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CHEMICAL COMMUNICATIONS · 2015 ·Vol. 51 ·期 48 ·9785-9788 · IF 6.834

Fabrication of CeO2 nanotube supported Pt catalyst encapsulated with silica for high and stable performance

Chao Wan,Dang-guo Cheng,Fengqiu Chen,Xiaoli Zhan

This communication describes the fabrication of Pt/CeO2 nanotube@SiO2 core–shell catalysts applied to highly efficient water–gas shift reaction, where the initial CO conversion is 30.2% at 250 °C. Pt/CeO2 nanotube@SiO2 core–shell catalysts show outstanding thermal stability, even after accelerated aging under reaction conditions at 450 °C for 6 h, and the morphology is also unchanged after thermal treatment at 800 °C.

研究领域: 材料科学 · 催化化学 · 纳米技术 · 能源化学 · 环境催化
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Tailored Cu-Fe-based oxygen carrier for moderate-temperature chemical looping hydrogen generation from blast furnace gas

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
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Journal of Energy Chemistry · 2017 ·Vol. 27 ·期 2 ·413-418 · IF 2.594

DDQ as an effective p-type dopant for the hole-transport material X1 and its application in stable solid-state dye-sensitized solar cells

Yanyun Zhang,Xichuan Yang,Weihan Wang,Xiuna Wang,Licheng Sun

X1 (MeO-TPD) is an inexpensive and easily synthesized π -conjugated molecule that has been used as a hole-transport material (HTM) in solid-state dye-sensitized solar cells (ssDSSCs), achieving relatively high efficiency. In this paper, we characterize the physicochemical properties of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and show that it is a promising p-dopant in a spin-coating solution with X1 as the HTM. The doped ssDSSCs showed an increase in short-circuit current density from 5.38 mA cm –2 to 7.39 mA cm –2 , and their overall power conversion efficiency increased from 2.9% to 4.3%. Also, ssDSSCs with DDQ-doped X1 were more stable than the undoped samples, demonstrating that DDQ can act as a p-type dopant in X1 as an HTM for highly efficient, stable ssDSSCs.

研究领域: 材料科学 · 能源化学 · 光伏技术 · 纳米材料 · 半导体器件 · 表面化学 · 电化学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Overcoming polarization and dissolution of manganese-based electrodes to enhance stability in electrochemical lithium extraction

Yingjun Qiao,Yonggan Ran,Zhiqiang Qian,Bing Zhao,Chengpeng Li,Zhong Liu

The Mn dissolution issue in manganese-based materials (LMO) represents one of the most challenging barriers to further commercial development of electrochemical lithium extraction, which is an efficient and clean way of extracting Li from liquid resources. Here, by leveraging the advantages of composite materials, a novel combination of reduced graphene oxide (rGO) and sulfonated ionic polymers (Nafion) is introduced to relieve the issues of electrode polarization and manganese dissolution, critical factors limiting the durability of LMO electrodes. By modifying with rGO to enhance electronic conductivity and surface characteristics, and capturing dissolved Mn 2+ through Nafion, the modified electrode showed significant improvement in cycling stability and lithium adsorption capacity. Experimental results confirm that this synergistic approach effectively mitigates polarization effects and controls disproportionation reactions, thereby enhancing the stability of the lithium extraction process, revealing a notable increase in electrode capacity retention from 79.04 % to 94.64 % after 30 cycles. Additionally, through DFT calculations and XPS analysis, the effectiveness of the manganese capture strategy is validated. This work presents an effective new strategy to extend the lifespan of manganese-based electrodes and enhance their adsorption performance.

研究领域: 电化学 · 材料科学 · 能源化学 · 环境工程 · 无机化学
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ELECTROCHIMICA ACTA · 2015 · IF 4.504

Titanium Dioxide@Polyaniline Core-Shell Nanowires as High-Performance and Stable Electrodes for Flexible Solid-State Supercapacitors

Peng Zhang,Zhimeng Liu,Yuping Liu,Hongbo Fan,Yuanqi Jiao,Baiman Chen

In this work, we demonstrate a facile approach to synthesize high-performance and stable TiO 2 @PANI core-shell nanowires (NWs) as flexible electrodes for solid-state supercapacitors (SCs). The TiO 2 @PANI core-shell NWs are grown directly on highly conductive carbon cloth, which not only give efficient charge transport and accessible diffusion of the electrolyte, but also provide large surface area and active sites for redox reaction as well as good strain accommodation. Such these features enable them to deliver a large areal capacitance of 520.3   mF/cm 2 at 0.5   mA/cm 2 with outstanding rate capability. Furthermore, a flexible and stable solid-state SC device based on these TiO 2 @PANI core-shell NWs is also demonstrated. The as-fabricated solid-state SC device yields a remarkable volumetric capacitance of 898.4   mF/cm 3 , excellent flexibility and significant cycling stability with more than 97.2% retention of its capacitance after 10000 cycles. We believe that these findings may open up new opportunities to prepare high-performance PANI-based electrodes for flexible solid-state SCs.

研究领域: 材料科学 · 纳米科技 · 电化学 · 能源存储 · 功能材料 · 柔性电子学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 29 ·45093 · IF 1.86

Influences of diallyl phthalate as chain extender on the properties of high molecular weight poly(vinyl chloride) resin

Jianning Wu,Baoxun Sui,Lei Li,Guihua Meng,Xuhong Guo,Zhiyong Liu

A higher porosity with better thermostability is desirable for poly(vinyl chloride) (PVC) resin. In this study, high molecular weight PVC resins are prepared by vinyl chloride monomer (VCM)-diallyl phthalate (DAP) suspension copolymerization in a 20-L reactor at 50 °C using DAP as chain extender. SEM, BET, and analyses of plasticizer absorption results show the high molecular weight poly(vinyl chloride) (HPVC) by DAP-VCM copolymerization is loose and porous. With increasing DAP content when the mass ratio of DAP/VCM (ω ) is below the gel point, the porosity and the degree of polymerization increase. Nevertheless, the bulk density and particle size decrease. When more than the gel point, these relationships are reversed. Thermogravimetric analysis revealed that the HPVC had better thermostability than that of commercial PVC, and its thermostability increases with increasing ω before it reaches the gel point. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45093.

研究领域: 高分子化学 · 材料科学 · 聚合物合成 · 热分析 · 多孔材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Novel silicon/copper nanowires as high-performance anodes for lithium ion batteries

Juan Hong,Kun Cheng,Guiyin Xu,Myles Stapelberg,Yuan Kuai,Pengcheng Sun,Subing Qu,Zexin Zhang,Qidong Geng,Zhuangzhao Wu,Meifang Zhu,Paul V. Braun

Si/Cu/Zn ternary microspheres are prepared by a pulsed electrical discharging method in a scalable manner. Zn and partial Si within these microspheres can then be selectively removed by chemical etching to form Si/Cu nanowires. The Si/Cu (~62 atom% Si) nanowires show a high discharge capacity of 2092 mAh g −1 and a high capacity retention after 500 cycles at a current density of 200 mA g −1 . The excellent rate and cycling performance are attributed to the conductive Cu network and nanowire structure, which increases the electric conductivity of the electrode and accommodates the volumetric change of silicon during the charge/discharge process. Furthermore, the Si/Cu nanowire anode utilizes relatively cheap materials and flexible processing methods, costing approximately $0.3 g −1 . This work presents a novel method to prepare nanowire-like Si-based anode materials , which is promising to boost the yield of Si alloy NWs with low cost.

研究领域: 材料科学 · 电化学 · 纳米技术 · 能源存储 · 功能材料
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2023 ·Vol. 47 ·期 26 ·12109-12116 · IF 3.3

A Y-doped P2-Na0.6Li0.11Fe0.27Mn0.62O2 cathode with improved high-rate capability and cycling stability for Na-ion batteries

Ming-Hui Cao,Ren-Yan Li,Fen-Fen Huang,Xin-Yin Cai,Miao Cui,Shi-Ya Lin,Jing-Yang Tian,Yuan-Ping Jiang,Zulipiya Shadike,Zheng-wen Fu

P2-Na0.6Li0.11Fe0.27−xMn0.62YxO2 (x = 0, 0.5%, 1%, and 2%) cathode materials were successfully prepared using a traditional solid-state method with ball milling-assisted modification. The effect of Y-doping on the crystal structure, grain size, morphology and sodium storage performance of Na0.6Li0.11Fe0.27Mn0.62O2 was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), galvanostatic charge–discharge cycling tests, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results demonstrated that the ball-milling pre-treatment method could effectively reduce the grain size and mitigate the aggregation of Na0.6Li0.11Fe0.27Mn0.62O2. Additionally, reasonable Y-doping (x = 1%) significantly enhances the rate capability and cycling stability of Na0.6Li0.11Fe0.27Mn0.62O2via improving the Na+ diffusion kinetics and the reversibility of the oxygen redox reaction. These results indicate that Na0.6Li0.11Fe0.26Mn0.62Y0.01O2 is a promising candidate material for high-rate and long-life cathodes for Na-ion battery application.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机固体化学 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF LUMINESCENCE · 2022 · IF 4.171

A dual-mode self-referenced optical thermometry with high sensitivity based on Er3+-Yb3+ co-doped Sr2YTaO6 thermochromic phosphor

Yunkang Bu,Yu Chen,Xingyue Chen,Yichun Zhang,Degang Deng,Yuyu Shen,Liuyan Zhou,Chenwei Xu

Up conversion luminescent materials Sr 2 YTaO 6 : Er 3+ , Yb 3+ phosphors were prepared by high temperature calcination . In view of the formation, temperature characteristics , and photoluminescence features of the sample, X-ray diffraction and photoluminescence were used. Under the excitation at 980 nm, the series of samples is significantly stimulated by Er 3+ up-conversion luminescence and Yb 3+ sensitization at 524, 550 and 659 nm. According to the diversity of temperature sensing performance from these three highest peaks, a dual-mode temperature sensor on account of fluorescence intensity ratio (thermally coupled level between 2 H 11/2 and 4 S 3/2 , and nonthermally coupled energy levels between 2 H 11/2 and 4 F 9/2 ) is achieved by using a single luminescent center. Moreover, the phosphor has strong thermal stability, which is helpful to improve the accuracy of temperature measurement. Under the temperature measurement of a dual-mode temperature sensor, it is calculated that the optimal absolute sensitivity S a of thermally coupled energy level is 0.78 × 10 −3  K −1 (473 K) and relative sensitivity S r is 1.32 %K −1 (293 K), and the maximum optimal absolute sensitivity S a of non-thermally coupled energy level is 1.02 × 10 −4  K −1 (473 K) and relative sensitivity S r is 0.58 %K −1 (293 K). All results imply that Sr 2 YTaO 6 : Er 3+ , Yb 3+ phosphors are promising materials for self-referenced optical temperature measurement.

研究领域: 材料科学 · 光学工程 · 无机化学 · 功能材料 · 生物医学传感
✓ 已验证 DOI 高影响因子
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SOLID STATE IONICS · 2018 · IF 2.751

Cathode/electrolyte interface engineering via wet coating and hot pressing for all-solid-state lithium battery

Wenping Zha,Yinghui Xu,Fei Chen,Qiang Shen,Lianmeng Zhang

In this work, Li 7 La 3 Zr 2 O 12 (LLZO)-based membrane electrolyte, which has good flexibility and can be easily mass-produced, is proposed to address the intrinsic defects of ceramic electrolytes . The LLZO-based membrane electrolyte is electrochemically stable in the voltage range of 0–5.2 V vs. Li/Li + due to the good oxidative stability of LLZO. We also develop a simple and low-cost approach to fabricate the all-solid-state lithium battery (ASSLB). Wet coating and hot pressing are applied to form a continuous and homogeneous electrolyte layer on a cathode layer. Thanks to the integrated preparation process, there is no obvious interface between the cathode layer and the electrolyte layer, hence reducing the interface resistance. The Li/LiFePO 4 batteries exhibit desirable cycling performance at 60 °C, which deliver a maximum discharge specific capacity of 151.6 mAh·g −1 at 0.1C and maintain 97.8% of the capacity after 50 cycles.

研究领域: 材料科学 · 电化学 · 能源存储 · 固态离子学 · 先进电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Water cointercalation for high-energy-density aqueous zinc-ion battery based potassium manganite cathode

Tianjiang Sun,Qingshun Nian,Shibing Zheng,Xuming Yuan,Zhanliang Tao

Aqueous zinc-ion batteries (ZIBs) are gaining widespread attention owing to their intrinsic safety and low cost. However, it is still a challenge that finding robust cathode materials to build a high-energy-density aqueous ZIBs. Here, we synthesize a novel layered K 0.41 MnO 2 ·0.5H 2 O (KMO) cathode material for aqueous ZIBs. The constructed Zn//KMO battery shows an ultrahigh discharge capacity of 425 mAh g −1 and a remarkable energy density of 503 Wh kg −1 at 175 mA g −1 , as well as an good durability over 1500 cycles with no obvious capacity fading. A comprehensive study suggests that the water molecules can intercalate into layered KMO with H + and Zn 2+ ions during discharging process. The co-intercalating water not only facilitates ions insertion, but serves as pillars to stabilize the structure of KMO. This work demonstrates the mechanism about water cointercalation and provides a way for designing high-energy-density aqueous ZIBs.

研究领域: 电化学储能 · 材料科学 · 能源化学 · 无机化学 · 电池技术
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 33 ·18690-18697 · IF 2.936

Ultraflexible, stretchable and fast-switching electrochromic devices with enhanced cycling stability

Qian Liu,Zijie Xu,Wu Qiu,Chen Hou,Yanan Wang,Peijian Yao,Rui Yu,Wenxi Guo,Xiang Yang Liu

Ultraflexible electronics have received extensive attention due to their favorable properties, such as superior mechanical robustness, light weight and good compatibility with large-area roll-to-roll fabrication. Here we present a flexible sandwiched tungsten trioxide/silver nanotrough network/poly(3,4-ethylenedioxythiophene)–poly(styrene sulfonate) multi-layer transparent conducting electrode with prominent conductivity (sheet resistance as low as 1.08 Ω sq−1) and transparency (85%). In particular, the flexible transparent electrode exhibits excellent mechanical robustness upon bending and stretching. This hybrid electrode can be further adhered tightly to a layer of WO3 to form an electrochromic device, which simultaneously displays a rapid switching time (0.75 s/1.82 s for bleaching/coloring) and high cyclic performance (86% retention of the initial optical contrast after cycling for 30 000 s). In addition, our electrode can also be fabricated on various flexible substrates, such as polyethylene cling wrap, polydimethylsiloxane and Ecoflex, with sustained electrochromic properties after bending, twisting, stretching and even strong kneading. Our work provides new opportunities for the next generation of flexible and wearable electronics applied on various flexible substrates.

研究领域: 材料科学 · 纳米科技 · 柔性电子学 · 功能材料 · 电化学 · 高分子材料 · 器件物理
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