterostructure with distinct heterogeneous interfaces was fabricated via deliberate interface engineering. The formation of heterogeneous interface promotes local fine atomic array distortion that can act as an additional active site of ORR/OER. In addition, CoSe 2 @NiSe 2 with a distinct heterogeneous interface is favorable for the formation of built-in electric field during charging/discharging to enable electrodes with fast electrical transfer rates and reaction kinetics. Synergistically, the additional active sites brought by the fine atomic array distortion are highly conducive to the reversible formation and decomposition of the product. Undoubtedly, batteries with CoSe 2 @NiSe 2 exhibit excellent discharge/charge capacity (3530.1 mA h g −1 and 3485.6 mA h g −1 ), low overpotential (1.21 V) and excellent electrochemical stability for over 1200 h.
研究领域:
材料科学
·
电化学
·
能源化学
·
纳米催化
·
电池技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）