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Design strategies for rechargeable aqueous metal-ion batteries

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Science China Chemistry 2024年第1期67卷 165-190页

作者： Yang Li Xin Zhao Yifu Gao Yichen Ding Zhichun Si Liubing Dong Dong Zhou feiyu kang Tsinghua Shenzhen International Graduate School Tsinghua UniversityShenzhen 518055China College of Chemistry and Materials Science Jinan UniversityGuangzhou 511443China

Rechargeable aqueous metal-ion batteries(AMBs)have attracted extensive scientific and commercial interest due to their potential for cost-effective,highly safe,and scalable stationary energy storage.However,their limited output voltage,inadequate energy density,and poor reversibility of ambiguous electrode reactions in aqueous electrolytes strongly limit their practical viability.This review aims to elucidate the challenges of existing AMBs from the material design to whole device applications.We summarize the emerging electrochemistry,fundamental properties,and key issues in interfacial behaviors of various classes of prevailing AMBs,including aqueous alkali metal-ion batteries and multivalent-ion batteries,and present an appraisal of recent advances for addressing the performance deficiency.Specifically,the progress of zinc-ion batteries is highlighted to provide a ubiquitous guideline for their commercialization in the grid-scale energy storage.Finally,we figure out the dominating general challenges for achieving high-performance AMBs,laying out a perspective for future breakthroughs.

关键词： aqueous metal-ion batteries aqueous alkali metal-ion batteries zinc-ion batteries interfacial behavior stationary energy storage

Roadmap for rechargeable batteries:present and beyond

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Science China Chemistry 2024年第1期67卷 13-42页

作者： Sen Xin Xu Zhang Lin Wang Haijun Yu Xin Chang Yu-Ming Zhao Qinghai Meng Pan Xu Chen-Zi Zhao Jiahang Chen Huichao Lu Xirui Kong Jiulin Wang Kai Chen Gang Huang Xinbo Zhang Yu Su Yao Xiao Shu-Lei Chou Shilin Zhang Zaiping Guo Aobing Du Guanglei Cui Gaojing Yang Qing Zhao Liubing Dong Dong Zhou feiyu kang Hu Hong Chunyi Zhi Zhizhang Yuan Xianfeng Li Yifei Mo Yizhou Zhu Dongfang Yu Xincheng Lei Jianxiong Zhao Jiayi Wang Dong Su Yu-Guo Guo Qiang Zhang Jun Chen Li-Jun Wan CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Sciences(BNLMS)Institute of ChemistryChinese Academy of Sciences(CAS)Beijing 100190China University of Chinese Academy of Sciences.Beijing 100049 China Institute of Advanced Battery Materials and Devices Faculty of Materials and ManufacturingBeijing University of TechnologyBeijing 100124China Key Laboratory of Advanced Functional Materials Ministry of EducationBeijing University of TechnologyBeijing 100124China Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology Department of Chemical EngineeringTsinghua UniversityBeijing 100084China State Key Laboratory of Chemistry and Utilization of Carbon-Based Energy Resources College of ChemistryXinjiang UniversityUrumqi 830046China Department of Chemical Engineering Shanghai Jiao Tong UniversityShanghai 200240China State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChangchun 130022China Institute for Carbon Neutralization College of Chemistry and Materials EngineeringWenzhou UniversityWenzhou 325035China School of Chemical Engineering and Advanced Materials The University of AdelaideAdelaide 5000Australia Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess TechnologyChinese Academy of SciencesQingdao 266101China Frontiers Science Center for New Organic Matter Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education)College of ChemistryNankai UniversityTianjin 300071China College of Chemistry and Materials Science Jinan UniversityGuangzhou 511443China Tsinghua Shenzhen International Graduate School Tsinghua UniversityShenzhen 518055China Department of Materials Science and Engineering City University of Hong KongHong Kong 999077China Division of Energy Storage Dalian National Laboratory for Clean Energy(DNL)Dalian Institute of Chem

Rechargeable batteries currently hold the largest share of the electrochemical energy storage market,and they play a major role in the sustainable energy transition and industrial decarbonization to respond to global climate change.Due to the increased popularity of consumer electronics and electric vehicles,lithium-ion batteries have quickly become the most successful rechargeable batteries in the past three decades,yet growing demands in diversified application scenarios call for new types of rechargeable batteries.Tremendous efforts are made to developing the next-generation post-Li-ion rechargeable batteries,which include,but are not limited to solid-state batteries,lithium–sulfur batteries,sodium-/potassium-ion batteries,organic batteries,magnesium-/zinc-ion batteries,aqueous batteries and flow batteries.Despite the great achievements,challenges persist in precise understandings about the electrochemical reaction and charge transfer process,and optimal design of key materials and interfaces in a battery.This roadmap tends to provide an overview about the current research progress,key challenges and future prospects of various types of rechargeable batteries.New computational methods for materials development,and characterization techniques will also be discussed as they play an important role in battery research.

关键词： energy storage rechargeable batteries battery materials electrochemistry

Progress on metal-support interactions in Pd-based catalysts for automobile emission control

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Journal of Environmental Sciences 2023年第3期125卷 401-426页

作者： Yidan Cao Rui Ran Xiaodong Wu Zhichun Si feiyu kang Duan Weng Institute of Materials Research Tsinghua Shenzhen International Graduate SchoolTsinghua UniversityShenzhen 518055China Tsinghua-Berkeley Shenzhen Institute Tsinghua UniversityShenzhen 518055China School of Materials Science and Engineering Tsinghua UniversityBeijing 100084China

The interactions between metals and oxide supports,so-called metal-support interactions(MSI),are of great importance in heterogeneous catalysis.Pd-based automotive exhaust control catalysts,especially Pd-based three-way catalysts (TWCs),have received considerable research attention owing to its prominent oxidation activity of HCs/CO,as well as excellent thermal stability.For Pd-based TWCs,the dispersion,chemical state and thermal stability of Pd species,which are crucial to the catalytic performance,are closely associated with interactions between metal nanoparticles and their supporting matrix.Progress on the research about MSI and utilization of MSI in advanced Pd-based three-way catalysts are reviewed here.Along with the development of advanced synthesis approaches and engine control technology,the study on MSI would play a notable role in further development of catalysts for automobile exhaust control.

关键词： Palladium Three-way catalysts(TWCs) Metal-support interaction Oxide supports

The dynamic surface evolution of halide perovskites induced by external energy stimulation

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National Science Review 2024年第4期11卷 185-194页

作者： feiyu Cheng Pengdong Wang Chenzhe Xu Qingliang Liao Suicai Zhang Haochun Sun Wenqiang Fan Guodong Liu Zhiyun Li Yaping Kong Li Wang Fangsen Li Zhuo kang Yue Zhang Academy for Advanced Interdisciplinary Science and Technology State Key Laboratory for Advanced Metals and Materials University of Science and Technology Beijing Beijing Key Laboratory for Advanced Energy Materials and Technologies Key Laboratory of Advanced Materials and Devices for Post-Moore ChipsMinistry of EducationBeijing Advanced Innovation Center for Materials Genome Engineering School of Materials Science and EngineeringUniversity of Science and Technology Beijing Vacuum Interconnected Nanotech Workstation(Nano-X) Suzhou Institute of Nano-Tech and Nano-BionicsChinese Academy of Sciences Beijing National Laboratory for Condensed Matter Physics Institute of Physics Chinese Academy of Sciences

Tracking the dynamic surface evolution of metal halide perovskite is crucial for understanding the corresponding fundamental principles of photoelectric properties and intrinsic instability. However, due to the volatility elements and soft lattice nature of perovskites, several important dynamic behaviors remain unclear. Here, an ultra-high vacuum（UHV） interconnection system integrated by surface-sensitive probing techniques has been developed to investigate the freshly cleaved surface of CH3NH3PbBr3in situ under given energy stimulation. On this basis, the detailed three-step chemical decomposition pathway of perovskites has been clarified. Meanwhile, the evolution of crystal structure from cubic phase to tetragonal phase on the perovskite surface has been revealed under energy stimulation. Accompanied by chemical composition and crystal structure evolution, electronic structure changes including energy level position,hole effective mass, and Rashba splitting have also been accurately determined. These findings provide a clear perspective on the physical origin of optoelectronic properties and the decomposition mechanism of perovskites.

关键词： metal halide perovskite external energy stimulation surface dynamic evolution surface electronic structure ultra-high vacuum interconnection system

ZnS-assisted evolution of N,S-doped hierarchical porous carbon nanofiber membrane with highly exposed Fe-N_(4)/C_(x) sites for rechargeable Zn-air battery

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Journal of Energy Chemistry 2022年第12期75卷 430-440,I0011页

作者： Leping Yang Lingxiao Yu Zheng-Hong Huang feiyu kang Ruitao Lv State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China Key Laboratory of Advanced Materials(MOE) School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China Institute of Materials Research Tsinghua Shenzhen International Graduate SchoolTsinghua UniversityShenzhen 518055GuangdongChina

Binder-free bifunctional electrocatalysts are attractive for rechargeable Zn-air batteries(ZABs)in gridscale energy storage and flexible electronics,but suffering from the sluggish mass transport and inadequate catalytic capability.Herein,we propose a scalable approach of in-situ engineering highly exposed Fe-N_(4)/Cxsites on the N,S-doped porous carbon nanofiber membrane as a binder-free air electrode catalyst for ZABs.ZnS nanospheres are firstly used as integrated structure-directing agents to facilitate the electronic modulation of Fe-N_(4)/Cxsites by S doping and construct the hierarchical macro/meso/micropores at high temperature.Neither additional step for removal of ZnS nanospheres nor doping process is required,significantly simplifying the pore formation process and improving the S doping efficiency.Benefiting from the enhanced intrinsic activity of high-density Fe-N_(4)/Cxsites(23.53μmol g^(-1))and the optimized mass transport of carbon nanofibers,as-synthesized electrocatalyst shows a positive half-wave potential of 0.89 V for oxygen reduction reaction and a small overpotential of 0.47 V at 10 m A cm^(-2)for oxygen evolution reaction.When used as the air cathode catalyst for ZABs,it delivers a high specific capacity of 699 m Ah g^(-1)at 5 m A cm^(-2),a large peak power density of 228 m W cm^(-2)and a prolonged cycling over 1000 h.At 10 m A cm^(-2),a robust structure with atomically dispersed Fe is also remained after cycling for 420 h.Due to the flexible properties of the electrocatalyst,as-assembled quasi-solid-state ZAB shows stable cycling over 90 h at alternately flat/bent states,demonstrating great prospects in flexible electronic device applications.

关键词： Electrospinning Single-atom catalysts Fe-N_(4)/C_(x) Oxygen electrocatalysis Zn-air batteries

Optimize two-phase distribution of lithium-rich materials to stabilize structure and suppress voltage attenuation

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International Journal of Minerals,Metallurgy and Materials 2022年第12期29卷 2201-2211页

作者： Yang Yu Jianling Li Guimei Han Zhe Yang Jianjian Zhong feiyu kang State Key Laboratory of Advanced Metallurgy School of Metallurgical and Ecological EngineeringUniversity of Science and Technology BeijingBeijing 100083China Chinese Research Academy of Environmental Sciences Beijing 100012China School of Materials Science and Engineering Tsinghua UniversityBeijing 100084China

Lithium-rich materials possess the ultra-high specific capacity,but the redox of oxygen is not completely reversible,resulting in voltage attenuation and structural instability.A stepwise co-precipitation method is used for the first time in this paper to achieve the control of the two-phase distribution through controlling the distribution of transition metal elements and realize the modification of particle surface structure without the aid of heterologous ions.The results of characterization tests show that the content of LiMO_(2) phase inside the particles and the content of Li_(2)MnO_(3) phase on the surface of the particles are successfully increased,and the surface induced formation of Li_(4)Mn_(5)O_(12) spinel phase or some disorderly ternary.The electrochemical performance of the modified sample is as follows:LR(pristine)shows specific discharge capacity of 72.7 mA·h·g^(−1)after 500 cycles at 1 C,while GR(modified sample)shows specific discharge capacity of 137.5 mA·h·g^(−1) at 1 C,and the discharge mid-voltage of GR still remains above 3 V when cycling to 220 cycles at 1 C(mid-voltage of LR remains above 3 V when cycling to 160 cycles at 1 C).Therefore,deliberately regulating the local state of the two phases is a successful way to reinforced the material structure and inhibition the voltage attenuation.

关键词： lithium-rich phase tuning engineering stepwise co-precipitation voltage attenuation 1.Introduction

Electrostatic Interaction Tailored Anion-Rich Solvation Sheath Stabilizing High-Voltage Lithium Metal Batteries

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Nano-Micro Letters 2022年第9期14卷 147-159页

作者： Junru Wu Ziyao Gao Yao Wang Xu Yang Qi Liu Dong Zhou Xianshu Wang feiyu kang Baohua Li Tsinghua Shenzhen International Graduate School Tsinghua UniversityShenzhen 518055People’s Republic of China School of Materials Science and Engineering Tsinghua UniversityBeijing 100084People’s Republic of China College of Materials Science and Engineering Hunan UniversityChangsha 410082People’s Republic of China

Through tailoring interfacial chemistry,electrolyte engineering is a facile yet effective strategy for highperformance lithium(Li)metal batteries,where the solvation structure is critical for interfacial chemistry.Herein,the effect of electrostatic interaction on regulating an anion-rich solvation is firstly proposed.The moderate electrostatic interaction between anion and solvent promotes anion to enter the solvation sheath,inducing stable solid electrolyte interphase with fast Li+transport kinetics on the anode.This asdesigned electrolyte exhibits excellent compatibility with Li metal anode(a Li deposition/stripping Coulombic efficiency of 99.3%)and high-voltage LiCoO_(2) cathode.Consequently,the 50μm-thin Li||high-loading LiCoO_(2) cells achieve significantly improved cycling performance under stringent conditions of high voltage over 4.5 V,lean electrolyte,and wide temperature range(-20 to 60℃).This work inspires a groundbreaking strategy to manipulate the solvation structure through regulating the interactions of solvent and anion for highperformance Li metal batteries.

关键词： Electrostatic interaction Anion-rich solvation sheath High voltage Lithium metal batteries Wide temperature range

Photoluminescence manipulation in two-dimensional transition metal dichalcogenides

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Journal of Materiomics 2023年第4期9卷 768-786页

作者： Minglang Gao Lingxiao Yu Qian Lv feiyu kang Zheng-Hong Huang Ruitao Lv State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijing100084China Key Laboratory of Advanced Materials(MOE) School of Materials Science and EngineeringTsinghua UniversityBeijing100084China Institute of Materials Research Shenzhen International Graduate SchoolTsinghua UniversityShenzhen518055China

Two-dimensional transition metal dichalcogenides(TMDCs)have been regarded as an intriguing platform for exploring novel physical phenomena and optoelectronic devices due to their excitonic emission characteristics derived from the atomic thin thickness and reduced dielectric screening effect.Notably,monolayer TMDCs with a direct bandgap exhibiting strong photoluminescence(PL)are promising candidates for the light-emitting devices,while the interlayer excitons in heterostructures hold great potential for the photonic chips and optical communication applications.However,the non-ideal photoluminescent intensity and quality due to the ultrathin thickness and high defect density of experimentally obtained monolayer TMDCs limit the further development for the light-emission applications.Here,we summarize the research progress on the PL manipulation of the excitonic emission in TMDCs,where the PL intensity enhancement and emission wavelength regulation are included.The concept and characteristics of excitons are overviewed firstly,followed by the discussion on the evaluation and characterization of excitonic emission.The state-of-the-art progress on the manipulation of the neutral excitons and interlayer excitons PL are then summarized.Finally,the challenges and prospects are proposed.

关键词： 2D materials TMDCs Neutral exciton Interlayer exciton Photoluminescence enhancement

An isolation strategy to anchor atomic Ni or Co cocatalysts on TiO_(2)(A)for photocatalytic hydrogen production

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Nano Research 2022年第7期15卷 5848-5856页

作者： Shangchun Lv Mengxi Pei Yuxiang Liu Zhichun Si Xiaodong Wu Rui Ran Duan Weng feiyu kang International Graduate School at Shenzhen Tsinghua UniversityShenzhen 518055China The Key Laboratory of Advanced Materials of Ministry of Education School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China

TiO_(2) has been considered as an ideal photocatalyst for water splitting.However,narrow light absorbance,low charge separation efficiency,and rare surface active sites lead to the low photocatalytic efficiency of TiO_(2).Although extensive research attempted to improve the situation,there is still lack of method for constructing high active and noble-metal-free TiO_(2) photocatalyst for H_(2) evolution reactions(HER).In this work,we loaded single atomic(SA)Ni(or Co)on the surface of anatase TiO_(2)(TiO_(2)(A))nanosheets by an isolation strategy.Ethylene diamine tetraacetic acid and ethylene glycol(EDTA-EG)compounds were used to chelate metal ions in solution and form carbon quantum dots in the following thermal treatment to isolate the metal ions on surface of TiO_(2)(A).The prepared Ni SA/TiO_(2)(A)catalyst owned a“skin wrapped body”structure with in-situ formed twodimensional(2D)heterojunction facilitating the fast electron transfer.As a result,the Ni SA/TiO_(2)(A)catalyst showed a high H_(2) evolution rate of 2,900μmol·g−1·h−1.This work provides an isolation strategy for constructing promising single-atom metal catalyst for photocatalysis and beyond.

关键词： Ni or Co single atoms cocatalyst anatase TiO_(2)(TiO_(2)(A)) photocatalytic H_(2)evolution