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IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1002/inf2.12647
Guoyi Li, Shenghong Li, Jahangeer Ahmed, Wei Tian, Liang Li

A flexible perovskite photodetector with room-temperature self-healing function without external trigger is developed. A crosslinked polyurethane network is filled to the grain boundary of perovskite film, which not only improves the crystal quality of perovskite and mechanical stability but also enables flexible perovskite photodetectors to self-heal at room temperature.

本研究开发了一种无需外部触发即可实现室温自愈合功能的柔性包晶光电探测器。在透辉石薄膜的晶界处填充了交联聚氨酯网络,不仅提高了透辉石的晶体质量和机械稳定性,还使柔性透辉石光电探测器能够在室温下自愈合。
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引用次数: 0
Transferable, highly crystalline covellite membrane for multifunctional thermoelectric systems 用于多功能热电系统的可转移高结晶沸石膜
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-16 DOI: 10.1002/inf2.12626
Myungwoo Choi, Geonhee Lee, Yea-Lee Lee, Hyejeong Lee, Jin-Hoon Yang, Hanhwi Jang, Hyeonseok Han, MinSoung Kang, Seonggwang Yoo, A-Rang Jang, Yong Suk Oh, Inkyu Park, Min-Wook Oh, Hosun Shin, Seokwoo Jeon, Jeong-O Lee, Donghwi Cho

Emerging freestanding membrane technologies, especially using inorganic thermoelectric materials, demonstrate the potential for advanced thermoelectric platforms. However, using rare and toxic elements during material processing must be circumvented. Herein, we present a scalable method for synthesizing highly crystalline CuS membranes for thermoelectric applications. By sulfurizing crystalline Cu, we produce a highly percolated and easily transferable network of submicron CuS rods. The CuS membrane effectively separates thermal and electrical properties to achieve a power factor of 0.50 mW m−1 K−2 and thermal conductivity of 0.37 W m−1 K−1 at 650 K (estimated value). This yields a record-high dimensionless figure-of-merit of 0.91 at 650 K (estimated value) for covellite. Moreover, integrating 12 CuS devices into a module resulted in a power generation of ~4 μW at ΔT of 40 K despite using a straightforward configuration with only p-type CuS. Furthermore, based on the temperature-dependent electrical characteristics of CuS, we develop a wearable temperature sensor with antibacterial properties.

新兴的独立膜技术,尤其是使用无机热电材料的技术,展示了先进热电平台的潜力。然而,在材料加工过程中必须避免使用稀有和有毒元素。在此,我们提出了一种可扩展的方法,用于合成热电应用领域的高结晶 CuS 膜。通过对结晶铜进行硫化,我们生产出了一种高度渗透且易于转移的亚微米级 CuS 棒网络。CuS 膜有效地分离了热性能和电性能,在 650 K(估计值)时,功率因数达到 0.50 mW m-1 K-2,热导率达到 0.37 W m-1 K-1。这样,在 650 K(估计值)的条件下,科维莱特的无量纲功率因数达到了创纪录的 0.91。此外,将 12 个 CuS 器件集成到一个模块中,在 40 K 的 ΔT 温度下可产生约 4 μW 的功率,尽管使用的是仅有 p 型 CuS 的简单配置。此外,基于 CuS 随温度变化的电气特性,我们开发出了一种具有抗菌特性的可穿戴温度传感器。
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引用次数: 0
Back cover image 封底图片
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-25 DOI: 10.1002/inf2.12633
Heping Zhao, Yuewei Li, Chao Mi, Yingzhu Zi, Xue Bai, Asif Ali Haider, Yangke Cun, Anjun Huang, Yue Liu, Jianbei Qiu, Zhiguo Song, Jiayan Liao, Ji Zhou, Zhengwen Yang

A novel strategy explores the reversible modulation of visible and NIR luminescence in rare earth ion-doped photochromic bismuth-based glasses for information encryption and multi-dimensional optical storage.

一种新颖的策略探索了稀土离子掺杂的光致变色铋基玻璃中可见光和近红外发光的可逆调制,用于信息加密和多维光学存储。
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引用次数: 0
Miniature and cost-effective self-powered triboelectric sensing system toward rapid detection of puerarin concentration 用于快速检测葛根素浓度的微型、经济高效的自供电三电传感系统
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-16 DOI: 10.1002/inf2.12624
Chang Su, Jiajia Shao, Zeyang Yu, Al Mahadi Hasan, Chengmin Bao, Chris R. Bowen, Chuanbo Li, Zhong Lin Wang, Ya Yang
The detection of puerarin concentration is an essential capability to study the functional role of the Pueraria root as a natural medicine and dietary source in the treatment of cardiovascular diseases and liver protection. Current methods to detect and measure puerarin concentration, such as ultraviolet–visible spectrophotometry (UV), are bulky, require an external power supply, and are inconvenient to use. Here, we propose a triboelectric puerarin-detecting sensor (TPDS) which is based on liquid–solid contact electrification, in which liquid–solid interactions generate rapid electrical signals in only 0.4 ms to enable real-time detection of puerarin concentration in water droplets. The electrical signal of the TPDS decreases with an increase of puerarin concentration, and the sensitivity of the approach is 520 V·(μg/mL)−1. The TPDS represents a miniature and cost-effective sensor that is 0.2% of the size and 0.01% of the cost of a UV spectrophotometer. Our theoretical analysis verified that the puerarin concentration in droplets can effectively regulate the electronic structure, where higher concentrations of puerarin lead to a narrower energy bandgap, which allows the TPDS to detect puerarin concentration without the need for an external power supply. The TPDS therefore provides a route for the development of a portable and self-powered method to measure the concentration of an active ingredient in droplets through the conversion of natural energy.
检测葛根素浓度是研究葛根作为天然药物和膳食来源在治疗心血管疾病和保护肝脏方面的功能作用的一项基本能力。目前检测和测量葛根素浓度的方法,如紫外可见分光光度法(UV),体积庞大,需要外接电源,使用不便。在此,我们提出了一种基于液固接触通电的三电葛根素检测传感器(TPDS),通过液固相互作用在短短 0.4 毫秒内产生快速电信号,从而实现对水滴中葛根素浓度的实时检测。TPDS 的电信号随葛根素浓度的增加而降低,灵敏度为 520 V-(μg/mL)-1。TPDS 是一种微型且经济高效的传感器,其体积和成本仅为紫外分光光度计的 0.2%和 0.01%。我们的理论分析证实,液滴中的葛根素浓度能有效调节电子结构,葛根素浓度越高,能带隙越窄,从而使 TPDS 无需外部电源即可检测葛根素浓度。因此,TPDS 为开发一种便携式自供电方法提供了途径,这种方法可通过转换自然能量来测量液滴中活性成分的浓度。
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引用次数: 0
Continuous synthesis of metal oxide-supported high-entropy alloy nanoparticles with remarkable durability and catalytic activity in the hydrogen reduction reaction 在氢还原反应中连续合成具有显著耐久性和催化活性的金属氧化物支撑高熵合金纳米粒子
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-09 DOI: 10.1002/inf2.12617
Wail Al Zoubi, Stefano Leoni, Bassem Assfour, Abdul Wahab Allaf, Jee-Hyun Kang, Young Gun Ko
Metal oxide-supported multielement alloy nanoparticles are very promising as highly efficient and cost-effective catalysts with a virtually unlimited compositional space. However, controllable synthesis of ultrasmall multielement alloy nanoparticles (us-MEA-NPs) supported on porous metal oxides with a homogeneous elemental distribution and good catalytic stability during long-term operation is extremely challenging due to their oxidation and strong immiscibility. As a proof of concept that such synthesis can be realized, this work presents a general “bottom-up” l ultrasonic-assisted, simultaneous electro-oxidation–reduction-precipitation strategy for alloying dissimilar elements into single NPs on a porous support. One characteristic of this technique is uniform mixing, which results from simultaneous rapid thermal decomposition and reduction and leads to multielement liquid droplet solidification without aggregation. This process was achieved through a synergistic combination of enhanced electrochemical and plasma-chemical phenomena at the metal–electrolyte interface (electron energy of 0.3–1.38 eV at a peak temperature of 3000 K reached within seconds at a rate of ~105 K per second) in an aqueous solution under an ultrasonic field (40 kHz). Illustrating the effectiveness of this approach, the CuAgNiFeCoRuMn@MgO-P3000 catalyst exhibited exceptional catalytic efficiency in selective hydrogenation of nitro compounds, with over 99% chemoselectivity and nearly 100% conversion within 60 s and no decrease in catalytic activity even after 40 cycles (>98% conversion in 120 s). Our results provide an effective, transferable method for rationally designing supported MEA-NP catalysts at the atomic level and pave the way for a wide variety of catalytic reactions.
金属氧化物支撑的多元素合金纳米粒子具有无限的组成空间,是一种非常有前途的高效、经济催化剂。然而,由于多孔金属氧化物的氧化性和强不溶性,要在多孔金属氧化物上可控合成具有均匀元素分布和长期运行期间良好催化稳定性的超小型多元素合金纳米颗粒(us-MEA-NPs)极具挑战性。为了证明这种合成方法是可行的,本研究提出了一种 "自下而上 "的超声波辅助同步电氧化还原沉淀策略,用于在多孔支撑物上将异种元素合金化为单一的 NPs。该技术的一个特点是均匀混合,这源于同时进行的快速热分解和还原,并导致多元素液滴凝固而不聚集。这一过程是在超声波场(40 kHz)下的水溶液中,通过增强金属-电解质界面上的电化学和等离子体-化学现象(电子能量为 0.3-1.38 eV,峰值温度为 3000 K,在几秒钟内以每秒约 105 K 的速度达到)的协同组合实现的。为说明这种方法的有效性,CuAgNiFeCoRuMn@MgO-P3000 催化剂在硝基化合物的选择性加氢反应中表现出卓越的催化效率,化学选择性超过 99%,在 60 秒内转化率接近 100%,即使经过 40 个循环(120 秒内转化率达到 98%),催化活性也没有降低。我们的研究结果为在原子水平上合理设计支撑型 MEA-NP 催化剂提供了一种有效的、可移植的方法,并为多种催化反应铺平了道路。
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引用次数: 0
Computing imaging in shortwave infrared bands enabled by MoTe2/Si 2D-3D heterojunction-based photodiode 基于 MoTe2/Si 2D-3D 异质结的光电二极管可实现短波红外波段的计算成像
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-27 DOI: 10.1002/inf2.12618
Dongfeng Shi, Jiawang Chen, Menglei Zhu, Zijun Guo, Zixin He, Ming Li, Di Wu, Yingjian Wang, Liang Li
Breakthroughs brought about by two-dimensional (2D) materials in the field of photodetection have opened up new possibilities in infrared imaging. However, challenges still exist in fabricating high-density detector arrays using such materials, which are essential for traditional imaging systems. In this study, we present a state-of-the-art computing imaging system that utilizes a MoTe2/Si self-powered photodetector coupled with flexible Hadamard modulation algorithms. This system demonstrates remarkable capability to produce high-quality images in the shortwave infrared (SWIR) band, surpassing the capabilities of devices based on alternative material systems. The exceptional infrared imaging capability primarily stems from the MoTe2/Si photodetector's inherent features, including an ultra-wide spectral range (265–1550 nm) and extremely high sensitivity (linear dynamic range (LDR) up to 123 dB, responsivity (R) up to 0.33 A W–1, external quantum efficiency (EQE) up to 43% and a specific detectivity (D*) exceeding 2.9 × 1011 Jones). Moreover, the imaging system demonstrates the ability to achieve high-quality edge imaging of objects in the SWIR band (1550 nm), even in strong scattering environments and under low sampling rate conditions (sampling rate of 25%). We believe that this work will effectively advance the application scope of 2D materials in the field of computational imaging in SWIR bands.
二维(2D)材料在光电探测领域取得的突破为红外成像带来了新的可能性。然而,使用这种材料制造高密度探测器阵列仍然存在挑战,而这对于传统成像系统来说是必不可少的。在本研究中,我们介绍了一种最先进的计算成像系统,该系统利用 MoTe2/Si 自供电光电探测器和灵活的 Hadamard 调制算法。该系统在短波红外(SWIR)波段生成高质量图像的能力非同一般,超越了基于其他材料系统的设备。卓越的红外成像能力主要源于 MoTe2/Si 光电探测器的固有特性,包括超宽光谱范围(265-1550 nm)和极高的灵敏度(线性动态范围 (LDR) 高达 123 dB,响应率 (R) 高达 0.33 A W-1,外部量子效率 (EQE) 高达 43%,比检测率 (D*) 超过 2.9 × 1011 Jones)。此外,即使在强散射环境和低采样率条件下(采样率为 25%),该成像系统也能实现对西南红外波段(1550 nm)物体的高质量边缘成像。我们相信,这项工作将有效推进二维材料在西南红外波段计算成像领域的应用范围。
{"title":"Computing imaging in shortwave infrared bands enabled by MoTe2/Si 2D-3D heterojunction-based photodiode","authors":"Dongfeng Shi, Jiawang Chen, Menglei Zhu, Zijun Guo, Zixin He, Ming Li, Di Wu, Yingjian Wang, Liang Li","doi":"10.1002/inf2.12618","DOIUrl":"https://doi.org/10.1002/inf2.12618","url":null,"abstract":"Breakthroughs brought about by two-dimensional (2D) materials in the field of photodetection have opened up new possibilities in infrared imaging. However, challenges still exist in fabricating high-density detector arrays using such materials, which are essential for traditional imaging systems. In this study, we present a state-of-the-art computing imaging system that utilizes a MoTe<sub>2</sub>/Si self-powered photodetector coupled with flexible Hadamard modulation algorithms. This system demonstrates remarkable capability to produce high-quality images in the shortwave infrared (SWIR) band, surpassing the capabilities of devices based on alternative material systems. The exceptional infrared imaging capability primarily stems from the MoTe<sub>2</sub>/Si photodetector's inherent features, including an ultra-wide spectral range (265–1550 nm) and extremely high sensitivity (linear dynamic range (LDR) up to 123 dB, responsivity (<i>R</i>) up to 0.33 A W<sup>–1</sup>, external quantum efficiency (EQE) up to 43% and a specific detectivity (<i>D</i>*) exceeding 2.9 × 10<sup>11</sup> Jones). Moreover, the imaging system demonstrates the ability to achieve high-quality edge imaging of objects in the SWIR band (1550 nm), even in strong scattering environments and under low sampling rate conditions (sampling rate of 25%). We believe that this work will effectively advance the application scope of 2D materials in the field of computational imaging in SWIR bands.","PeriodicalId":48538,"journal":{"name":"Infomat","volume":"27 1","pages":""},"PeriodicalIF":22.7,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142224424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bifunctional self-segregated electrolyte realizing high-performance zinc-iodine batteries 实现高性能锌碘电池的双功能自分离电解质
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-27 DOI: 10.1002/inf2.12620
Xueting Hu, Zequan Zhao, Yongqiang Yang, Hao Zhang, Guojun Lai, Bingan Lu, Peng Zhou, Lina Chen, Jiang Zhou
Static rechargeable zinc-iodine (Zn-I2) batteries are superior in safety, cost-effectiveness, and sustainability, giving them great potential for large-scale energy storage applications. However, the shuttle effect of polyiodides on the cathode and the unstable anode/electrolyte interface hinder the development of Zn-I2 batteries. Herein, a self-segregated biphasic electrolyte (SSBE) was proposed to synergistically address those issues. The strong interaction between polyiodides and the organic phase was demonstrated to limit the shuttle effect of polyiodides. Meanwhile, the hybridization of polar organic solvent in the inorganic phase modulated the bonding structure, as well as the effective weakening of water activity, optimizing the interface during zinc electroplating. As a result, the Zn-I2 coin cells performed a capacity retention of nearly 100% after 4000 cycles at 2 mA cm−2. And a discharge capacity of 0.6 Ah with no degradation after 180 cycles was achieved in the pouch cell. A photovoltaic energy storage battery was further achieved and displayed a cumulative capacity of 5.85 Ah. The successfully designed energy storage device exhibits the application potential of Zn-I2 batteries for stationary energy storage.
静态可充电锌碘电池(Zn-I2)在安全性、成本效益和可持续性方面都具有优势,因此在大规模储能应用方面具有巨大潜力。然而,多碘化物在阴极上的穿梭效应和不稳定的阳极/电解质界面阻碍了锌碘电池的发展。在此,我们提出了一种自分离双相电解质(SSBE)来协同解决这些问题。研究证明,聚碘化物与有机相之间的强相互作用限制了聚碘化物的穿梭效应。同时,无机相中极性有机溶剂的杂化调节了键合结构,并有效削弱了水活性,优化了锌电镀过程中的界面。因此,Zn-I2 纽扣电池在 2 mA cm-2 下循环 4000 次后,容量保持率接近 100%。在袋式电池中,经过 180 次循环后,放电容量达到 0.6 Ah,且无衰减。进一步实现了光伏储能电池,并显示出 5.85 Ah 的累积容量。设计成功的储能装置展示了 Zn-I2 电池在固定储能方面的应用潜力。
{"title":"Bifunctional self-segregated electrolyte realizing high-performance zinc-iodine batteries","authors":"Xueting Hu, Zequan Zhao, Yongqiang Yang, Hao Zhang, Guojun Lai, Bingan Lu, Peng Zhou, Lina Chen, Jiang Zhou","doi":"10.1002/inf2.12620","DOIUrl":"https://doi.org/10.1002/inf2.12620","url":null,"abstract":"Static rechargeable zinc-iodine (Zn-I<sub>2</sub>) batteries are superior in safety, cost-effectiveness, and sustainability, giving them great potential for large-scale energy storage applications. However, the shuttle effect of polyiodides on the cathode and the unstable anode/electrolyte interface hinder the development of Zn-I<sub>2</sub> batteries. Herein, a self-segregated biphasic electrolyte (SSBE) was proposed to synergistically address those issues. The strong interaction between polyiodides and the organic phase was demonstrated to limit the shuttle effect of polyiodides. Meanwhile, the hybridization of polar organic solvent in the inorganic phase modulated the bonding structure, as well as the effective weakening of water activity, optimizing the interface during zinc electroplating. As a result, the Zn-I<sub>2</sub> coin cells performed a capacity retention of nearly 100% after 4000 cycles at 2 mA cm<sup>−2</sup>. And a discharge capacity of 0.6 Ah with no degradation after 180 cycles was achieved in the pouch cell. A photovoltaic energy storage battery was further achieved and displayed a cumulative capacity of 5.85 Ah. The successfully designed energy storage device exhibits the application potential of Zn-I<sub>2</sub> batteries for stationary energy storage.","PeriodicalId":48538,"journal":{"name":"Infomat","volume":"27 1","pages":""},"PeriodicalIF":22.7,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142224422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Back cover image 封底图片
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-21 DOI: 10.1002/inf2.12622
Qiang Wang, Yachuan Wang, Yankun Wang, Luyue Jiang, Jinyan Zhao, Zhitang Song, Jinshun Bi, Libo Zhao, Zhuangde Jiang, Jutta Schwarzkopf, Shengli Wu, Bin Zhang, Wei Ren, Sannian Song, Gang Niu

Hardware neuromorphic computing based on phase-change random access memories brings about a spring of artificial intelligence.

基于相变随机存取存储器的硬件神经形态计算带来了人工智能的春天。
{"title":"Back cover image","authors":"Qiang Wang,&nbsp;Yachuan Wang,&nbsp;Yankun Wang,&nbsp;Luyue Jiang,&nbsp;Jinyan Zhao,&nbsp;Zhitang Song,&nbsp;Jinshun Bi,&nbsp;Libo Zhao,&nbsp;Zhuangde Jiang,&nbsp;Jutta Schwarzkopf,&nbsp;Shengli Wu,&nbsp;Bin Zhang,&nbsp;Wei Ren,&nbsp;Sannian Song,&nbsp;Gang Niu","doi":"10.1002/inf2.12622","DOIUrl":"https://doi.org/10.1002/inf2.12622","url":null,"abstract":"<p>Hardware neuromorphic computing based on phase-change random access memories brings about a spring of artificial intelligence.\u0000\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":48538,"journal":{"name":"Infomat","volume":"6 8","pages":""},"PeriodicalIF":22.7,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/inf2.12622","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142041642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Promoting uniform lithium deposition with Janus gel polymer electrolytes enabling stable lithium metal batteries 利用 Janus 凝胶聚合物电解质促进锂的均匀沉积,实现稳定的锂金属电池
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-14 DOI: 10.1002/inf2.12551
Lin Wang, Shugang Xu, Zihui Song, Wanyuan Jiang, Shouhai Zhang, Xigao Jian, Fangyuan Hu

Lithium metal batteries (LMBs) are desirable candidates owing to their high-energy advantage for next-generation batteries. However, the practical application of LMBs continues to be constrained by thorny safety issues with the formation and growth of Li dendrites. Herein, the ZIF-67 MOFs are in situ coupled onto a single face of 3D porous nanofiber to fabricate an asymmetric Janus membrane, harnessing their anion adsorption capabilities to promote the uniform deposition of Li ions. In addition, the poly(ethylene glycol) diacrylate and trifluoromethyl methacrylate are introduced into nanofiber skeleton to form Janus@GPE, which preferentially reacts with Li metal to form a LiF-rich stable SEI layer to inhibit Li dendrite growth. Importantly, the synergistic effect of the MOFs and stable solid electrolyte interphase (SEI) layer results in superior cycling performance, achieving a remarkable 2500 h cycling at 1 mA cm−2 in the Li/Janus@GPE/Li configuration. In addition, the Janus@GPE electrolyte has a certain flame retardant, which can self-extinguish within 3 s, improving the safety performance of the batteries. Consequently, the Li/Janus@GPE/LFP flexible pouch cell exhibits favorable cycling stability (the capacity retention rate of 45 cycles is 91.8% at 0.1 C). This work provides new insights and strategies to improve the safety and practical utility of LMBs.

锂金属电池(LMB)具有高能量优势,是下一代电池的理想候选材料。然而,LMB 的实际应用仍然受到锂枝晶形成和生长的棘手安全问题的制约。在本文中,ZIF-67 MOFs 被原位耦合到三维多孔纳米纤维的单面上,制成了非对称 Janus 膜,利用其阴离子吸附能力促进锂离子的均匀沉积。此外,在纳米纤维骨架中引入聚乙二醇二丙烯酸酯和甲基丙烯酸三氟甲基酯,形成 Janus@GPE,优先与金属锂反应,形成富含 LiF 的稳定 SEI 层,抑制锂枝晶的生长。重要的是,MOFs 和稳定的固体电解质相(SEI)层的协同效应带来了卓越的循环性能,在锂/Janus@GPE/锂配置中,1 mA cm-2 的循环时间达到了 2500 h。此外,Janus@GPE 电解质具有一定的阻燃性,可在 3 秒内自熄,提高了电池的安全性能。因此,锂/Janus@GPE/LFP 柔性袋电池表现出良好的循环稳定性(在 0.1 C 下,45 次循环的容量保持率为 91.8%)。这项工作为提高锂电池的安全性和实用性提供了新的见解和策略。
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引用次数: 0
Rational composition engineering for high-quality Pb–Sn photodetector toward sensitive near-infrared digital imaging arrays 面向灵敏近红外数字成像阵列的高质量铅锑光电探测器的合理成分工程设计
IF 22.7 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-13 DOI: 10.1002/inf2.12615
Huan Li, Yu Gao, Xin Hong, Kanghui Ke, Zilong Ye, Siwei Zhang, Kefei Shi, Zhuo Peng, Hao Yan, Man-Chung Tang, Youwei Yao, Ben Zhong Tang, Guodan Wei, Feiyu Kang
Broadband photodetectors (PDs) capable of multi-wavelength detection have garnered significant interest for applications in environmental monitoring, optical communication, spectral analysis, and imaging sensing. Low-bandgap Pb–Sn hybrid perovskite photodetectors can extend the spectral response from the ultraviolet–visible (UV–vis) range to the near-infrared (NIR) and reduce the toxicity associated with Pb2+. The strategic introduction of Sn2+ into Cs0.15FA0.85PbxSn1−xI3 (x = 1, 0.8, 0.6, 0.5, 0.4, 0.2, and 0) not only preserves the cubic crystal structure with conformal multigrain growth but also broadens the film's absorption spectrum from 800 to 1000 nm NIR region. This indicates a well-controlled tunability of the Pb–Sn binary perovskite system. Specifically, the self-powered photodetector with a device structure of ITO/NiOx/PTAA/Cs0.15FA0.85Pb0.5Sn0.5I3/PCBM/BCP/Ag has shown remarkable optoelectrical properties. It exhibits a high external quantum efficiency (EQE) of up to 80% across the spectrum from 300 to 1000 nm, a responsivity (R) exceeding 0.5 A/W, and high detectivity (D*) value of 1.04 × 1012 Jones at 910 nm and 3.38 × 1011 Jones at 1000 nm after weak attenuation. Intriguingly, the dark current of the Cs0.15FA0.85Pb0.5Sn0.5I3 device is four orders of magnitude lower than that of devices made with pristine Pb or Sn only, strongly correlating with its significantly increased built-in potential and reduced trap density. Consequently, it demonstrates a −3 dB bandwidth of 2.23 × 104 Hz, fast rise and decay times of 61 and 30 μs, respectively, and a linear dynamic range (LDR) of 155 dB. Benefiting from its high sensitivity, a 5 × 5 PD array for NIR imaging and non-invasive pulse detection for photoplethysmography applications has been successfully demonstrated, showcasing the prosperous potential of Pb–Sn hybrid perovskite in the NIR range.
能够进行多波长检测的宽带光电探测器(PD)在环境监测、光通信、光谱分析和成像传感等领域的应用引起了人们的极大兴趣。低带隙铅锡混合包晶光电探测器可将光谱响应从紫外-可见(UV-vis)范围扩展到近红外(NIR),并降低与 Pb2+ 相关的毒性。在 Cs0.15FA0.85PbxSn1-xI3(x = 1、0.8、0.6、0.5、0.4、0.2 和 0)中战略性地引入 Sn2+,不仅保留了保形多晶粒生长的立方晶体结构,还拓宽了薄膜在 800 纳米到 1000 纳米近红外区域的吸收光谱。这表明铅锑二元包晶体系具有良好的可调谐性。具体来说,ITO/NiOx/PTAA/Cs0.15FA0.85Pb0.5Sn0.5I3/PCBM/BCP/Ag 器件结构的自供电光电探测器显示出显著的光电特性。它在 300 纳米到 1000 纳米的光谱范围内表现出高达 80% 的外部量子效率 (EQE)、超过 0.5 A/W 的响应度 (R),以及在 910 纳米和 1000 纳米微弱衰减后分别达到 1.04 × 1012 琼斯和 3.38 × 1011 琼斯的高探测度 (D*)。耐人寻味的是,Cs0.15FA0.85Pb0.5Sn0.5I3 器件的暗电流比仅使用纯铅或纯锡制造的器件低四个数量级,这与它显著提高的内置电势和降低的陷阱密度密切相关。因此,它的 -3 dB 带宽为 2.23 × 104 Hz,快速上升和衰减时间分别为 61 和 30 μs,线性动态范围 (LDR) 为 155 dB。得益于其高灵敏度,一个用于近红外成像和无创脉冲检测的 5 × 5 光致发光阵列已被成功演示,用于光心动图应用,展示了铅锡混合包晶在近红外范围的巨大潜力。
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引用次数: 0
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