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学者姓名：汪浩
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Abstract ：
Electrochromic fabrics (ECFs) have demonstrated great potential in developing wearable products for applications in wearable displays and adaptive camouflage. Nonetheless, the lack of device integration usually makes ECFs not as flexible and lightweight as regular textiles. Herein, we developed a highly integrated all-in-one ECF by assembling all the essential components into a piece of nylon fabric. The configuration is based on EC-active polyaniline, Au reflector electrode and alumina counter electrode coating on both sides, and a gel electrolyte filling into the fabric. As a result, the all-in-one ECF has an ultrathin thickness of only 80 mu m, which offers flexibility superior to that of conventional ECFs. Stemming from the optical modulation between top PANI coating and a bottom Au reflector, the all-in-one ECF could deliver color switches between yellow and green, which are two typical environmental camouflage colors. It also demonstrates thermal management based on IR modulation behavior. Moreover, the dual-band optical modulation has excellent stability in response to mechanical bending, twisting, and tailoring. Considering excellent wearability and active optical modulation, the all-in-one ECF was further developed into an unmanned environmental adaptive camouflage prototype system by integrating with sensing and control modules, which exhibit fast color blending with dynamic environment background. The construction strategy of highly integrated ECFs proposed in this work could equally well apply to other EC-active materials and anticipated to provide new insights into developing high-performance intelligent applications, such as wearable displays and military camouflage clothing. The all-in-one ECF was exploited for an unmanned environment adaptive camouflage system.
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| GB/T 7714 | Fu, Guoxing , Gong, Hui , Xu, Jinheng et al. Highly integrated all-in-one electrochromic fabrics for unmanned environmental adaptive camouflage [J]. | JOURNAL OF MATERIALS CHEMISTRY A , 2024 , 12 (11) : 6351-6358 . |
| MLA | Fu, Guoxing et al. "Highly integrated all-in-one electrochromic fabrics for unmanned environmental adaptive camouflage" . | JOURNAL OF MATERIALS CHEMISTRY A 12 . 11 (2024) : 6351-6358 . |
| APA | Fu, Guoxing , Gong, Hui , Xu, Jinheng , Zhuang, Biying , Rong, Baoli , Zhang, Qianqian et al. Highly integrated all-in-one electrochromic fabrics for unmanned environmental adaptive camouflage . | JOURNAL OF MATERIALS CHEMISTRY A , 2024 , 12 (11) , 6351-6358 . |
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Abstract ：
Designing low-content and high-activity Pt-based catalysts with the high durability for the electrochemical hydrogen production remains a challenge. In this study, a ternary metal phosphide (NiCoP) with 1D nanowire (NW) and 2D nanosheet (NS) morphologies incorporating Pt clusters (denoted as Pt cluster -NiCoP@NF NWs and Pt cluster - NiCoP@NF NSs, respectively) was prepared using a hydrothermal -phosphorization -electrodeposition method. Based on the "tip effect " of NWs and a high electrochemical surface area, the as-prepared Pt cluster - NiCoP@NF NWs display better hydrogen evolution reaction (HER) performance, with a low overpotential of 65 mV at a high current density of 100 mA cm -2 and a low Tafel slope of 38.86 mV dec -1 , than the Pt cluster - NiC - oP@NF NSs, with an overportential of 95 mV at 42.53 mV dec -1 . This indicates that the NiCoP NW-based support exhibits faster HER kinetics. The mass activity (11.47 A mgPt - 1 ) of the Pt cluster -NiCoP@NF NWs is higher than that of commercial Pt/C catalysts. Significantly, the Pt cluster -NiCoP@NF NWs display excellent cyclic stability with negligible losses for 5000 cycles and 30-h tests at a high current of 500 mA cm - 2 .
Keyword ：
Tip effect Tip effect Pt nanoclusters Pt nanoclusters Metal-support interaction Metal-support interaction Ternary metal phosphide Ternary metal phosphide Hydrogen evolution reaction Hydrogen evolution reaction
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| GB/T 7714 | Ren, Dayong , Jiang, Daiyan , Huang, Yueshuang et al. Well-defined ternary metal phosphide nanowires with stabilized Pt nanoclusters to boost alkaline hydrogen evolution reaction [J]. | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2024 , 665 : 510-517 . |
| MLA | Ren, Dayong et al. "Well-defined ternary metal phosphide nanowires with stabilized Pt nanoclusters to boost alkaline hydrogen evolution reaction" . | JOURNAL OF COLLOID AND INTERFACE SCIENCE 665 (2024) : 510-517 . |
| APA | Ren, Dayong , Jiang, Daiyan , Huang, Yueshuang , Jin, Yuhon , Zeng, Chuitao , Zhou, Kailing et al. Well-defined ternary metal phosphide nanowires with stabilized Pt nanoclusters to boost alkaline hydrogen evolution reaction . | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2024 , 665 , 510-517 . |
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Abstract ：
Using the electrochemical technology to split water molecules to produce hydrogen is the key to obtain green hydrogen for solving the energy crisis. The large-scale application of hydrogen evolution reaction (HER) in water dissociation requires a highly active catalyst. In this paper, the highly dispersed PtCo bimetallic nanoparticles loading on MXene (PtCo/MXene) were prepared by using a step-to-step reduction strategy. The mentioned PtCo/MXene catalyst exhibits a high current density of -100 mA/cm2 in an acidic medium with just a 152 mV overpotential. In addition, the PtCo/MXene catalyst also displays a superior stability. Computational analysis and experimental testing demonstrate that the electronic interaction between Pt and Co can effectively modify the electronic structure of the active site, thereby enhancing the inherent catalytic performance of the material. More importantly, MXene two-dimensional nanosheets can expose more active sites because of their large specific surface area. Furthermore, MXene substrate with excellent electrical conductivity and harmonious interfaces between PtCo and MXene enhance charge transfer efficiency and lower the reaction activation energy.
Keyword ：
PtCo bimetallic PtCo bimetallic MXene MXene hydrogen evolution reaction (HER) hydrogen evolution reaction (HER)
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| GB/T 7714 | Chen, Guangxun , Zhang, Jian-hua , Zhou, Kai-Ling et al. MXene supported PtCo bimetallic catalyst for hydrogen evolution in acidic conditions [J]. | FRONTIERS IN ENERGY , 2024 , 18 (3) : 369-377 . |
| MLA | Chen, Guangxun et al. "MXene supported PtCo bimetallic catalyst for hydrogen evolution in acidic conditions" . | FRONTIERS IN ENERGY 18 . 3 (2024) : 369-377 . |
| APA | Chen, Guangxun , Zhang, Jian-hua , Zhou, Kai-Ling , Yang, Yang , Ma, Haoxiang , Jin, Yuhong et al. MXene supported PtCo bimetallic catalyst for hydrogen evolution in acidic conditions . | FRONTIERS IN ENERGY , 2024 , 18 (3) , 369-377 . |
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Abstract ：
Great progress has been made in the electrochromic (EC) technology with potential applications in various fields. As one of the most promising EC materials, Prussian blue (PB) has attracted great attention due to its excellent EC performance, such as low cost, easy synthesis, rich color states, chemical stability, suitable redox potential, and fast color-switching kinetics. This review summarizes the recent progress in PB electrodes and devices, including several typical preparation techniques of PB electrodes, as well as the recent key strategies for enhancing EC performance of PB electrodes. Specifically, PB-based electrochromic devices (ECDs) have been widely used in various fields, such as smart windows, electrochromic energy storage devices (EESDs), wearable electronics, smart displays, military camouflage, and other fields. Several opportunities and obstacles are suggested for advancing the development of PB-based ECDs. This comprehensive review is expected to offer valuable insights for the design and fabrication of sophisticated PB-based ECDs, enabling their practical integration into real-world applications.
Keyword ：
Prussian blue Prussian blue smart windows smart windows electrochromism electrochromism energy storage energy storage
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| GB/T 7714 | Zhang, Yongting , Li, Wanzhong , Gong, Hui et al. Recent progress in Prussian blue electrode for electrochromic devices [J]. | FRONTIERS IN ENERGY , 2024 . |
| MLA | Zhang, Yongting et al. "Recent progress in Prussian blue electrode for electrochromic devices" . | FRONTIERS IN ENERGY (2024) . |
| APA | Zhang, Yongting , Li, Wanzhong , Gong, Hui , Zhang, Qianqian , Yan, Liang , Wang, Hao . Recent progress in Prussian blue electrode for electrochromic devices . | FRONTIERS IN ENERGY , 2024 . |
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Abstract ：
Single-atom catalysts (SACs), as a thriving subfield of catalysis, have progressed tremendously. However, the contradiction between the isolated dispersion feature of metal sites and the high mass-specific activity of the catalyst inhibits the advances of the SACs. Herein, the Pt atoms are confined at the metallic Co phase edge in two-dimensional Co/Co(OH)(2) hierarchy structure (Pt-SA-Co@Co-Co(OH)(2)) by the defect inducted order electrode-position strategy. Both integrations of in-situ/ex-situ experimental characterizations and theoretical calculation reveal that such metal edge confined Pt atoms possess an enlarged atom exposure ratio, high stability, and the like-metal electronic state contributed by metal Co 3d, which enables the Pt atoms with more suitable affinity to simultaneously bind the multiple H atoms for durable H*-H-2 conversion and H-2 evolution. Moreover, the metallic PtSA-Co collaborated Co/Co(OH)(2) interfaces demonstrate a strong H2O dissociation capacity by the preference adsorption of H* on metallic Pt-SA-Co and OH*on Co/Co(OH)(2) interfaces. Combining a further enhancement of constructing the catalysts on an Ag nanowire network to form a seamlessly conductive nanostructure, the Pt-SA-Co@Co-Co(OH)(2) achieves a high mass activity with 5.92 A mg(-1) at the overpotential of 100 mV in alkaline condition, 37 times to that of the benchmark Pt/C catalyst and significantly outperforming the reported catalysts. While our work has focused on the hydrogen evolution reaction, this class of metal edge collaborated single-atom catalysts may be conducive to unlock the low mass-specific activity of atomically dispersed catalysts for various processes, such as oxygen evolution reactions (OER), CO2 reduction, and biomass conversion, etc.
Keyword ：
Hierarchy structure Hierarchy structure Multiple hydrogen conversion Multiple hydrogen conversion Metal edge Metal edge Single-atom catalysts Single-atom catalysts Confinement effect Confinement effect
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| GB/T 7714 | Zhang, Jianhua , Cai, JianYu , Zhou, Kai-Ling et al. Metal edge confined platinum atoms in metal/hydroxide hierarchy structure for multiple hydrogen conversion and evolution [J]. | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2024 , 358 . |
| MLA | Zhang, Jianhua et al. "Metal edge confined platinum atoms in metal/hydroxide hierarchy structure for multiple hydrogen conversion and evolution" . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY 358 (2024) . |
| APA | Zhang, Jianhua , Cai, JianYu , Zhou, Kai-Ling , Li, Hong-Yi , Liu, Jingbing , Jin, Yuhong et al. Metal edge confined platinum atoms in metal/hydroxide hierarchy structure for multiple hydrogen conversion and evolution . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2024 , 358 . |
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Abstract ：
Multicolor electrochromics have emerged as a promising solution for achieving active color modulation akin to chameleon-like adaptive camouflage. However, the development of electrochromics with full-color tunability still remains challenging, given the weak molecular polarity of inherent active materials and the difficulty in forming polarizer orbitals under varying applied voltages. Employing molecular polarity adjustments, a novel electrochromic polymer is successfully developed with a donor-gradient design of molecular architecture, enabling comprehensive full-color tunability. The polymer demonstrates outstanding overall electrochromic performance, including fast switching (around 1.4 s), high coloration efficiency (395.1 cm2 C-1@550 nm) and excellent reversibility (over 92% retention after 5000 cycles). Leveraging the full-color tunability and rapid response, the electrochromic polymer is further integrated with sensing and control modules to create an environmental adaptive camouflage prototype system capable of seamlessly blending colors with dynamic background environments. This work is expected to provide a straightforward approach for developing full-color electrochromics for electrochromic camouflage applications. An electrochromic polymer with donor-gradient architecture covers the full-color gamut and enables full-color tunability. This is the first time to deeply explore the full-color electrochromic mechanism in this material system. Leveraging full-color tunability and rapid response, the electrochromic polymer is integrated with sensing and control modules to create an environmental adaptive camouflage prototype device, seamlessly blending colors with dynamic backgrounds. image
Keyword ：
adaptive camouflage adaptive camouflage full-color modulation full-color modulation optoelectronic polymers optoelectronic polymers electrochromism electrochromism
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| GB/T 7714 | Li, Ang , Zhuang, Biying , Gong, Hui et al. Full-Color Electrochromics with Donor-Gradient Architectures for Chameleon-Like Adaptive Camouflage [J]. | ADVANCED OPTICAL MATERIALS , 2024 , 12 (21) . |
| MLA | Li, Ang et al. "Full-Color Electrochromics with Donor-Gradient Architectures for Chameleon-Like Adaptive Camouflage" . | ADVANCED OPTICAL MATERIALS 12 . 21 (2024) . |
| APA | Li, Ang , Zhuang, Biying , Gong, Hui , Xu, Jinheng , Zhang, Qianqian , Chen, Xiaoqing et al. Full-Color Electrochromics with Donor-Gradient Architectures for Chameleon-Like Adaptive Camouflage . | ADVANCED OPTICAL MATERIALS , 2024 , 12 (21) . |
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Abstract ：
一种电动自行车三元动力锂电池健康态和剩余寿命估算的方法，属于蓄电池寿命预测技术领域。研究电池在不同充放电打压范围内的循环曲线，利用Matlab软件对数据进行数据提取、模拟和分析，构建循环次数和充放电时间的对应的数学模型，不同的电压区间段对应不同的数学模型，由找出关系较强的充或放电电压区间对应的数学模型，采用此模型预测剩余寿命；本发明准确率高。
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| GB/T 7714 | 金玉红 , 李乐园 , 张建华 et al. 一种电动自行车三元动力锂电池健康态和剩余寿命估算的方法 : CN202310266671.1[P]. | 2023-03-14 . |
| MLA | 金玉红 et al. "一种电动自行车三元动力锂电池健康态和剩余寿命估算的方法" : CN202310266671.1. | 2023-03-14 . |
| APA | 金玉红 , 李乐园 , 张建华 , 张倩倩 , 刘晶冰 , 汪浩 . 一种电动自行车三元动力锂电池健康态和剩余寿命估算的方法 : CN202310266671.1. | 2023-03-14 . |
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Abstract ：
The construction of hydrogen evolution reaction (HER) catalysts at high current density (HCD) is challenging. Electron/mass transfer is hindered by the unsatisfied electrical conductivity at the catalyst-support interface and the massive gas bubbles adhered at the electrolyte-catalyst interface at HCD condition. Herein, a non-precious Ni2P@Cu3P heterostructure constructed by in-situ phase conversion is developed as an electrochemical HER catalyst. The Ni(OH)2 decorated Cu(OH)2 nanowire heterostructure is completely converted into the high electrical conductive Ni2P@Cu3P by a simple phosphatizing method, which not only remain the 3D nanowire array structure but also provide the large specific active surface area and plentiful channels for the fast charge/ mass transport to accelerate the HER dynamics. Furthermore, density functional theory calculations reveal that the strong electron interaction between the Ni2P and Cu3P, which can regulate the charge density distribution. As-prepared Ni2P@Cu3P heterostructure displays a more moderate free energy (& UDelta;GH2O = -0.37 eV and & UDelta;GH* = -0.01 eV) for alkaline HER. Benefiting from the complementary advantage of Ni2P and Cu3P, the Ni2P@Cu3P heterostructure exhibits an enhanced HER activity with an overpotential of 279 mV, an excellent long-term stability and durability at 1000 mA & BULL;cm- 2, providing the great potential for large-scale industrial applications.
Keyword ：
Electrocatalysis Electrocatalysis Heterostructure Heterostructure Hydrogen evolution reaction Hydrogen evolution reaction High current density High current density Transition metal phosphides Transition metal phosphides
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| GB/T 7714 | Zeng, Chuitao , Zhang, Jianhua , Jin, Yuhong et al. Accelerated mass/electron transfer by self-supporting Ni2P@Cu3P heterostructure array to boost alkaline hydrogen evolution at high current density [J]. | FUEL , 2023 , 350 . |
| MLA | Zeng, Chuitao et al. "Accelerated mass/electron transfer by self-supporting Ni2P@Cu3P heterostructure array to boost alkaline hydrogen evolution at high current density" . | FUEL 350 (2023) . |
| APA | Zeng, Chuitao , Zhang, Jianhua , Jin, Yuhong , Ren, Dayong , Li, Leyuan , Zhou, Kailing et al. Accelerated mass/electron transfer by self-supporting Ni2P@Cu3P heterostructure array to boost alkaline hydrogen evolution at high current density . | FUEL , 2023 , 350 . |
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Abstract ：
Zinc-air batteries (ZABs) are regarded as attractive devices for electrochemical energy storage and conversion due to their outstanding electrochemical performance, low price, and high safety. However, it remains a chal-lenge to design a stable and efficient bifunctional oxygen catalyst that can accelerate the reaction kinetics and improve the performance of ZABs. Herein, a phosphorus-doped transition metal selenide/carbon com-posite catalyst derived from metal-organic frameworks (P-CoSe2/C@CC) is constructed by a self-supporting carbon cloth structure through a simple solvothermal process with subsequent selenization and phosphati-zation. The P-CoSe2/C@CC exhibits a low overpotential of 303.1 mV at 10 mA cm-2 toward the oxygen evo-lution reaction and an obvious reduction peak for the oxygen reduction reaction. The abovementioned electrochemical performances for the P-CoSe2/C@CC are attributed to the specific architecture, the super-hydrophilic surface, and the P-doping effect. Remarkably, the homemade zinc-air battery based on our P-CoSe2/C@CC catalyst shows an expected peak power density of 124.4 mW cm-2 along with excellent cycling stability, confirming its great potential application in ZABs for advanced bifunctional electrocatalysis.(c) 2022 Elsevier Inc. All rights reserved.
Keyword ：
Zinc-air battery Zinc-air battery Phosphorus doping Phosphorus doping Bifunctional oxygen catalyst Bifunctional oxygen catalyst Metal-organic frameworks Metal-organic frameworks Cobalt selenide Cobalt selenide
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| GB/T 7714 | Mi, Hongtian , Li, Leyuan , Zeng, Chuitao et al. Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries [J]. | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2023 , 633 : 424-431 . |
| MLA | Mi, Hongtian et al. "Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries" . | JOURNAL OF COLLOID AND INTERFACE SCIENCE 633 (2023) : 424-431 . |
| APA | Mi, Hongtian , Li, Leyuan , Zeng, Chuitao , Jin, Yuhong , Zhang, Qianqian , Zhou, Kailing et al. Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries . | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2023 , 633 , 424-431 . |
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Abstract ：
一种自适应伪装的电致变色系统，基于新型电致变色织物可穿戴显示系统属于电控及新材料领域，包括电致变色织物、环境监测颜色传感系统和电源控制系统；可选地，电致变色织物由电致变色材料、电解质、对电极组成，在所述电源控制系统和电致变色织物连接时，所述电致变色织物呈不同颜色状态与环境相适应。在可穿戴、军事、防伪等众多领域有着巨大的应用潜力和价值。
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| GB/T 7714 | 汪浩 , 付国兴 , 龚辉 et al. 一种自适应伪装的电致变色系统 : CN202310296355.9[P]. | 2023-03-23 . |
| MLA | 汪浩 et al. "一种自适应伪装的电致变色系统" : CN202310296355.9. | 2023-03-23 . |
| APA | 汪浩 , 付国兴 , 龚辉 , 李万忠 , 白婷 , 张倩倩 et al. 一种自适应伪装的电致变色系统 : CN202310296355.9. | 2023-03-23 . |
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