首页 > 最新文献

SmartMat最新文献

英文 中文
Compacted mesoporous titania nanosheets anode for pseudocapacitance‐dominated, high‐rate, and high‐volumetric sodium‐ion storage 紧凑的介孔二氧化钛纳米片阳极用于假电容主导,高速率和高容量的钠离子存储
Pub Date : 2023-03-10 DOI: 10.1002/smm2.1192
Jiayu Yu, Xiaojuan Huang, Yalin He, Dafu Tang, Ting Huang, Lu Liu, Haobin Wu, D. Peng, Dongyuan Zhao, Kun Lan, Qiulong Wei
Surface‐redox pseudocapacitive nanomaterials show promise for fast‐charging energy storage. However, their high surface area usually leads to low density, which is not conducive to achieving both high volumetric capacity and high‐rate capability. Herein, we demonstrate that TiO2 nanosheets (meso‐TiO2‐NSs) with densely packed mesoporous are capable of fast pseudocapacitance‐dominated sodium‐ion storage, as well as high volumetric and gravimetric capacities. Through compressing treatment, the compaction density of meso‐TiO2‐NSs is up to ~1.6 g/cm3, combined with high surface area and high porosity with mesopore channels for rapid Na+ diffusion. The compacted meso‐TiO2‐NSs electrodes achieve high pseudocapacitance (93.6% of total charge at 1 mV/s), high‐rate capability (up to 10 A/g), and long‐term cycling stability (10,000 cycles). More importantly, the space‐efficiently packed structure enables high volumetric capacity. The thick‐film meso‐TiO2‐NSs anode with the mass loading of 10 mg/cm2 delivers a gravimetric capacity of 165 mAh/g and a volumetric capacity of 223 mAh/cm3 at 5 mA/cm2, much higher than those of commercial hard carbon anode (80 mAh/g and 86 mAh/cm3). This work highlights a pathway for designing a dense nanostructure that enables fast charge kinetics for high‐density sodium‐ion storage.
表面氧化还原赝电容纳米材料显示出快速充电储能的前景。然而,它们的高表面积通常导致低密度,这不利于实现高容量和高速率的能力。在此,我们证明了密集排列的介孔TiO2纳米片(meso - TiO2 - NSs)能够快速存储假电容主导的钠离子,以及高容量和重量容量。通过压缩处理,meso - TiO2 - NSs的压实密度可达~1.6 g/cm3,具有高表面积和高孔隙率的介孔通道,有利于Na+的快速扩散。紧凑的介观- TiO2 - NSs电极具有高赝电容(1mv /s时总电荷的93.6%),高速率容量(高达10a /g)和长期循环稳定性(10,000次循环)。更重要的是,高效的空间填充结构实现了高容量。质量负载为10 mg/cm2的厚膜介膜TiO2 - NSs阳极的重量容量为165 mAh/g, 5 mA/cm2时的体积容量为223 mAh/cm3,远高于商用硬碳阳极(80 mAh/g和86 mAh/cm3)。这项工作强调了设计致密纳米结构的途径,该结构可以实现高密度钠离子存储的快速充电动力学。
{"title":"Compacted mesoporous titania nanosheets anode for pseudocapacitance‐dominated, high‐rate, and high‐volumetric sodium‐ion storage","authors":"Jiayu Yu, Xiaojuan Huang, Yalin He, Dafu Tang, Ting Huang, Lu Liu, Haobin Wu, D. Peng, Dongyuan Zhao, Kun Lan, Qiulong Wei","doi":"10.1002/smm2.1192","DOIUrl":"https://doi.org/10.1002/smm2.1192","url":null,"abstract":"Surface‐redox pseudocapacitive nanomaterials show promise for fast‐charging energy storage. However, their high surface area usually leads to low density, which is not conducive to achieving both high volumetric capacity and high‐rate capability. Herein, we demonstrate that TiO2 nanosheets (meso‐TiO2‐NSs) with densely packed mesoporous are capable of fast pseudocapacitance‐dominated sodium‐ion storage, as well as high volumetric and gravimetric capacities. Through compressing treatment, the compaction density of meso‐TiO2‐NSs is up to ~1.6 g/cm3, combined with high surface area and high porosity with mesopore channels for rapid Na+ diffusion. The compacted meso‐TiO2‐NSs electrodes achieve high pseudocapacitance (93.6% of total charge at 1 mV/s), high‐rate capability (up to 10 A/g), and long‐term cycling stability (10,000 cycles). More importantly, the space‐efficiently packed structure enables high volumetric capacity. The thick‐film meso‐TiO2‐NSs anode with the mass loading of 10 mg/cm2 delivers a gravimetric capacity of 165 mAh/g and a volumetric capacity of 223 mAh/cm3 at 5 mA/cm2, much higher than those of commercial hard carbon anode (80 mAh/g and 86 mAh/cm3). This work highlights a pathway for designing a dense nanostructure that enables fast charge kinetics for high‐density sodium‐ion storage.","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83529503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Rebirth of CuInS 2 as hole transport material for perovskite solar cells 钙钛矿太阳能电池空穴输运材料CuInS 2的再生
Pub Date : 2023-03-10 DOI: 10.1002/smm2.1195
R. Ahmed
{"title":"Rebirth of CuInS\u0000 2\u0000 as hole transport material for perovskite solar cells","authors":"R. Ahmed","doi":"10.1002/smm2.1195","DOIUrl":"https://doi.org/10.1002/smm2.1195","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79891116","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Materials and structural design for preferable Zn deposition behavior toward stable Zn anodes 制备稳定锌阳极的材料及结构设计
Pub Date : 2023-03-08 DOI: 10.1002/smm2.1194
Qinghe Cao, Yong Gao, Jie Pu, Abdelnaby M. Elshahawy, C. Guan
{"title":"Materials and structural design for preferable Zn deposition behavior toward stable Zn anodes","authors":"Qinghe Cao, Yong Gao, Jie Pu, Abdelnaby M. Elshahawy, C. Guan","doi":"10.1002/smm2.1194","DOIUrl":"https://doi.org/10.1002/smm2.1194","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74842191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Single‐precursor phase‐controlled synthesis of copper selenide nanocrystals and their conversion to amorphous hollow nanostructures 单前驱体控制的硒化铜纳米晶的合成及其向非晶中空纳米结构的转化
Pub Date : 2023-03-03 DOI: 10.1002/smm2.1193
Feifan Chen, Yadong Zhang, Lijun Hu, Lifang Zheng, Feiyue Ge, Changsheng Feng, Dan-tong Xu, Ch Tao, Xuejun Wu
The crystal phases are essential to the physicochemical properties and functionalities of materials. Copper selenide has emerged as an important and appealing semiconductor, which can exist in a variety of polymorphic phases. However, the richness of polymorphs also makes it a challenge to the direct preparation of copper selenide nanocrystals with tunable phases. Herein, two polymorphs, that is, quasi‐tetragonal Cu2−xSe nanocubes and metastable wurtzite Cu2Se nanodisks, are successfully synthesized by using a single precursor, copper(I) selenocyanate (CuSeCN), as the Cu and Se sources. The key to phase modulation is the optimal choice of the ligand in the synthesis. The as‐prepared nanocrystals possess different morphologies and compositions, giving rise to distinct optical properties and electrical conductivities. Interestingly, the copper selenide nanocrystals can provide a platform for the rational construction of two types of amorphous hollow Au─Cu─Se nanostructures by reaction with Au(I) precursor, in which their final shapes are well kept as that of the original nanocrystal templates. This work provides an easy strategy for the phase‐controlled synthesis of copper selenide nanocrystals and enables the design of new materials for broad applications.
晶体相对材料的物理化学性质和功能至关重要。硒化铜是一种重要的、具有吸引力的半导体,它可以存在于多种多晶相中。然而,多晶的丰富性也给直接制备具有可调相的硒化铜纳米晶体带来了挑战。本文以硒酸铜(Cu)和硒酸铜(CuSeCN)为前驱体,成功合成了准四方Cu2−xSe纳米立方体和亚稳纤锌矿Cu2Se纳米圆盘。相位调制的关键是合成过程中配体的最佳选择。制备的纳米晶体具有不同的形貌和组成,产生不同的光学性质和电导率。有趣的是,硒化铜纳米晶体可以通过与Au(I)前驱体反应,为合理构建两种非晶空心Au─Cu─Se纳米结构提供平台,其最终形状与原始纳米晶体模板保持一致。这项工作为相控合成硒化铜纳米晶体提供了一种简单的策略,并使新材料的设计具有广泛的应用前景。
{"title":"Single‐precursor phase‐controlled synthesis of copper selenide nanocrystals and their conversion to amorphous hollow nanostructures","authors":"Feifan Chen, Yadong Zhang, Lijun Hu, Lifang Zheng, Feiyue Ge, Changsheng Feng, Dan-tong Xu, Ch Tao, Xuejun Wu","doi":"10.1002/smm2.1193","DOIUrl":"https://doi.org/10.1002/smm2.1193","url":null,"abstract":"The crystal phases are essential to the physicochemical properties and functionalities of materials. Copper selenide has emerged as an important and appealing semiconductor, which can exist in a variety of polymorphic phases. However, the richness of polymorphs also makes it a challenge to the direct preparation of copper selenide nanocrystals with tunable phases. Herein, two polymorphs, that is, quasi‐tetragonal Cu2−xSe nanocubes and metastable wurtzite Cu2Se nanodisks, are successfully synthesized by using a single precursor, copper(I) selenocyanate (CuSeCN), as the Cu and Se sources. The key to phase modulation is the optimal choice of the ligand in the synthesis. The as‐prepared nanocrystals possess different morphologies and compositions, giving rise to distinct optical properties and electrical conductivities. Interestingly, the copper selenide nanocrystals can provide a platform for the rational construction of two types of amorphous hollow Au─Cu─Se nanostructures by reaction with Au(I) precursor, in which their final shapes are well kept as that of the original nanocrystal templates. This work provides an easy strategy for the phase‐controlled synthesis of copper selenide nanocrystals and enables the design of new materials for broad applications.","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90178061","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
High‐power and low‐cost sodium‐ion batteries with a wide operation temperature from −70 °C to 130 °C 高功率和低成本的钠离子电池,工作温度从- 70°C到130°C
Pub Date : 2023-02-27 DOI: 10.1002/smm2.1191
Zhi Li, Yu Zhang, Yonggang Wang
Low‐cost sodium‐ion batteries (SIBs) are promising candidates for grid‐scale energy‐storage systems, and the wide‐temperature operations of SIBs are highly demanded to accommodate extreme weather. Herein, a low‐cost SIB is fabricated with a Na4Fe3(PO4)2P2O7 (NFPP) cathode, a natural graphite (NG) anode, and an ether‐based electrolyte. The prepared NG//NFPP batteries deliver a long lifespan of 1000 cycles, high‐power density of 5938 W/kg, and remarkable rate performance of 10 A/g with a high capacity retention of 60%. Benefiting from the solvent co‐intercalation process of the NG anode and the high Na+ diffusion rate of the NFPP cathode, the NG//NFPP battery displays outstanding performance at −40 °C and even can work at an ultralow temperature of −70 °C. Furthermore, the high boiling point of the electrolytes and high thermal stability of the electrode materials also enable the high‐temperature operation of the full battery up to 130 °C. This work will guide the design of the wide‐temperature SIBs.
低成本钠离子电池(sib)是电网规模储能系统的有前途的候选者,并且sib的宽温度运行被高度要求以适应极端天气。本文采用Na4Fe3(PO4)2P2O7 (NFPP)阴极、天然石墨(NG)阳极和醚基电解质制备了低成本SIB。制备的NG//NFPP电池具有1000次循环的长寿命,5938 W/kg的高功率密度,10 a /g的卓越倍率性能和60%的高容量保留率。得益于NG阳极的溶剂共插过程和NFPP阴极的高Na+扩散速率,NG//NFPP电池在- 40°C下表现出优异的性能,甚至可以在- 70°C的超低温下工作。此外,电解质的高沸点和电极材料的高热稳定性也使全电池的高温运行达到130°C。这项工作将指导宽温度sib的设计。
{"title":"High‐power and low‐cost sodium‐ion batteries with a wide operation temperature from −70 °C to 130 °C","authors":"Zhi Li, Yu Zhang, Yonggang Wang","doi":"10.1002/smm2.1191","DOIUrl":"https://doi.org/10.1002/smm2.1191","url":null,"abstract":"Low‐cost sodium‐ion batteries (SIBs) are promising candidates for grid‐scale energy‐storage systems, and the wide‐temperature operations of SIBs are highly demanded to accommodate extreme weather. Herein, a low‐cost SIB is fabricated with a Na4Fe3(PO4)2P2O7 (NFPP) cathode, a natural graphite (NG) anode, and an ether‐based electrolyte. The prepared NG//NFPP batteries deliver a long lifespan of 1000 cycles, high‐power density of 5938 W/kg, and remarkable rate performance of 10 A/g with a high capacity retention of 60%. Benefiting from the solvent co‐intercalation process of the NG anode and the high Na+ diffusion rate of the NFPP cathode, the NG//NFPP battery displays outstanding performance at −40 °C and even can work at an ultralow temperature of −70 °C. Furthermore, the high boiling point of the electrolytes and high thermal stability of the electrode materials also enable the high‐temperature operation of the full battery up to 130 °C. This work will guide the design of the wide‐temperature SIBs.","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77114809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synergistic fluorescent hydrogel actuators with selective spatial shape/color‐changing behaviors via interfacial supramolecular assembly 通过界面超分子组装具有选择性空间形状/颜色变化行为的协同荧光水凝胶致动器
Pub Date : 2023-02-24 DOI: 10.1002/smm2.1190
Wei Lu, Ruijia Wang, Muqing Si, Yi Zhang, Shuangshuang Wu, Ning Zhu, Wenqin Wang, Tao Chen
{"title":"Synergistic fluorescent hydrogel actuators with selective spatial shape/color‐changing behaviors via interfacial supramolecular assembly","authors":"Wei Lu, Ruijia Wang, Muqing Si, Yi Zhang, Shuangshuang Wu, Ning Zhu, Wenqin Wang, Tao Chen","doi":"10.1002/smm2.1190","DOIUrl":"https://doi.org/10.1002/smm2.1190","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87841637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rapid laser synthesis of surfactantless tantalum‐based nanomaterials as bifunctional catalysts for direct peroxide–peroxide fuel cells 激光快速合成无表面活性剂钽基纳米材料作为直接过氧化氢燃料电池的双功能催化剂
Pub Date : 2023-02-24 DOI: 10.1002/smm2.1181
X. Mo, Brigitte Bouchet Fabre, N. Herlin‐Boime, Edmund C. M. Tse
{"title":"Rapid laser synthesis of surfactantless tantalum‐based nanomaterials as bifunctional catalysts for direct peroxide–peroxide fuel cells","authors":"X. Mo, Brigitte Bouchet Fabre, N. Herlin‐Boime, Edmund C. M. Tse","doi":"10.1002/smm2.1181","DOIUrl":"https://doi.org/10.1002/smm2.1181","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91529376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recent developments in artificial spider silk and functional gel fibers 人造蜘蛛丝和功能性凝胶纤维的最新进展
Pub Date : 2023-02-24 DOI: 10.1002/smm2.1189
Abdul Qadeer Khan, Muhammad Shafiq, Jiatian Li, Kaiqing Yu, Zunfeng Liu, Xiang Zhou, Meifang Zhu
{"title":"Recent developments in artificial spider silk and functional gel fibers","authors":"Abdul Qadeer Khan, Muhammad Shafiq, Jiatian Li, Kaiqing Yu, Zunfeng Liu, Xiang Zhou, Meifang Zhu","doi":"10.1002/smm2.1189","DOIUrl":"https://doi.org/10.1002/smm2.1189","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73851803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Dynamic polymeric materials based on reversible B–O bonds with dative boron–nitrogen coordination 基于硼氮配位可逆B-O键的动态高分子材料
Pub Date : 2023-02-21 DOI: 10.1002/smm2.1187
Zi‐Han Zhao, Cheng‐Hui Li, J. Zuo
To minimize the environmental pollution caused by polymeric waste, materials based dynamic chemistry have attracted extensive attention around the world. Various dynamic covalent bonds or noncovalent interactions have been employed to design multifunctional polymers with recyclability, reprocessablility, and sustainability. Among them, polymers based on reversible boron–oxygen (B–O) bonds have been widely investigated because of their unique properties. Particularly, lots of scientists have demonstrated that the combination with boron–nitrogen (B–N) coordination can effectively accelerate the dynamicity as well as enhance the stability of B–O bonds. Therefore, numerous polymers containing dynamic B–O bonds with dative B–N coordination have been designed and synthesized in recent years. These polymers exhibit excellent versatility and great potential for diverse applications such as biosensors, battery electrolytes, and artificial skins. This review provides an overview of the comprehensive influence of dynamic B–N coordination chemistry on B–O bonds in organoboron species and highlights the developments in the area of constructing boron‐containing polymeric materials with this interesting linkage. The design guidelines, existing challenges, and future perspectives in this burgeoning field are discussed and proposed.
为了最大限度地减少聚合物废弃物对环境的污染,基于材料的动态化学受到了世界各国的广泛关注。各种动态共价键或非共价相互作用已被用于设计多功能聚合物的可回收性,可再加工性和可持续性。其中,基于可逆硼氧键(B-O)的聚合物因其独特的性质而受到广泛的研究。特别是,许多科学家已经证明,与硼氮(B-N)配位结合可以有效地加速动力学并增强B-O键的稳定性。因此,近年来人们设计和合成了许多含有动态B-O键和共轭B-N配位的聚合物。这些聚合物在生物传感器、电池电解质和人造皮肤等各种应用中表现出优异的多功能性和巨大的潜力。本文综述了动态B-N配位化学对有机硼中B-O键的综合影响,并重点介绍了用这种有趣的键构建含硼聚合物材料领域的进展。讨论并提出了这一新兴领域的设计指南、现有挑战和未来展望。
{"title":"Dynamic polymeric materials based on reversible B–O bonds with dative boron–nitrogen coordination","authors":"Zi‐Han Zhao, Cheng‐Hui Li, J. Zuo","doi":"10.1002/smm2.1187","DOIUrl":"https://doi.org/10.1002/smm2.1187","url":null,"abstract":"To minimize the environmental pollution caused by polymeric waste, materials based dynamic chemistry have attracted extensive attention around the world. Various dynamic covalent bonds or noncovalent interactions have been employed to design multifunctional polymers with recyclability, reprocessablility, and sustainability. Among them, polymers based on reversible boron–oxygen (B–O) bonds have been widely investigated because of their unique properties. Particularly, lots of scientists have demonstrated that the combination with boron–nitrogen (B–N) coordination can effectively accelerate the dynamicity as well as enhance the stability of B–O bonds. Therefore, numerous polymers containing dynamic B–O bonds with dative B–N coordination have been designed and synthesized in recent years. These polymers exhibit excellent versatility and great potential for diverse applications such as biosensors, battery electrolytes, and artificial skins. This review provides an overview of the comprehensive influence of dynamic B–N coordination chemistry on B–O bonds in organoboron species and highlights the developments in the area of constructing boron‐containing polymeric materials with this interesting linkage. The design guidelines, existing challenges, and future perspectives in this burgeoning field are discussed and proposed.","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82393696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A Van der Waals plug‐and‐probe approach 一种范德华塞-探针方法
Pub Date : 2023-02-21 DOI: 10.1002/smm2.1180
Tiantian Zhou, Deyang Ji
{"title":"A Van der Waals plug‐and‐probe approach","authors":"Tiantian Zhou, Deyang Ji","doi":"10.1002/smm2.1180","DOIUrl":"https://doi.org/10.1002/smm2.1180","url":null,"abstract":"","PeriodicalId":21794,"journal":{"name":"SmartMat","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85180937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
SmartMat
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1