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Crystallization Modulation and Holistic Passivation Enables Efficient Two‑Terminal Perovskite/CuIn(Ga)Se_(2)Tandem Solar Cells

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Nano-Micro Letters 2025年第1期17卷 205-215页

作者： Cong Geng Kuanxiang Zhang Changhua Wang Chung Hsien Wu Jiwen Jiang Fei Long Liyuan Han Qifeng Han Yi‑Bing Cheng Yong Peng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070People’s Republic of China Triumph Photovoltaic Materials Co. Ltd.No.1001 Yannan AvenueHigh‑Tech Development DistrictBengbuAnhui 233000People’s Republic of China College of Materials Science and Engineering Guilin University of TechnologyGuilin 541004People’s Republic of China State Key Laboratory of Metal Matrix Composites Shanghai Jiao Tong UniversityShanghai 200240People’s Republic of China

Two-terminal(2-T)perovskite(PVK)/CuIn(Ga)Se_(2)(CIGS)tandem solar cells(TSCs)have been considered as an ideal tandem cell because of their best bandgap matching regarding to Shockley–Queisser(S–Q)***,the nature of the irregular rough morphology of commercial CIGS prevents people from improving tandem device *** this paper,D-homoserine lactone hydrochloride is proven to improve coverage of PVK materials on irregular rough CIGS surfaces and also passivate bulk defects by modulating the growth of PVK *** addition,the minority carriers near the PVK/C60 interface and the incompletely passivated trap states caused interface recombination.A surface reconstruction with 2-thiopheneethylammonium iodide and N,N-dimethylformamide assisted passivates the defect sites located at the surface and grain ***,LiF is used to create this field effect,repelling hole carriers away from the PVK and C60 interface and thus reducing *** a result,a 2-T PVK/CIGS tandem yielded a power conversion efficiency of 24.6%(0.16 cm^(2)),one of the highest results for 2-T PVK/CIGS TSCs to our *** validation underscores the potential of our methodology in achieving superior performance in PVK/CIGS tandem solar cells.

关键词： PVK/CIGS TSCs Irregular rough surfaces Modulating the growth PVK/C60 interface recombination

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[email protected] structured fillers for increasing dielectric constant and suppressing dielectric loss of PVDF-based composite films

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Ceramics International 2022年第16期48卷 22691-22698页

作者： Dajun Hou Jing Zhou Wen Chen Pengchao Zhang Jie Shen Zelang Jian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 PR China

High dielectric constant polymer dielectrics have attracted a great deal of attention in flexible electronics. However, it appears to be a paradox for polymer dielectrics that the enhancement of their dielectric constant often comes along with the increase of dielectric loss. Hence, we reported [email protected] shell structured filler/poly(vinylidene fluoride) (PVDF) composites to overcome this paradox. The hybrid filler with BaTiO 3 (BT) as the core, conductive carbon as the inner shell, and insulating polydopamine (PDA) as the outer shell was synthesized. As a result, the [email protected] @PDA/PVDF composites at the filler content of 11 vol% exhibit an outstanding dielectric performance with a dielectric constant of 45 and a dielectric loss of 0.053 at 10 3 Hz. This phenomenon can be attributed to the increased interfacial polarization induced by the inner carbon shell and the conductive paths blockade caused by the outside PDA shell inside the [email protected] @PDA/PVDF composites. This work reveals that rational design of [email protected] shell structured hybrid fillers maybe a promising way to optimize the overall dielectric performance of the PVDF-based composites.

关键词： [email protected] Dielectric constant Dielectric loss PVDF-based composites

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Electrolyte Engineering Toward High-Voltage Aqueous Energy Storage Devices

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Energy & Environmental materials 2021年第3期4卷 302-306页

作者： Jianfeng Tan Jinping Liu School of Chemistry Chemical Engineering and Life Science and State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China State Center for International Cooperation on Designer Low-carbon&Environmental Materials and School of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001China

Aqueous electrochemical energy storage(EES)devices are highly safe,environmentally benign,and inexpensive,but their operating voltage and energy density must be increased if they are to efficiently power multifunctional electronics,new-energy cars as well as to be used in smart *** Minireview summarizes the key breakthroughs and progress in expanding the electrochemical stability window(ESW)of aqueous EES devices over the past five *** briefly introducing the electrode engineering ways to widen ESW,we focus on four ground-breaking electrolyte engineering strategies and classify them into two kinds from the perspective of salts and exotic solutes/*** widening degree toward ESW of these emerging electrolytes is compared and the universal fundamental mechanism relating to the interactions between limited water molecules and high-concentration salts(or large amounts of exotic solutes/solvents)is *** challenges and perspectives for high-ESW electrolytes as well as recent advances in low-cost and other metal ion(sodium,potassium,zinc,etc.)-based electrolytes for expanding ESW are also outlined.

关键词： aqueous energy storage systems electrolyte engineering high voltage high-energy density water electrolysis

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Influence of pore size optimization in catalyst layer on the mechanism of oxygen transport resistance in PEMFCs

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Progress in Natural Science:materials International 2020年第6期30卷 839-845页

作者： Shumeng Guan Fen Zhou Jinting Tan Mu Pan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Hubei Provincial Key Laboratory of Fuel Cells Wuhan University of Technology

In PEMFC, the oxygen transport resistance severely hinders the cell from achieving high performance. In this paper, pore-forming agent was used to optimize the pore size distribution of the catalyst layer(CL), and to study its effect on the mechanism of oxygen transport resistance, including molecular diffusion resistance, Knudsen diffusion resistance, and local O2resistance in CL. The results showed that with the pore formation the cell performance had a significant improvement at high current density, mainly due to its better oxygen transport properties, especially under low platinum conditions. The addition of pore-forming agent moved the pore diameter toward a larger pore diameter with a range from 70 to 100 nm, and also obtaining a higher cumulative pore volume. It was found that the increase of the cumulative pore volume and larger pore size were conducive to the diffusion of oxygen molecules in CL, and the resistance caused by which was the dominant part in total transport resistance. Further tests indicated that the improvement of molecular diffusion resistance was much larger than that of Knudsen diffusion resistance in the catalyst layer after pore formed. In addition, the optimized pore structure will also get a higher number of effective pores, which resulted in an increased effective area of the ionomer on the Pt surface. The higher effective area of the ionomer was particularly beneficial for the reduction of local O2resistance with low Pt loading.

关键词： Pore size optimization Pore-forming agent Oxygen transport resistance PEMFC

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Structural Evolution and Thermoelectric Performance in (Gete)M(Sb2te3)N Compounds

SSRN

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SSRN 2024年

作者： Chen, Shuo Liu, Keke Luo, Tingting Liao, Lin Yang, Zhen Zhong, Shenlong Wu, Jinsong Su, Xianli Poudeu, Pierre Ferdinand Poudeu Zhang, Qingjie Tang, Xinfeng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Department of Materials Science and Engineering University of Michigan Ann ArborMI48109 United States

Exploring the relationship between crystal structure and thermoelectric performance is a pivotal topic in the thermoelectric field. In this study, we have conducted a comprehensive investigation on the correlation between the structural evolution of (GeTe)m(Sb2Te3)n pseudo-binary system and the thermoelectric properties. The proportion of van der Waals bonds increase with the rising Sb2Te3 content, resulting in an increase in the anisotropy of the electrical conductivity and a decrease in the average sound velocity. Additionally, the cation sites in the crystal lattice of these compounds exhibit a mixed occupancy of Ge/Sb atoms, although the cation sites adjacent to the van der Waals gaps are predominantly occupied by Sb atoms. The ultra-low lattice thermal conductivity of the GST124 and GST147 compounds is mainly attributed to the high concentration of van der Waals bonds and enhanced phonon scattering arising from Ge/Sb mixed cation occupancy and high density of defect structures. The high electrical conductivity combined with the low lattice thermal conductivity enables GST124 and GST147 compounds to achieve a maximum ZT value of 0.56 and 0.57, respectively. Higher thermoelectric performance can be achieved through optimization of the microstructure as well as the carrier concentration. © 2024, The Authors. All rights reserved.

关键词： Anisotropy

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Regulation of Dynamic Recrystallization in p-Type Bi2Te3-Based Compounds Leads to High Thermoelectric Performance and Robust Mechanical Properties

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SSRN 2024年

作者： Chen, Shuo Luo, Tingting Yang, Zhen Zhong, Shenlong Su, Xianli Yan, Yonggao Wu, Jinsong Poudeu, Pierre Ferdinand Poudeu Zhang, Qingjie Tang, Xinfeng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Department of Materials Science and Engineering University of Michigan Ann ArborMI48109 United States

Bi2Te3-based bulk materials are the best commercially available thermoelectric materials for near room temperature applications. However, the poor mechanical properties of zone melting material and inferior thermoelectric performance of powder metallurgical material restrict their large scale deployment. In this study, p-type Bi₂Te₃-based materials were prepared using the hot extrusion technique, and the underlying mechanisms for microstructure evolution were revealed. The hot extrusion speed significantly impacts the strain rate, an indicator to modulate the dynamic recrystallization (DRX) and grain growth, thereby effectively regulating the microstructures of samples. For the sample extruded at a speed of 1.0 mm min-1, the refined grain with an average grain size of 1.53 μm and an orientation factor F(110) of 0.28 is achieved. This highly textured structure and high-density low-angle boundaries (LAGBs) maintain the high carrier mobility of 264 cm2 V-1 s-1, comparable with the zone melting sample. In contrast, increasing grain boundaries, dislocations, and inherent point defects intensifies the phonon scattering and suppresses the lattice thermal conductivity to 0.73 W m-1 K-1. All these contribute to a practical high ZT value of 1.1 at room temperature. Moreover, the fine grains and high-density dislocations ensure robust mechanic properties with a compressive strength of 189 MPa and a bending strength of 139 MPa, which is a guarantee for the successful cutting of microparticles with dimensions of 100 × 100 × 200 μm3. The fabrication of high-quality materials with both high thermoelectric performance and strong mechanical properties paves the way for the miniaturization of thermoelectric modules. © 2024, The Authors. All rights reserved.

关键词： Textures

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通过表面终止化学设计实现高度可逆的锌金属阳极

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Science Bulletin 2023年第23期68卷 2993-3002,M0005页

作者：刘宇陈树麟袁豪熊方宇刘琴安永康张建勇吴璐孙建国 Yong-Wei Zhang 安琴友 John Wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Materials Science and Engineering National University of SingaporeSingapore 117574Singapore Institute of High Performance Computing Agency for ScienceTechnology and Research(A*Star)Singapore 138632Singapore Institute of Materials Research and Engineering(IMRE) Agency for ScienceTechnology and Research(A*Star)Singapore 138634Singapore

锌表面自然形成的非均匀氧化层(ZnO)会与电解液发生反应形成Zn_(4)(OH)_(6)SO_(4)·xH_(2)O(ZSH)副产物,导致锌负极表面非均匀沉积,从而阻碍水性锌离子电池实际应用.为了排除氧化层分布形式的影响,本文利用表面终止化学设计策略在... 详细信息

锌表面自然形成的非均匀氧化层(ZnO)会与电解液发生反应形成Zn_(4)(OH)_(6)SO_(4)·xH_(2)O(ZSH)副产物,导致锌负极表面非均匀沉积,从而阻碍水性锌离子电池实际应用.为了排除氧化层分布形式的影响,本文利用表面终止化学设计策略在锌负极表面制备了一层完全氧化的ZnO层,研究发现锌负极均匀分布的ZnO层会原位演化形成致密的ZSH功能层.均匀且致密的ZSH能够有效隔绝电解液的腐蚀,从而有效提高锌负极界面的稳定性.此外,ZSH(002)晶面边缘的不饱和悬空键(如-O)更容易和Zn(H_(2)O)_(6)^(2+)结构中的锌离子形成强Zn-O键,可以促进Zn(H_(2)O)_(6)^(2+)的脱溶剂化和锌离子沿边扩散,实现了高度可逆的锌沉积行为并限制了副反应.基于此,本文提出与“表面脱水-晶体通道转移”机制明显不同的“边缘脱水-沿边缘转移”锌离子输运新机制.更重要的是,基于此组装的全电池显示出高循环稳定性(超过1000次循环)和高库仑效率(99.07%),验证了其潜在的实际应用价值.

关键词： Zn-O termination Zn Anode Solid electrolyte interphase Dendrite-free Zn ion battery

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Stress corrosion behavior and mechanism of Ti6321 alloy with different microstructures in simulated deep-sea environment

SSRN

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SSRN 2024年

作者： Zhang, Huixia Zhang, Fan Hao, Fuyao Sui, Yongqiang Li, Wenju Li, Xiangbo Hou, Jian Guo, Weimin State Key Laboratory for Marine Corrosion and Protection Qingdao Luoyang Ship Material Research Institute Qingdao China State Key Laboratory of Advanced Technology For Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

The stress corrosion cracking (SCC) behaviors of Ti-6Al-3Nb-2Zr-1Mo (Ti6321, in wt.%) alloy samples with equiaxed microstructure (EM), bimodal microstructure (BM) and Widmanstätten microstructure (WM) in simulated 3000m deep sea environment were investigated using electrochemical tests, electron backscattered diffraction (EBSD), and so on. The results revealed that WM exhibits the best SCC resistance, which is attributed to its best self-healing ability, and is beneficial for the re-passivation of fresh metal at the crack tip. Besides, there is no obvious micro-texture region in WM, and α phase colonies hinder the dislocation movement, resulting in the lowest crack growth rate. © 2024, The Authors. All rights reserved.

关键词： Titanium alloys

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Articular cartilage and osteochondral tissue engineering techniques:Recent advances and challenges

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Bioactive materials 2021年第12期6卷 4830-4855页

作者： Wenying Wei Honglian Dai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Biomedical Materials and Engineering Research Center of Hubei ProvinceWuhan University of TechnologyWuhan430070China International School of Materials Science and Engineering Wuhan University of TechnologyWuhan430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan528200China

In spite of the considerable achievements in the field of regenerative medicine in the past several decades,osteochondral defect regeneration remains a challenging issue among diseases in the musculoskeletal system because of the spatial complexity of osteochondral units in composition,structure and *** order to repair the hierarchical tissue involving different layers of articular cartilage,cartilage-bone interface and subchondral bone,traditional clinical treatments including palliative and reparative methods have showed certain improvement in pain relief and defect *** is the development of tissue engineering that has provided more promising results in regenerating neo-tissues with comparable compositional,structural and functional characteristics to the native osteochondral *** in this review,some basic knowledge of the osteochondral units including the anatomical structure and composition,the defect classification and clinical treatments will be first *** we will highlight the recent progress in osteochondral tissue engineering from perspectives of scaffold design,cell encapsulation and signaling factor incorporation including bioreactor *** products for osteochondral defect repair will be analyzed and summarized ***,we will discuss the current obstacles and future directions to regenerate the damaged osteochondral tissues.

关键词： Osteochondral tissue engineering Cartilage tissue engineering Gradient scaffold Bioreactors

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Sulfur-linked carbonyl polymer as a robust organic cathode for rapid and durable aluminum batteries

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Journal of Energy Chemistry 2021年第12期30卷 320-327,I0007页

作者： Liang Fang Limin Zhou Lianmeng Cui Peixin Jiao Qinyou An Kai Zhang Department of Energy and Materials Engineering Dongguk University-SeoulSeoul 04620Republic of Korea Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Engineering Research Center of High-efficiency Energy Storage(Ministry of Education)Renewable Energy Conversion and Storage Center(RECAST)College of ChemistryNankai UniversityTianjin 300071China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200GuangdongChina

Rechargeable aluminum batteries are believed as a promising next-generation energy-storage system due to abundant low-cost Al sources and high volumetric specific *** Al-storage cathodes,however,are plagued by strong electrostatic interaction between host materials and carrier ions,leading to large overpotential and undesired cycling stability as well as sluggish ion diffusion ***,sulfur-linked carbonyl polymer based on perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA) as the cathode materials for ABs is proposed,which demonstrates a small voltage polarization(135 mV),a reversible capacity of 110 mAh g^(-1) at 100 mA g^(-1) even after 1200 cycles,and rapid Al-storage *** with PTCDA,the sulfide polymer possesses higher working voltage because of its lower LUMO energy level according to theoretical *** ordered carbonyl active sites in sulfide polymer contribute to the maximized material utilization and rapid ion coordination and dissociation,resulting in superior rate ***,the bridged thioether bonds endow the polysulfide with robust and flexible structure,which inhibits the dissolution of active materials and improves cycling *** work implies the importance of ordered arrangement of redox active moieties for organic electrode,which provides the theoretical direction for the structural design of organic materials applied in multivalent-ion batteries.

关键词： Aluminum batteries Organic materials Carbonyl polymer Electrochemical active sites Ordered arrangement

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