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High performance and stable pure-blue quasi-2D perovskite light-emitting diodes by multifunctional zwitterionic passivation engineering

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Advanced Photonics 2024年第2期6卷 32-40页

作者： Chao Shen Shuyan Fang Jibin Zhang Xiangfei Liang Chenhui Su Jian Qing Wanzhu Cai Yunhan Luo Renqiang Yang Lintao Hou Jinan University College of Physics and Optical EngineeringGuangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy MaterialsGuangzhou Key Laboratory of Vacuum Coating Technologies and New Energy MaterialsGuangzhouChina Jinan University College of Physics and Optical EngineeringGuangdong Provincial Key Laboratory of Optical Fiber Sensing and CommunicationsGuangzhouChina Zhengzhou University School of Physics and MicroelectronicsKey Laboratory of Materials Physics of Ministry of EducationZhengzhouChina Jinan University Key Laboratory of Optoelectronic Information and Sensing Technologies of Guangdong Higher Education InstitutesGuangzhouChina Jianghan University School of Optoelectronic Materials and TechnologyKey Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of EducationWuhanChina

Despite the rapid advances of red and green perovskite light-emitting diodes(Pe LEDs),achieving high brightness with high external quantum efficiency(EQE)remains a challenge for the pure-blue Pe LEDs,which greatly hinders their practical applications,such as white-light illumination and in optical communication as a high-speed and low-loss light source.Herein,we report a high-performance pure-blue Pe LED based on mixed-halide quasi-2D perovskites incorporated with a zwitterionic molecule of 3-(benzyldimethylammonio)propanesulfonate(3-BAS).Experimental and density functional theory analysis reveals that 3-BAS can simultaneously eliminate non-radiative recombination loss,suppress halide migration,and regulate phase distribution for smoothing energy transfer in the mixed-halide quasi-2D perovskites,leading to the final perovskites with high photoluminescence quantum yield and robust spectrum stability.Thus,the highperformance pure-blue Pe LED with a recorded brightness with 1806 cd m-2and a relative higher EQE of 9.25%is achieved,which is successfully demonstrated in a visible light communication system for voice signal transmission.We pave the way for achieving highly efficient pure-blue Pe LEDs with great application potential in future optical communication networks.

关键词： pure-blue PeLEDs quasi-2D perovskite zwitterionic additive visible light communication

Dimethylamine oxalate manipulating CsPbI_(3) perovskite film crystallization process for high efficiency carbon electrode based perovskite solar cells

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Journal of energy Chemistry 2024年第6期93卷 221-228,I0006页

作者： Wenran Wang Xin Peng Jianxin Zhang Jiage Lin Rong Huang Guizhi Zhang Huishi Guo Zhenxiao Pan Xinhua Zhong Huashang Rao key laboratory for Biobased Materials and energy of Ministry of Education College of Materials and EnergySouth China Agricultural UniversityGuangzhou 510642GuangdongChina College of Chemistry and Civil Engineering Shaoguan UniversityShaoguan 512005GuangdongChina guangdong provincial key laboratory of Utilization and Conservation of Food and Medicinal Resources in Northern Region Shaoguan UniversityShaoguan 512005GuangdongChina

Crystallization process determines the quality of perovskite films and the performances of resultant perovskite solar cells(PSCs).Dimethylamine oxalate has been proven as a multifunctional modulator,and is explored as an efficient additive in manipulating the crystallization process of CsPbI_(3) perovskite films.On one hand,oxalate serves as the precipitator that facilitates the nucleation process of intermediate.The larger size of intermediate is conductive to the larger size and smaller grain boundaries of resultant perovskite.On the other hand,in subsequent annealing process,the phase conversion and growth process of transient perovskite can be decelerated due to the strong interactions of oxalate with both dimethylamine cation(DMA^(+))and Pb^(2+).Due to the optimized crystallization kinetics,the morphology and quality of CsPbI_(3) perovskite films are comprehensively improved with lower defect concentrations,and charge recombination loss is effectively suppressed.Benefiting from the optimized crystal quality of perovskite films,the carbon electrode-based CsPbI_(3) PSCs exhibit a champion efficiency of 18.48%.This represents one of the highest levels among all hole transport layer-free inorganic perovskite solar cells.

关键词： Solar cells Perovskite CsPbI_(3) Carbon electrodes Oxalate

Regulating^(*)COOH intermediate via amino alkylation engineering for exceptionally effective photocatalytic CO_(2) reduction

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Journal of energy Chemistry 2024年第5期92卷 282-291页

作者： Chengcheng Chen Qiaoyu Zhang Fangting Liu Zhengguo Zhang Qiong Liu Xiaoming Fang key laboratory of Enhanced Heat Transfer and energy Conservation The Ministry of EducationSchool of Chemistry and Chemical EngineeringSouth China University of TechnologyGuangzhou 510640GuangdongChina guangdong provincial key laboratory of Chemical Measurement and Emergency Test Technology(China) Institute of AnalysisGuangdong Academy of Sciences(China National Analytical CenterGuangzhou)Guangzhou 510070GuangdongChina guangdong Engineering Technology Research Center of Efficient Heat Storage and application South China University of TechnologyGuangzhou 510640GuangdongChina guangdong provincial key laboratory of Fuel Cell Technology South China University of TechnologyGuangzhou 510640GuangdongChina

Photocatalytic reduction of CO_(2) into fuel represents a promising approach for achieving carbon neutrality,while realizing high selectivity in this process is challenging due to uncontrollable reaction intermediate and retarded desorption of target products.Engineering the interface microenvironment of catalysts has been proposed as a strategy to exert a significant influence on reaction outcomes,yet it remains a significant challenge.In this study,amino alkylation was successfully integrated into the melem unit of polymeric carbon nitrides(PCN),which could efficiently drive the photocatalytic CO_(2) reduction.Experimental characterization and theoretical calculations revealed that the introduction of amino alkylation lowers the energy barrier for CO_(2) reduction into^(*)COOH intermediate,transforming the adsorption of^(*)COOH intermediate from the endothermic to an exothermic process.Notably,the as-prepared materials demonstrated outstanding performance in photocatalytic CO_(2) reduction,yielding CO_(2)at a rate of 152.8μmol h^(-1) with a high selectivity of 95.4%and a quantum efficiency of 6.6%.

关键词： Polymeric carbonnitride Regulate intermediate Photocatalytic CO_(2)reduction Amino alkylation ^(*)COOH adsorption

Interfacial built-in electric field and crosslinking pathways enabling WS_(2)/Ti_(3)C_(2)T_(x) heterojunction with robust sodium storage at low temperature

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Journal of energy Chemistry 2024年第2期89卷 635-645,I0014页

作者： Jiabao Li Shaocong Tang Jingjing Hao Quan Yuan Tianyi Wang Likun Pan Jinliang Li Shenbo Yang Chengyin Wang College of Chemistry and Chemical Engineering Yangzhou UniversityYangzhou 225002JiangsuChina Shanghai key laboratory of Magnetic Resonance School of Physics and Electronic Science East China Normal UniversityShanghai 200241China Siyuan laboratory Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy MaterialsGuangdong Provincial Key Laboratory of Nanophotonic ManipulationDepartment of PhysicsJinan UniversityGuangzhou 510632GuangdongChina Hongzhiwei Technology(Shanghai)CO.LTD Shanghai 200241China

Developing efficient energy storage for sodium-ion batteries(SIBs)by creating high-performance heterojunctions and understanding their interfacial interaction at the atomic/molecular level holds promise but is also challenging.Besides,sluggish reaction kinetics at low temperatures restrict the operation of SIBs in cold climates.Herein,cross-linking nanoarchitectonics of WS_(2)/Ti_(3)C_(2)T_(x) heterojunction,featuring built-in electric field(BIEF),have been developed,employing as a model to reveal the positive effect of heterojunction design and BIEF for modifying the reaction kinetics and electrochemical activity.Particularly,the theoretical analysis manifests the discrepancy in work functions leads to the electronic flow from the electron-rich Ti_(3)C_(2)T_(x) to layered WS_(2),spontaneously forming the BIEF and“ion reservoir”at the heterogeneous interface.Besides,the generation of cross-linking pathways further promotes the transportation of electrons/ions,which guarantees rapid diffusion kinetics and excellent structure coupling.Consequently,superior sodium storage performance is obtained for the WS_(2)/Ti_(3)C_(2)T_(x) heterojunction,with only 0.2%decay per cycle at 5.0 A g^(-1)(25℃)up to 1000 cycles and a high capacity of 293.5 mA h g^(-1)(0.1A g^(-1)after 100 cycles)even at-20℃.Importantly,the spontaneously formed BIEF,accompanied by“ion reservoir”,in heterojunction provides deep understandings of the correlation between structure fabricated and performance obtained.

关键词： WS_(2)/Ti_(3)C_(2)T_(x)heterojunction Built-in electric field Ion reservoir Reaction kinetics Sodium storage performance at low temperature

Enhancing hydrogen evolution and oxidation kinetics through oxygen insertion into nickel lattice

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Journal of energy Chemistry 2024年第8期95卷 529-539页

作者： Wanli Liang Xiyu Gong Jinchang Xu Zixuan Dan Fanyan Xie Hulei Yu Hao-Fan Wang Yanshuo Jin Hongjuan Wang Yonghai Cao Hui Meng Hao Yu School of Chemistry and Chemical Engineering South China University of Technology Siyuan laboratory Guangzhou Key Laboratory of Vacuum Coating Technologies and New Energy Materials Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials Guangdong Provincial Key Laboratory of Optical Fiber Sensing and Communications Department of Physics Jinan University GBA Branch of Aerospace Information Research Institute Chinese Academy of Sciences Instrumental Analysis & Research Center Sun Yat-sen University School of Materials Science and Engineering South China University of Technology

Nickel-based materials,including metallic Ni and Ni oxide,have been widely studied in the exploration of non-precious-metal hydrogen electrocatalysts,but neither pure Ni nor NiO is ideal for the hydrogen evolution reaction（HER） and hydrogen oxidation reaction（HOR）.In this paper,an oxygen insertion strategy was applied on nickel to regulate its hydrogen electrocatalytic performance,and the oxygen-inserted nickel catalyst was successfully obtained with the assistance of tungsten dioxide support（denoted as O-Ni/WO2）.The partial insertion of oxygen in Ni maintains the face-centered cubic arrangement of Ni atoms,simultaneously expanding the lattice and increasing the lattice spacing.Consequently,the adsorption strength of*H and*OH on Ni is optimized,thus resulting in superior electrocatalytic performance of0-Ni/WO2in alkaline HER/HOR.The Tafel slope of O-Ni/WO2@NF for HER is 56 mV dec-1,and the kinetic current density of O-Ni/WO2for HOR reaches 4.85 mA cm-2,which is ahead of most currently reported catalysts.Our proposed strategy of inserting an appropriate amount of anions into the metal lattice could provide more possibilities for the design of high-performance catalysts.

关键词： Adsorption free energy Hydrogen evolution Hydrogen oxidation Nickel Oxygen insertion

Polar solvent induced in-situ self-assembly and oxygen vacancies on Bi_(2)MoO_(6)for enhanced photocatalytic degradation of tetracycline

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Nano Research 2024年第6期17卷 4951-4960页

作者： Fangyan Liu Dongyue Su Weizhen Liu Baiquan Liu Chuan Liu Hong Wang Mengye Wang State key laboratory of Optoelectronic Materials and technologies Guangdong Province Key Laboratory of Display Material and TechnologySchool of Electronics and Information TechnologySun Yat-Sen UniversityGuangzhou 510275China School of Materials Sun Yat-Sen UniversityShenzhen 518107China School of Environment and energy Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and RecyclingSouth China University of TechnologyGuangzhou 510006China

It has been proved to be an effective route to efficiently ameliorate photocatalytic performance of catalysts via designing three-dimensional(3D)hierarchical nanostructures and constructing oxygen vacancies(VOs).However,controlling the self-assembly of organization into 3D hierarchical nanostructures while introducing VOs in photocatalysts remains a challenge.Herein,we reported an ethylene glycol(EG)mediated approach to craft 3D hydrangea-structure Bi_(2)MoO_(6)with VOs for efficient photocatalytic degradation of tetracycline.Through manipulating the EG concentration during the fabrication process,the influence of EG concentration on the Bi_(2)MoO_(6)structure was systematically investigated.EG could promote the self-assembly of Bi_(2)MoO_(6)nanosheets to form a 3D hierarchical structure.Compared with 2D nanoplates,3D hierarchical architecture enhanced the surface area and the amount of active sites of Bi_(2)MoO_(6).In addition,the reduction effect of EG on metallic oxide enabled the generation of VOs in Bi_(2)MoO_(6).The VOs adjusted the electronic structure of Bi_(2)MoO_(6),which not only enhanced the light harvesting,but also facilitated the simultaneous utilization of photo-induced electrons and holes to form reactive oxygen species(·O2−and·OH)for the efficient tetracycline decomposition.3D Bi_(2)MoO_(6)hydrangea with VOs achieved a 79.4%removal efficiency of tetracycline after 75 min.This work provides a simple yet robust EG-mediated strategy,which not only promotes the self-assembly of nano-catalysts into 3D hierarchical architectures,but also crafts tunable VOs for highly efficient photocatalysis.

关键词： three-dimensional(3D)hierarchical nanostructures tunable oxygen vacancies ethylene glycol(EG)-mediated strategy bismuth molybdate photocatalytic degradation tetracycline

Nitrogen-doped titanium dioxide/schwertmannite nanocomposites as heterogeneous photo-Fenton catalysts with enhanced efficiency for the degradation of bisphenol A

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Journal of Environmental Sciences 2024年第9期143卷 1-11页

作者： Xing-Xing Qiao Yu-Hang Xu Xiang-Ji Liu Sai-Le Chen Zhou Zhong Ya-Feng Li Jian Lü Fujian provincial key laboratory of Soil Environmental Health and Regulation College of Resources and EnvironmentFujian Agriculture and Forestry UniversityFuzhou 350002China State key laboratory of Photocatalysis on energy and Environment Fuzhou UniversityFuzhou 350116China

Potential health risks related to environmental endocrine disruptors(EEDs)have aroused research hotspots at the forefront of water treatment technologies.Herein,nitrogen-doped titanium dioxide/schwertmannite nanocomposites(N-TiO_(2)/SCH)have been successfully developed as heterogeneous catalysts for the degradation of typical EEDs via photo-Fenton processes.Due to the sustainable Fe(Ⅲ)/Fe(Ⅱ)conversion induced by photoelectrons,as-prepared N-TiO_(2)/SCH nanocomposites exhibit much enhanced efficiency for the degradation of bisphenol A(BPA;ca.100% within 60 min under visible irradiation)in a wide pH range of 3.0-7.8,which is significantly higher than that of the pristine schwertmannite(ca.74.5%)or N-TiO_(2)(ca.10.8%).In this photo-Fenton system,the efficient degradation of BPA is mainly attributed to the oxidation by hydroxyl radical(·OH)and singlet oxygen(^(1)O_(2)).Moreover,the possible catalytic mechanisms and reaction pathway of BPA degradation are systematically investigated based on analytical and photoelectrochemical analyses.This work not only provides a feasible means for the development of novel heterogeneous photo-Fenton catalysts,but also lays a theoretical foundation for the potential application of mineral-based materials in wastewater treatment.

关键词： Titanium dioxide Schwertmannite Fenton reaction Environmental endocrine disruptors Photocatalysis

H-and J-aggregation of conjugated small molecules in organic solar cells

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Journal of energy Chemistry 2024年第6期93卷 174-192,I0005页

作者： Qiaoqiao Zhao Feng He State key laboratory of Biobased Material and Green Papermaking Qilu University of TechnologyShandong Academy of SciencesJinan 250353ShangdongChina Shenzhen Grubbs Institute and Department of Chemistry Southern University of Science and TechnologyShenzhen 518055GuangdongChina guangdong provincial key laboratory of Catalysis Southern University of Science and TechnologyShenzhen 518055GuangdongChina

As H-and J-aggregation receive more and more attention in the research of organic solar cells(OSCs),especially in small molecular systems,deep understanding of aggregation behavior is needed to guide the design of conjugated small molecular structure and the fabrication process of OSC device.For this end,this review is written.Here,the review firstly introduced the basic information about H-and J-aggregation of conjugated small molecules in OSCs.Then,the characteristics of H-and J-aggregation and the methods to identify them were summarized.Next,it reviewed the research progress of H-and J-aggregation of conjugated small molecules in OSCs,including the factors influencing H-and J-aggregation in thin film and the effects of H-and J-aggregation on OPV performance.

关键词： H-aggregation J-aggregation Organic solar cells Small molecules efficiency Stability

Optimization of the methane production in batch anaerobic digestion of maize straw by adjustment of total solid and substrate-to-inoculum ratio based on kinetics

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International Journal of Agricultural and Biological Engineering 2024年第1期17卷 225-231页

作者： Feng Zhen Tao Xing Lianhua Li Yongming Sun Hongqiong Zhang Guangzhou Institute of energy Conversion Chinese Academy of SciencesGuangzhou 510640China guangdong provincial key laboratory of New and Renewable energy Research and Development Guangzhou 510640China College of Engineering Northeast Agricultural UniversityHarbin 150030China

Anaerobic digestion(AD)operating under conditions of organic overload stress typically exacerbates the potential for process instability,thereby resulting in significant economic and ecological ramifications.In this investigation,an augmented substrate-to-inoculum ratio(S/I)along with varying total solid content(TS)levels was employed to replicate diverse organic loadings,utilizing maize straw and cattle manure.The findings reveal that a moderate augmentation in S/I and TS proves advantageous in augmenting methane yield,while an excessive substrate loading diminishes methane yield,hampers the kinetics of methane production,and even induces severe process instability.Kinetic study also displayed the variation of the model parameters for the first-order model,the modified Gompertze model,and the transfer function model.Both the modified Gompertze model and transfer function model exhibited the same environmental stress trend.Thus,both the increase in particulate content and the increase in S/I had a substantial effect on the substrate conversion rate to methane.Microbial analysis demonstrates the dominant influence of Firmicutes and Methanosarcina under different organic loading stresses.From both a kinetic and a microbiological point of view,this work provides novel insights into the fundamental processes that regulate anaerobic digestion(AD)under varying loading stress.Furthermore,it has significant implications for improving the operating efficiency of AD,which is a significant benefit.

关键词： maize straw dry anaerobic digestion methane production microbial characteristics kinetic model