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Energy Technology · 2018 ·Vol. 6 ·期 11 ·2139-2145 · IF 3.175

Suppressing the Voltage Decay and Enhancing the Electrochemical Performance of Li1.2Mn0.54Co0.13Ni0.13O2 by Multifunctional Nb2O5 Coating

Wei Pan,Wenjie Peng,Guochun Yan,Huajun Guo,Zhixing Wang,Xinhai Li,Weihua Gui,Jiexi Wang,Ning Chen

This study focuses on suppressing the voltage decay and improving the electrochemical performance of Li-rich and manganese-based (LRM) material by Nb 2 O 5 coating, which is realized by an effective soft-chemical route using a mixture of ethanol and water as co-solvent. After Nb 2 O 5 coating, the resulted material demonstrates superior electrochemical performance as cathode material for LIBs. Particularly, it shows an excellent capacity retention of 98 % after 200 cycles at 1 C (1 C=250 mA g −1 ). Voltage decay within cycling is also obviously suppressed by Nb 2 O 5 coating. Moreover, it exhibits superior rate capacities, delivering 189 and 152 mAh g −1 at high current densities of 2 and 5 C, respectively. The improved electrochemical performance of Nb 2 O 5 coated sample can be attributed to that Nb 2 O 5 can suppress the phase transformation and voltage decay by acting as not only a fast ion conductor to accelerate the lithium ion diffusion at the cathode/electrolyte interface, but also an inert protective layer to reduce the direct contact between the cathode and electrolyte.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机非金属材料 · 固态离子学
✓ 已验证 DOI 高影响因子
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Solar RRL · 2021 ·Vol. 6 ·期 4 ·2100798 · IF 8.582

Controlling the Crystallographic Orientation of Sb2Se3 Film for Efficient Photoelectrochemical Water Splitting

Manjing Wang,Sanlong Wang,Qixing Zhang,Sanjiang Pan,Ying Zhao,Xiaodan Zhang

Finding a cost-effective semiconductor with commercial performance for photoelectrochemical (PEC) water splitting remains challenging. Sb 2 Se 3 , as a low-cost semiconductor, has excellent photo/electric properties for PEC water splitting. Via adjusting the Sb/Se ratio in the precursor ink, the Sb 2 Se 3 with favorable crystallographic orientation can be effectively controlled. The ink with an atomic ratio of Sb/Se = 1:3 induces the growth of a compact Sb 2 Se 3 film with a preferred orientation, resulting in rapid charge transport and high photocurrent. After depositing TiO 2 and Pt in turn, the photocathode with a structure of FTO/Au/Sb 2 Se 3 /TiO 2 /Pt exhibits a photocurrent density of 11.3 mA cm −2 at 0 V RHE . An unassisted solar water splitting device integrating the Sb 2 Se 3 -based photocathode with an inorganic perovskite photovoltaic cell achieves a solar-to-hydrogen efficiency of 2.45%. The efficient Sb 2 Se 3 -based photocathode shows promising potential for solar fuel production.

研究领域: 材料科学 · 物理化学 · 能源化学 · 半导体光电化学 · 可再生能源
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2018 ·Vol. 7 ·期 11 ·5991-6000 · IF 9.931

A bimetallic thermally regenerative ammonia-based battery for high power density and efficiently harvesting low-grade thermal energy

Weiguang Wang,Hua Tian,Gequn Shu,Dongxing Huo,Fang Zhang,Xiuping Zhu

A bimetallic thermally regenerative ammonia-based battery (B-TRAB) using inexpensive materials efficiently converts low-grade thermal energy into electricity with high power density. Through thermal regeneration of the anolyte, the B-TRAB system realized high-voltage discharge (1.38 V) with redox couples [Cu(II)/Cu and Zn(NH3)42+/Zn] and low-voltage charge (0.72 V) with Zn(II)/Zn and Cu(NH3)42+/Cu. Adding 2 M NH3 to the anolyte of a Cu/Zn-TRAB produced a peak discharge power density of 525 W m−2-electrode (120 W m−2-membrane), and the voltage (or current) and peak power could be doubled by connecting two cells in series (or parallel). In successive regeneration cycles, a maximum power density of 115 W m−2-electrode (26 W m−2-membrane) and a net energy density of 714 W h m−3 were produced at a constant current density of 100 A m−2. The power density was enhanced to 515 W m−2-electrode (118 W m−2-membrane) and maintained in successive cycles by adding acid to the regenerated catholytes, with a net energy density of 299 W h m−3 (discharged at a constant load of 12 Ω and charged at a constant current density of 100 A m−2). A thermal-electricity conversion efficiency of 0.95% (10.7% relative to the Carnot efficiency) was achieved.

研究领域: 能源材料 · 电化学工程 · 热电转换技术 · 可持续能源 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2024 ·Vol. 35 ·期 2 ·140 · IF 2.8

HEC/PAM hydrogel electrolyte toward regulating the surface of zinc negative electrode for inhibited dendrite in zinc-ion batteries

Ma Di,He Hao,Huang Xinglan,Wang Jingcheng,Hu Xuebu

The inhomogeneous plating/stripping of zinc and side reactions originating from the dissolution of the cathode material in water lead to the poor stability of zinc anode, which inevitably limits the practical application of zinc-based aqueous batteries. Therefore, a novel hydrogel electrolyte made of hydroxyethyl cellulose/polyacrylamide (HEC/PAM) with a 3D network-like structure is synthesized by radical polymerization and cross-linking reinforcement. Thanks to the porous crosslinked network and massive hydrophilic groups, the electrolyte has high ion conductivity of 3.17 × 10 –2  S cm −2 and decomposition voltage of 2.6431 V. The ion conductive hydrophilic groups facilitate the interfacial compatibility of the electrode with the electrolyte and stabilize zinc plating/stripping, which suppresses the formation of zinc dendrites. Meanwhile, the hydrogel electrolyte effectively alleviates the dissolution of the positive electrode and the occurrence of side reactions, and subsequently improves the stability of the electrode. As a result, the assembled Zn–Zn symmetric cell with HEC/PAM hydrogel electrolyte is stable without short circuit and rapid increase of overvoltage at 5 mA cm −2 . The polarization voltage of the assembled Zn–Cu half-cell is 59.2 mV and initial coulomb efficiency reaches 94.3%. The assembled Zn–V 2 O 5 ·nH 2 O/CNT full cell delivers an excellent cycling stability of 186.9 mAh g −1 at 0.5 A g −1 after 500 cycles with a high-capacity retention of 92.5% (only 52.1% in aqueous system). The new idea is provided for further development of functional hydrogel electrolytes in zinc-ion batteries.

研究领域: 电化学 · 能源材料 · 功能高分子 · 电池技术 · 界面化学
✓ 已验证 DOI 高影响因子
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International Journal of Electrochemical Science · 2023 ·Vol. 15 ·期 3 ·2528-2538 · IF 1.5

The Performance of a Novel PdFe/B-N-G Catalys for Ethanol Electro-oxidation in Alkaline Medium

Wenhui Geng,Mengmeng Zheng,Dan Chen,Xianwen Wang,Zekai Zhang,Yishan Lin,Dongqin Cai,Huiqin Li,Guobo Huang,Yanxian Jin Yu,Binbin Yus

Palladium catalyst (Pd) are made attention to application in alcohol fuel cells due to unique performance, as well as the resource abundance and low cost, but the catalyst performance and stability of the catalysts are still not satisfied. In this article, the novel PdFe/B-N-G catalysts with the double element alloying and dual-doping for ethanol electro-oxidation are successfully prepared and determined by XRD, TEM and XPS. TEM results reveal a relatively uniform and high dispersion of Pd particles is observed on PdFe/B-N-G catalyst. The XPS analysis indicates that Pd(0) contents of the PdFe/B-N-G catalyst are increased on account of the B, N-doping effect. Being explored as the catalyst to the ethanol oxidation reactions, the PdFe/B-N-G catalysts exhibit the better electrocatalytic activity with higher current densities and catalyst stability compared to those of PdFe/G and Pd/B-N-G, which can be attributed to the synergistic effect of the enhanced PdFe alloying and the B, N-doping, that can produce more activity sites dispersing on the surface of graphene. Thus, the novel PdFe/B-N-G catalysts can be the potential alternate in alcohol fuel cells.

研究领域: 电化学 · 纳米催化 · 能源材料 · 燃料电池 · 表面科学
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2012 · IF 3.832

Coaxial electrospun TiO2/ZnO core–sheath nanofibers film: Novel structure for photoanode of dye-sensitized solar cells

Pingfan Du,Lixin Song,Jie Xiong,Ni Li,Zhenqiang Xi,Longcheng Wang,Dalai Jin,Shaoyi Guo,Yongfeng Yuan

Novel TiO 2 /ZnO core–sheath nanofibers (NFs) film was fabricated through an extraordinary coaxial electrospinning technique . Dye-sensitized solar cells (DSSCs) were assembled using the TiO 2 /ZnO NFs film as photoanode . FESEM , TEM, FTIR , XRD , XPS and UV–vis were used to characterize the NFs electrode film. Photocurrent–voltage ( I – V ) characteristic, incident photo-to-current conversion efficiency (IPCE) spectrum, and electrochemical impedance spectroscopy (EIS) measurements were performed to evaluate the DSSCs performance. The results reveal that the DSSCs based on the TiO 2 /ZnO core–sheath NFs are superior to their bare TiO 2 NFs-based counterparts. Compared with the latter, the overall energy conversion efficiency was enhanced from 4.47 to 5.17%. And the possible mechanism for this enhancement was discussed.

研究领域: 材料科学 · 纳米技术 · 能源材料 · 光电化学 · 半导体薄膜
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2016 · IF 3.15

One-dimensional Fe2O3/TiO2 photoelectrode and investigation of its photoelectric properties in photoelectrochemical cell

Xi-Ming Song,Xin Zhou,Chunxue Yuan,Yu Zhang,Qiang Tong,Ying Li,Luxia Cui,Daliang Liu,Wei Zhang

We reported a novel Fe 2 O 3 /rutile TiO 2 nanorod (NR) arrays with the heterogeneous structure for photoelectrochemical (PEC) cells, which were fabricated on fluorine-doped tin oxide glass (FTO) substrates that serve as model architecture via a hydrothermal method. Fe 2 O 3 was revealed as an inexpensive and eco-friendly semiconductor sensitizer to make TiO 2 respond to visible light . By using this photoanode, the photoelectric conversion and water splitting properties of PEC cells based on the one-dimensional (1D) Fe 2 O 3 /TiO 2 heterostructures were investigated in detail under simulated sunlight. Meanwhile, the optimization of photovoltaic performance was also achieved by regulating the amount of Fe 2 O 3 . The open circuit voltage and short circuit current of the Fe 2 O 3 /TiO 2 solar cell can reach 0.435   V and 1.840   mA/cm 2 , respectively. In addition, theoretical analysis of the photoelectric effect is preliminarily explored on the basis of the flat band potential results.

研究领域: 材料科学 · 物理化学 · 能源科学 · 纳米科技 · 光催化
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

A multifunctional nano filler for solid polymer electrolyte toward stable cycling for lithium-metal anodes in lithium–sulfur batteries

XinLong Zhang,HaiYan Zhang,Yuan Geng,ZhangQin Shi,Sheng Zhu,QunJie Xu,YuLin Min

Lithium–sulfur (Li–S) batteries are considered as very promising energy storage systems due to their higher theoretical performance and lower active material cost. However, the notorious shuttle effect and lithium dendrite growth have severely restricted the industrial production of Li–S batteries. In this study, we used polyethylene oxide (PEO) as the matrix and added multifunctional nanofillers (nano In 2 O 3 ) to effectively inhibit the shuttle effect caused by the dissolution of lithium polysulphides (LiPSs) in Li–S batteries. As a multifunctional filler, nano-In 2 O 3 not only improves the ionic conductivity of the PEO electrolyte, but also forms a Li–In alloy layer in situ at the polymer/anode interface, which can cause the rapid diffusion of lithium ions and prevent the side reactions between lithium metal anode and the electrolyte. Achieving the effect of stabilizing the lithium metal anode and suppressing the shuttle effect. Multiple problems in the system are solved by introducing a single component with multiple functions. The symmetrical lithium battery based on the PEO/LiTFSI/In 2 O 3 solid polymer electrolyte (PEO/LiTFSI/In 2 O 3 SPE) has higher cycle stability (over 1200 h) because it is more stable to the lithium metal anode. The Li–S full battery also exhibits excellent electrochemical performance. After 500 cycles at 1C, its capacity can be maintained at 570 mAh g −1 , the capacity decay rate is 0.038%. The coulombic efficiency (CE) during the cycle is also close 100%.

研究领域: 电化学 · 能源材料 · 固态离子学 · 电池技术 · 纳米复合材料
✓ 已验证 DOI 高影响因子
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Materials Today Energy · 2022 · IF 9.257

Improvement of high-temperature energy storage performance in polymer dielectrics by nanofillers with defect spinel structure

Jing Fu,Mingcong Yang,Rui Wang,Sang Cheng,Xiaoyan Huang,Shaojie Wang,Junluo Li,Manxi Li,Jinliang He,Qi Li

The electrostatic energy storage performance of polymer dielectrics at high temperature and high electric field can be significantly improved by the incorporation of wide-bandgap, nano-sized particles. It is traditionally believed that the embedded nanoparticles can scatter the hot charges and lead to charge trapping in the interfacial region , which suppress the conduction loss and promote the energy storage performance. In this work, the nano-sized γ-Al 2 O 3 with cubic defect spinel structure and nano-sized α-Al 2 O 3 with a wider bandgap are introduced into a heat-resistant dielectric polymer, respectively, to form two different nanocomposites . The field-dependent energy storage performance, electrical conductivity , and breakdown strength of the polymer nanocomposites at high temperatures, as well as the thermally stimulated depolarization current , are investigated. The results indicate that the intrinsic deep traps introduced by γ-Al 2 O 3 with cubic defect spinel structure are a more critical factor in improving the energy storage performance of the polymer-based composites. We anticipate that our findings reported in this work may help to better guide the selection of nanofillers for high-temperature dielectric polymer nanocomposites.

研究领域: 材料科学 · 介电物理 · 高分子物理 · 能源材料 · 电气工程
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Interface engineering induced selenide lattice distortion boosting catalytic activity of heterogeneous CoSe2@NiSe2 for lithium-oxygen battery

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
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Indium doped sulfide solid electrolyte with tamed lithium dendrite and improved ionic conductivity for all-solid-state battery applications

Yuanyuan Li,Jun Cheng,Jianwei Li,Zhen Zeng,Yixuan Guo,Hongqiang Zhang,Hongbin Liu,Xiao Xu,Yiwei Rao,Deping Li,Lijie Ci

Sulfide solid state electrolytes capture much attention owing to their high conductivity and decent mechanical property. Nevertheless, the moisture instability and poor interfacial compatibility against lithium metal anode remain challenging and hinder the practical application. Herein, we report a novel indium (In) doping strategy based on the hard-soft-acid-base theory to tackle these issues. Optimized Li 7 P 2.9 S 10.9 In 0.1 electrolyte exhibits a high ionic conductivity of 4.1 × 10 −3  S cm −1 and achieves an enhanced interfacial compatibility. Importantly, as In partially replaces the phosphorus (P), the amount of released hydrogen sulfide can be significantly decreased and the air stability is improved. The all-solid-state battery assembled with the Li 7 P 2.9 S 10.9 In 0.1 electrolyte demonstrates a high discharge capacity and a good cycling stability under a high current density of 1.0 C. This work provides a practical and effective method to design sulfide-based solid-state electrolyte with high ionic conductivity and enhanced air stability for all-solid-state battery applications.

研究领域: 材料科学 · 电化学 · 能源存储 · 固态离子学 · 电池技术
✓ 已验证 DOI 高影响因子
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ORGANIC ELECTRONICS · 2019 · IF 3.495

Stable power output (PCE>19%) of planar perovskite solar cells with PbCl2 modification at the interface of SnO2/CH3NH3PbI3

Xin Qi,Ganghong Liu,Duo Wang,Ning Zhu,Yuqing Zhang,Zehao Zhang,Cuncun Wu,Xiangdong Li,Wei Luo,Yingqiang Li,Haozhe Hu,Zhijian Chen,Lixin Xiao,Shufeng Wang,Bo Qu

Interfacial modification as a feasible strategy to improve the properties of perovskite solar cells (PSCs) has been widely studied in recent years. In this work, PbCl 2 modification at the interface of SnO 2 /CH 3 NH 3 PbI 3 was used for CH 3 NH 3 PbI 3 -based planar PSCs. The introduction of PbCl 2 between SnO 2 and CH 3 NH 3 PbI 3 layers boosted the crystallization of perovskite film, which promoted the photovoltaic properties of corresponding PSCs. The open circuit voltage ( V OC ) and fill factor (FF) of the PbCl 2 -modified devices (1 mg/mL) were 1.11 V and 0.79, respectively, which were both higher than those of the reference devices without PbCl 2 (1.04 V and 0.76). Moreover, a steady-state power output efficiency exceeding 19% was obtained for the PbCl 2 -modified devices (1 mg/mL), which implied that PbCl 2 modification was an effective and low cost strategy for efficient PSCs.

研究领域: 材料科学 · 光伏技术 · 纳米科技 · 表面与界面工程 · 能源材料 · 半导体器件 · 功能材料
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