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Molecular Structure Tailoring of Organic Spacers for High‑Performance Ruddlesden–Popper Perovskite Solar Cells

Nano-Micro Letters 2025年第2期17卷 314-357页

作者： Pengyun Liu Xuejin Li Tonghui Cai Wei Xing Naitao Yang Hamidreza Arandiyan Zongping Shao Shaobin Wang Shaomin Liu School of materials science and engineering State Key Laboratory of Heavy Oil ProcessingChina University of Petroleum(East China)Qingdao 266580People’s Republic of China School of Chemistry and Chemical engineering Shandong University of TechnologyZibo 255049People’s Republic of China Centre for Applied materials and Industrial Chemistry(CAMIC) School of ScienceRMIT UniversityMelbourneVic 3000Australia WA School of Mines:Minerals Energy and Chemical Engineering(WASM‑MECE)Curtin UniversityPerthWA 6102Australia School of Chemical engineering The University of AdelaideAdelaideSA 5005Australia School of engineering Great Bay UniversityDongguan 523000People’s Republic of China

Layer-structured Ruddlesden–Popper(RP)perovskites(RPPs)with decent stability have captured the imagination of the photovoltaic research community and bring hope for boosting the development of perovskite solar cell(PSC)***,two-dimensional(2D)or quasi-2D RP PSCs are encountered with some challenges of the large exciton binding energy,blocked charge transport and poor film quality,which restrict their photovoltaic ***,these issues can be readily resolved by rationally designing spacer cations of *** review mainly focuses on how to design the molecular structures of organic spacers and aims to endow RPPs with outstanding photovoltaic *** firstly elucidated the important roles of organic spacers in impacting crystallization kinetics,charge transporting ability and stability of *** we brought three aspects to attention for designing organic ***,we presented the specific molecular structure design strategies for organic spacers of RPPs aiming to improve photovoltaic performance of RP *** proposed strategies in this review will provide new avenues to develop novel organic spacers for RPPs and advance the development of RPP photovoltaic technology for future applications.

关键词： Ruddlesden-Popper perovskites Low-dimensional perovskite solar cells Organic spacers Molecular structure Design strategies

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Recent progress on photoactive nonprecious transition-metal complexes

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science China Chemistry 2025年第1期 46-95页

作者： Zhong-Liang Gong Hong-Jie Zhang Yan Cheng Jianxun Liu Yuhan Ai Yaqin Li Zhihui Feng Qiong Zhang Shaolong Gong Yong Chen Chang-Jiang Yao Yuan-Yuan Zhu Liang-Jin Xu Yu-Wu Zhong CAS Key Laboratory of Photochemistry Institute of Chemistry Chinese Academy of Sciences State Key Laboratory of Structural Cemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences School of Chemistry and Chemical engineering Anhui Key Laboratory of Advanced Catalytic Materials and Reaction EngineeringHefei University of Technology State Key Laboratory of Explosion science and Safety Protection School of Mechatronical Engineering Beijing Institute of Technology College of Chemistry and Molecular sciences Hubei Key Lab on Organic and Polymeric Optoelectronic Materials Wuhan University School of Chemistry and Chemical engineering Anhui University Key Laboratory of Photochemical Conversion and Optoelectronic materials & CAS-HKU Joint Laboratory on New materials Technical Institute of Physics and Chemistry Chinese Academy of Sciences

Photoactive complexes of nonprecious transition metals, mainly including those in the first-row and partially the second-row of the Periodic table of elements, have received increasing attention in view of their low cost and long-term sustainability. They are recognized as promising alternatives to noble transition metal complex congeners that have been extensively studied in optoelectronic devices, artificial photosynthesis, photocatalysis, biodiagnostics, and therapeutics, etc. This review is devoted to a comprehensive summary on the classical and recent advances on photoactive nonprecious transition metal complexes, including photoactive Zr, V, Cr, Mo, and W complexes, Mn complexes and hybrids, Fe, Co, Ni, and Cu complexes, and Zn and Cd complexes and hybrids. A particular focus is given on the molecular design, modulation of photophysical and photochemical properties, and applications of the representative and lately-developed nonprecious metal complexes. In addition, a perspective on the future development in this field is provided at the end of this review.

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“One stone, two birds”: Salt template enabling porosity engineering and single metal atom coordinating toward high-performance zinc-ion capacitors

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Journal of Energy Chemistry 2025年第1期 637-645页

作者： Chunliu Zhu Huanyu Liang Ping Li Chenglong Qiu Jingyi Wu Jingwei Chen Weiqian Tian Yue Zhu Zhi Li Huanlei Wang School of materials science and engineering Ocean University of China department of Chemical and materials engineering University of Alberta

Zinc-ion hybrid capacitors （ZIHCs） have received increasing attention as energy storage devices owing to their low cost,high safety,and environmental ***,their progress has been hampered by low energy and power density,as well as unsatisfactory long-cycle stability,mainly due to the lack of suitable electrode *** this context,we have developed manganese single atoms implanted in nitrogen-doped porous carbon nanosheets （MnSAs/NCNs） using a metal salt template method as cathodes for *** metal salt serves a dual purpose in the synthesis process:It facilitates the uniform dispersion of Mn atoms within the carbon matrix and acts as an activating agent to create the porous *** applied in ZIHCs,the MnSAs/NCNs electrode demonstrates exceptional performance,including a high capacity of 203 m Ah g-1,an energy density of 138 Wh kg-1at 68 W kg-1,and excellent cycle stability with 91%retention over 10,000 *** calculations indicate that the introduced Mn atoms modulate the local charge distribution of carbon materials,thereby improving the electrochemical *** work demonstrates the significant potential of carbon materials with metal atoms in zinc-ion hybrid capacitors,not only in enhancing electrochemical performance but also in providing new insights and methods for developing high-performance energy storage devices.

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In situ construction of Cu(Ⅰ)-Cu(Ⅱ) pairs for efficient electrocatalytic nitrate reduction reaction to ammonia

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Journal of Energy Chemistry 2025年第1期 106-113页

作者： Muyun Zheng Yuchi Wan Leping Yang Shen Ao Wangyang Fu Zhengjun Zhang Zheng-Hong Huang Tao Ling Feiyu Kang Ruitao Lv State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Institute of New Energy materials and engineering School of Materials Science and Engineering Fuzhou University Key Laboratory of Advanced materials (MOE) School of Materials Science and Engineering Tsinghua University Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education Tianjin Key Laboratory of Composite and Functional Materials School of Materials Science and Engineering Tianjin University

Electrocatalytic nitrate reduction reaction （NO3-RR） to ammonia under ambient conditions is expected to be a green process for ammonia synthesis and alleviate water pollution *** report a CuO nanoparticles incorporated on nitrogen-doped porous carbon （CuO@NC） catalyst for *** of Cu（Ⅱ） is reduced to Cu（Ⅰ） during the NO3-RR process to construct Cu（Ⅰ）-Cu（Ⅱ） pairs,confirmed by in situ X-ray photoelectron spectroscopy （XPS） and Raman *** functional theory （DFT） calculations indicated that the formation of Cu（Ⅰ） could provide a reaction path with smaller energy barrier for NO3-RR,while Cu（Ⅱ） effectively suppressed the competition of hydrogen evolution reaction （HER）.As a result,CuO@NC catalyst achieved a Faradaic efficiency of 84.2% at -0.49 V versus reversible hydrogen electrode （RHE）,and a NH3yield rate of 17.2 mg *** -0.79 V ***,higher than the HaberBosch process (<3.4 g h-1g-1cat.).This work may open a new avenue for effective NO3-RR by modulating oxidation states.

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Recent Advances in Fibrous materials for Hydroelectricity Generation

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Nano-Micro Letters 2025年第2期17卷 109-133页

作者： Can Ge Duo Xu Xiao Feng Xing Yang Zheheng Song Yuhang Song Jingyu Chen Yingcun Liu Chong Gao Yong Du Zhe Sun Weilin Xu Jian Fang College of Textile and Clothing engineering Soochow UniversitySuzhou 215123People’s Republic of China National engineering Laboratory for Modern Silk Soochow UniversitySuzhou 215123People’s Republic of China State Key Laboratory of New Textile materials and Advanced Processing Technologies Wuhan Textile UniversityWuhan 430200People’s Republic of China Institute of Functional Nano&Soft materials(FUNSOM) Soochow UniversitySuzhou 215123People’s Republic of China department of Electrical and Computer engineering University of MassachusettsAmherstMA 01003USA department of materials Imperial College LondonSouth Kensington CampusLondon SW72AZUK College of Textile science and engineering Zhejiang Sci-Tech UniversityHangzhou 310018People’s Republic of China School of materials science and engineering Shanghai Institute of Technology100 Haiquan RoadShanghai 201418People’s Republic of China

Depleting fossil energy sources and conventional polluting power generation pose a threat to sustainable *** generation from ubiquitous and spontaneous phase transitions between liquid and gaseous water has been considered a promising strategy for mitigating the energy *** materials with unique flexibility,processability,multifunctionality,and practicability have been widely applied for fibrous materials-based hydroelectricity generation(FHG).In this review,the power generation mechanisms,design principles,and electricity enhancement factors of FHG are first ***,the fabrication strategies and characteristics of varied constructions including 1D fiber,1D yarn,2D fabric,2D membrane,3D fibrous framework,and 3D fibrous gel are ***,the advanced functions of FHG during water harvesting,proton dissociation,ion separation,and charge accumulation processes are analyzed in ***,the potential applications including power supply,energy storage,electrical sensor,and information expression are also ***,some existing challenges are considered and prospects for future development are sincerely proposed.

关键词： Hydroelectricity Fibrous material Streaming potential Ion diffusion

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Mechanism of influence of chloride ions on electrogenerative leaching of sulfide minerals

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Journal of Central South University of Technology 2006年第4期13卷 379-382页

作者：王少芬方正 depart ment of Chemistry and Environmental engineering Changsha University of Science and Technology School of Chemistry and Chemical engineering Central South University

A dual cell system was used to study the influence of chloride ions on the electrogenerative leaching of sulfide minerals. The results show that the influences of chloride ions on a series of electrogenerative leaching system are similar, and chlorine ion is involved in the electrogenerative leaching process of sulfide minerals directly. The output power increases with the increase of Cl^- concentration. The influence on the electrogenerative leaching rate decreases when the Cl^- concentration reaches a certain value. The mechanisms of anodic reaction are deduced based on the reasonable hypothesis, and kinetic equations with respect to chlorine ions for each sulfide mineral are obtained. The kinetic equations show that when concentration of Cl^- is relatively low, the electrogenerative leaching rates are predicted to have 2/5,3/7,1/3 and 1/3 order dependence on Cl^- concentration for chalcopyrite concentrate,nickel concentrate, sphalerite and galena. As concentration of Cl^- increases, the correlative dependence of electrogenerative leaching rate on concentration of Cl^- becomes weak.

关键词： chloride ion electrogenerative leaching mechanism sulfide minerals

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Preparation of Modified Composite Nanofiltration Membrane Synergistically Using Carboxylic Multi-walled Carbon Nanotube and β-cyclodextrin

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Journal of Wuhan University of Technology(materials science) 2025年第1期 232-239页

作者：刘鹏 MAO Junpeng FANG Yanfeng YU Yunwu CHEN Changxiu TANG Ning WAN Ye GU Yaxin LIU Yunxue WANG Lihua School of materials science and engineering Shenyang Jianzhu University

A new modified blend ultrafiltration （UF） membrane with good hydrophilicity,high porosity and excellent anti-fouling performance was developed by using carboxylic multi-walled carbon nanotube （CMWCNT） as casting solution ***,a composite nanofiltration （NF） membrane with large water flux and good retention rate was fabricated by using the PVDF/CMWCNT blend UF membrane as the substrate,and polyvinyl alcohol （PVA）,β-cyclodextrin （β-CD） and polyethylenimine （PEI） as the coating *** results show that with the appropriate addition of CMWCNT in the casting solution,the surface roughness,porosity and recovery rate of the PVDF/CMWCNT blend UF membrane is obviously *** water flux of blend UF membrane is significantly improved when the CMWCNT content increases from 0 wt% to 0.2 wt%.The water flux of blend UF membrane with 0.2 wt% CMWCNT is 162.7 L/（m2·h）,which is 44.3% higher than that of the pure PVDF *** β-CD content is 0.8 wt%,the retention rate of Congo red by PVDF/CMWCNT/β-CD composite NF membrane reaches 98.7%,which is 28.3% higher than that of single PVA/PEI modified *** research will provide a new idea and simple method for developing novel high-performance composite NF membranes.

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通过低浓度混合有机二硒化物和有机二碲化物有序串联促进安时级高能量密度锂硫电池中的硫氧化还原动力学（英文）

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science China materials 2025年第1期 207-216页

作者：周江奇舒程勇张千玉唐伟吴宇平 School of Chemical engineering and Technology Xi'an Jiaotong University School of Chemical engineering Kunming University of Science and Technology College of materials science and engineering Sichuan University School of Energy and Environment Southeast University

均相氧化还原介质可以有效缓解多硫化锂在锂硫电池中的穿梭效应和缓慢的氧化还原动力学,但由于多硫化锂的多步转化需要串联催化的多功能活性位点,因此无法实现多硫化物锂的完美性能.基于氧化还原共介导原理,本文提出了一种混合有机二硒...

均相氧化还原介质可以有效缓解多硫化锂在锂硫电池中的穿梭效应和缓慢的氧化还原动力学,但由于多硫化锂的多步转化需要串联催化的多功能活性位点,因此无法实现多硫化物锂的完美性能.基于氧化还原共介导原理,本文提出了一种混合有机二硒化物和有机二碲化物（混合-Se/Te）的促进剂,以诱导串联催化并提升多硫化锂的有效电化学转化.具体而言,二苯二硒化物促进了多硫化锂与硫之间的固-液和液-液转化,而二苯二碲化物则改善了硫化锂沉积的固-液转化.因此,即使在6.5 mg cm-2的高硫负载和5.88μL mg-1的低电解液/硫比下,10 mM的低浓度混合-Se/Te促进剂也提供了6.6 mAh cm-2的高放电容量和在0.5 C下4.1 mAh cm-2的良好倍率性能.此外,组装的1.5 Ah级锂硫软包电池在0.05 C时提供了332 Wh kg-1的能量密度和良好的循环稳定性.我们的研究展示了利用分离活性位点推动连续硫转化反应的适用性，并预计将激发针对能量相关氧还原反应的动力学促进剂的深度分子设计.

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Electrocatalytic nitrite reduction to ammonia on isolated bismuth alloyed ruthenium

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Journal of Energy Chemistry 2025年第1期 369-376页

作者： Shiyao Shang Fuzhou Wang Zeyi Sun Chaofan Qiang Ke Chu School of materials science and engineering Lanzhou Jiaotong University

Electrochemical reduction of NO2-to NH3（NO2-RR） is recognized as an appealing approach for achieving renewable NH3synthesis and waste ***,we report isolated Bi alloyed Ru （Bi1Ru） as an efficient NO2-RR *** calculations and in situ electrochemical measurements reveal the creation of Bi1-Ru dual sites which can remarkably promote NO2-activation and suppress proton adsorption,while accelerating the NO2-RR protonation energetics to render a high NO2--to-NH3conversion ***,Bi1Ru assembled in a flow cell delivers an NH3yield rate of 1901.4μmol h-1cm-2and an NH3-Faradaic efficiency of 94.3%at an industrial-level current density of 324.3 mA *** study offers new perspectives for designing and constructing p-block single-atom alloys as robust and high-current-density NO2-RR catalysts toward the ammonia electrosynthesis.

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Integration of Electrical Properties and Polarization Loss Modulation on Atomic Fe–N‑RGO for Boosting Electromagnetic Wave Absorption

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Nano-Micro Letters 2025年第2期17卷 517-532页

作者： Kaili Zhang Yuefeng Yan Zhen Wang Guansheng Ma Dechang Jia Xiaoxiao Huang Yu Zhou State Key Laboratory of Precision Welding&Joining of materials and Structures Harbin Institute of TechnologyHarbin 150001People’s Republic of China School of materials science and engineering Harbin Institute of TechnologyHarbin 150001People’s Republic of China MIIT Key Laboratory of Advanced Structural‑Functional Integration materials&Green Manufacturing Technology Harbin Institute of TechnologyHarbin 150001People’s Republic of China

Developing effective strategies to regulate graphene’s conduction loss and polarization has become a key to expanding its application in the electromagnetic wave absorption(EMWA)*** on the unique energy band structure of graphene,regulating its bandgap and electrical properties by introducing heteroatoms is considered a feasible ***,metal-nitrogen doping reduced graphene oxide(M–N-RGO)was prepared by embedding a series of single metal atoms M–N_(4) sites(M=Mn,Fe,Co,Ni,Cu,Zn,Nb,Cd,and Sn)in RGO using an N-coordination atom-assisted *** composites had adjustable conductivity and polarization to optimize dielectric loss and impedance matching for efficient EMWA *** results showed that the minimum reflection loss(RL_(min))of Fe–N-RGO reaches−74.05 dB(2.0 mm)and the maximum effective absorption bandwidth(EAB_(max))is 7.05 GHz(1.89 mm)even with a low filler loading of only 1 wt%.Combined with X-ray absorption spectra(XAFS),atomic force microscopy,and density functional theory calculation analysis,the Fe–N_(4) can be used as the polarization center to increase dipole polarization,interface polarization and defect-induced polarization due to d-p orbital hybridization and structural ***,electron migration within the Fe further leads to conduction loss,thereby synergistically promoting energy *** study demonstrates the effectiveness of metal-nitrogen doping in regulating the graphene′s dielectric properties,which provides an important basis for further investigation of the loss mechanism.

关键词： Electromagnetic wave absorption Fe-N-RGO Dipole polarization Conduction loss Impedance matching

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