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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 ：
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 ：
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 ：
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 ：
Windows play significant roles in today's buildings, allowing outside view and providing occupants with daylight. However, windows are also often considered to be one of the weakest building components with respect to high thermal losses, and therefore significant energy consumption is required to maintain a comfortable indoor environment. In comparison to traditional windows, dual-band electrochromic smart windows have the ability to independently regulate the transmittance of visible and near-infrared light, which will contribute to the optimal energy efficiency of building heating, cooling and artificial lighting systems. In this review, the basic concept, device structure, working principle and key factors affecting energy saving of dual-band electrochromism are briefly introduced. Next, recent advances in dual-band electrochromic materials including inorganic, organic, and composite materials are summarized in detail, with emphasis on device fabrication and applications in building energy conservation. Finally, some challenges and prospects of dual band electrochromic smart windows are introduced. It is anticipated that this review will provide new insights into the development of high-performance dual-band electrochromic smart windows toward applications in the green buildings.
Keyword ：
Energy conservation Energy conservation Green building Green building Spectral selective modulation Spectral selective modulation Dual -band electrochromism Dual -band electrochromism Smart windows Smart windows
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| GB/T 7714 | Bai, Ting , Li, Wanzhong , Fu, Guoxing et al. Dual-band electrochromic smart windows towards building energy conservation [J]. | SOLAR ENERGY MATERIALS AND SOLAR CELLS , 2023 , 256 . |
| MLA | Bai, Ting et al. "Dual-band electrochromic smart windows towards building energy conservation" . | SOLAR ENERGY MATERIALS AND SOLAR CELLS 256 (2023) . |
| APA | Bai, Ting , Li, Wanzhong , Fu, Guoxing , Zhang, Qianqian , Zhou, Kailing , Wang, Hao . Dual-band electrochromic smart windows towards building energy conservation . | SOLAR ENERGY MATERIALS AND SOLAR CELLS , 2023 , 256 . |
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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 ：
The interfacial engineering provides an effective strategy to develop the noble-free catalysts. However, the long protons migration path and undesirable electrons transportation resistance at the heterointerfaces has hampered advances in highly efficient acidic hydrogen production. Herein, the self-tuned interfacial charges in NiP/HxWO3 binary catalyst are developed for the efficiently acidic water electrocatalysis. Specifically, the interfacial electrons could be automatically tuned and accelerated by a self-modulated work function via the in-situ protonation process of WO3 from the semi-conductor to metallic tungsten bronze (HxWO3) in acidic medium. Moreover, the charge redistribution in NiP/HxWO3 balances the electronic state between surficial Ni sites and P sites, bidirectionally optimizing the hydrogen binding energy over surficial NiP for the favorable H* adsorption and H-2 release. A further promotion is achieved by constructing NiP/HxWO3 on carbon fiber fabric to form a hierarchically and seamlessly conductive nanostructure. Impressively, the interfacial charge coordinated NiP/HxWO3 catalyst exhibits outstanding HER activity with an overpotential of 280 mV at the high current density of 500 mA.cm(-2) and an excellent long-term stability beyond 110 h in acidic medium, surpassing the most reported catalysts. This work demonstrates an protonation assisted interfacial charge regulation strategy for the development of the efficient multicomponent catalyst.
Keyword ：
Self-tuned Self-tuned Interfacial charges Interfacial charges Protonation Protonation Acidic hydrogen production Acidic hydrogen production
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| GB/T 7714 | Zeng, Chuitao , Zhang, Jianhua , Xia, Lingzhi et al. Self-tuned interfacial charges induced by protonated transition metal heterostructure for efficiently acidic hydrogen evolution reaction [J]. | CHEMICAL ENGINEERING JOURNAL , 2023 , 476 . |
| MLA | Zeng, Chuitao et al. "Self-tuned interfacial charges induced by protonated transition metal heterostructure for efficiently acidic hydrogen evolution reaction" . | CHEMICAL ENGINEERING JOURNAL 476 (2023) . |
| APA | Zeng, Chuitao , Zhang, Jianhua , Xia, Lingzhi , Zhou, Kai-Ling , Jin, Yuhong , Zhang, Yongzheng et al. Self-tuned interfacial charges induced by protonated transition metal heterostructure for efficiently acidic hydrogen evolution reaction . | CHEMICAL ENGINEERING JOURNAL , 2023 , 476 . |
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