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Catalyst–Support Interaction in Polyaniline‑Supported ni_(3)Fe Oxide to Boost Oxygen Evolution Activities for Rechargeable Zn‑Air Batteries

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nano-Micro Letters 2025年第1期17卷 176-190页

作者： Xiaohong Zou Qian Lu Mingcong Tang Jie Wu Kouer Zhang Wenzhi Li Yunxia Hu Xiaomin Xu Xiao Zhang Zongping Shao liang An Department of Mechanical Engineering The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment TechnologySchool of Environmental Science and TechnologyNanjing University of Information Science and TechnologyNanjing 210044People’s Republic of China Department of Chemistry The Chinese University of Hong KongMa Lin BuildingShatinHong Kong SAR 999077People’s Republic of China WA School of Mines:Minerals Energy and Chemical Engineering(WASM‑MECE)Curtin UniversityPerthWA 6102Australia Research Institute for Advanced Manufacturing The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China Research Institute for Smart Energy The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China

Catalyst–support interaction plays a crucial role in improving the catalytic activity of oxygen evolution reaction(OER).Here we modulate the catalyst–support interaction in polyaniline-supported ni_(3)Fe oxide(ni_(3)Fe oxide/PAnI)with a robust hetero-interface,which significantly improves oxygen evolution activities with an overpotential of 270 mV at 10 mA cm^(-2)and specific activity of 2.08 mA cm_(ECSA)^(-2)at overpotential of 300 mV,3.84-fold that of ni_(3)Fe *** is revealed that the catalyst–support interaction between ni_(3)Fe oxide and PAnI support enhances the ni–O covalency via the interfacial ni–n bond,thus promoting the charge and mass transfer on ni_(3)Fe *** the excellent activity and stability,rechargeable Zn-air batteries with optimum ni_(3)Fe oxide/PAnI are assembled,delivering a low charge voltage of 1.95 V to cycle for 400 h at 10 mA cm^(-2).The regulation of the effect of catalyst–support interaction on catalytic activity provides new possibilities for the future design of highly efficient OER catalysts.

关键词： Catalyst-support interaction Supported catalysts Heterointerface Oxygen evolution reaction Zn-air batteries

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Buried interface bridging for inverted cesium-formamidinium triiodide perovskite solar cells with long operational stability

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Science China Chemistry 2025年第1期68卷 163-173页

作者： Chenhui Zhang chunj.n liang Fulin Sun Ting Zhu Xinghai Huang Yuzhu Guo Xinyu Guo Kunyang Ge Dan Li Fangtian You Zhiqun He Key Laboratory of Luminescence and Optical Information Ministry of Education Institute of Optoelectronic TechnologyBeijing Jiaotong University Department of Physics School of Physical Science and Engineering Beijing Jiaotong University

In the field of perovskite solar cells(PSCs), the research on defects in the buried interface has been relatively limited due to its non-exposure; however, this interface significantly impacts the performance enhancement of inverted PSCs. This study employs phenylethylammonium chloride(PEACl) molecules as a buffer layer to modify the buried interface of p-i-n structured PSCs,aiming to enhance the uniformity of self-assembled monolayers(SAMs) and facilitate the uniform nucleation and growth of perovskite films on the substrate. Furthermore, the introduction of the PEACl buffer layer effectively passivates defects at the bottom of the perovskite layer and notably enhances the crystal quality of the perovskite film by mitigating residual stress,thereby reducing nonradiative recombination loss. Following these optimizations, the MA-free PSCs treated with PEACl achieve a power conversion efficiency(PCE) of 24.11%, with significant improvements in storage, thermal stability, and operational stability. Particularly noteworthy is the device's performance in an unencapsulated state, whereas after 1,500 hours of continuous light operation stability testing, it retains 97% of its original efficiency. This study not only enriches the systematic understanding of the characteristics of the buried interface in PSCs but also contributes significantly to advancing the commercial production of perovskite photovoltaic technology.

关键词： defect-induced recombination buried interfaces inverted perovskite solar cells crystallization lattice mismatch

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Interfacial Zn2+-solvation regulator towards reversible and stable Zn anode

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Journal of Energy Chemistry 2025年第1期100卷 684-692页

作者： Miao Zhou Xiongbin Luo Hang Li Shan Guo Zhuang Tong Xiaotao Zhou Xu Li Zhaohui Hou Shuquan liang Guozhao Fang College of Mechanical Engineering Key Laboratory of Hunan Province for Advanced Carbon-based Functional Materials Hunan Institute of Science and Technology School of Materials Science and Engineering Key Laboratory of Electronic Packaging and Advanced Functional Materials of Hunan Province Central South University College of Materials and Metallurgy Guizhou University national Energy Metal Resources and new Materials Key Laboratory Central South University

Aqueous zinc-ion batteries （AZIBs） are fundamentally challenged by the instability of the electrode/electrolyte interface,predominantly due to irreversible zinc （Zn） deposition and hydrogen ***,the intricate mechanisms behind the electrochemical discrepancies induced by interfacial Zn2+-solvation and deposition behavior demand comprehensive *** molecules endowed with special functional groups （such as hydroxyl,carboxyl,etc.） have the potential to significantly optimize the solvation structure of Zn2+and regulate the interfacial electric double layer （EDL）.By increasing nucleation overpotential and decreasing interfacial free energy,these functional groups facilitate a lower critical nucleation radius,thereby forming an asymptotic nucleation model to promote uniform Zn ***,this study presents a pioneering approach by introducing trace amounts of n-butanol as solvation regulators to engineer the homogenized Zn （H-Zn） anode with a uniform and dense *** interfacial reaction and structure evolution are explored by in/ex-situ experimental techniques,indicating that the H-Zn anode exhibits dendrite-free growth,no by-products,and weak hydrogen evolution,in sharp contrast to the bare ***,the H-Zn anode achieves a remarkable Zn utilization rate of approximately 20% and simultaneously sustains a prolonged cycle life exceeding 500 ***,the H-Zn//nH4V4O10（nVO） full battery showcases exceptional cycle stability,retaining 95.04%capacity retention after 400 cycles at a large current density of 5 A *** study enlightens solvation-regulated additives to develop Zn anode with superior utilization efficiency and extended operational lifespan.

关键词： Solvation

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Co@C-n as an electronic mediator anchored with Cu2O nanoparticles enables efficient photoreduction of CO2 to CO with nearly 100% selectivity

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Science China Chemistry 2025年

作者： Xingbin Pan Xiuzheng Deng Jingshan Fan Jiangchuan Liu Changhai Liu Zhongyu Li Qian liang Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology CNPC-CZU Innovation Alliance School of Petrochemical Engineering Changzhou University School of Materials Science & Engineering Changzhou University

Solar-driven CO2conversion into value-added chemical provides an attractive strategy for sustainable development. However,the enhanced CO2photoreduction performance with target product selectivity remains a major challenge. Here, we develop a novel strategy involving Cu2O nanoparticles in situ grown on the surface of ZIF-67-derived Co@C-n nanocages （CC） to create abundant active sites and appropriate heterointerfaces. A remarkable CO selectivity of 95.7%with a yield of 117.39μmol g-1h-1and an apparent quantum efficiency as high as 1.88%at 420 nm was obtained over CC-60 catalyst in pure water, which was 87.6times higher than that of pure Cu2O. Theoretical calculations and experiments indicated that Co@C-n nanocages as charge mediator not only rapidly trap photogenerated electrons to promote charge separation efficiency, but also regulate the d-band center of Cu atoms to move to the Fermi energy level, thereby optimizing the reaction kinetics to facilitate the highly selective conversion of the key intermediate *CO desorption to CO.

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Laser assisted phase transformation of carbon-based transition metal oxide electrode for high-performance supercapacitor application

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Science China Chemistry 2025年

作者： Mingzhen Xiu Jianghong Zhang Yu Lu Xun Cao Kang Huang Siyu Zhu Bowei Zhang Yu liang Chunwang Zhao Junsheng Wu Yizhong Huang School of Materials Science and Engineering Nanyang Technological University Energy Research Institute Interdisciplinary Graduate Programme Nanyang Technological University Institute of Sustainability for Chemicals Energy and Environment Agency for Science Technology and ResearchSingapore Institute of Advanced Materials and Technology University of Science and Technology Beijing School of Materials Science and Technology Shenyang University of Chemical Technology School of Materials Science and Hydrogen Energy Foshan University

Transitional metal oxides have a wide range of applications due to their superior *** enhanced performance of metal oxide relies on their desirable oxidation states,which is challenging to achieve and requires complex *** study demonstrates a facile strategy enabling rapid phase transformation of transition metal *** approach involves synthesis of a tetragonal Mn3O4/carbon cloth composite using the liquid plasma discharge deposition （LPDD） technique,followed by laser irradiation with the presence of ethylene glycol under an n2gas *** resulting face-centered cubic MnO/carbon cloth electrode exhibits an excellent capacitance of 1,125 F g-1at 2 A g-1,with remarkable capacitance retention of 95%after10,000 *** approach can be extended to other transition metals including Co,Cu,Cr,Fe,ni,and *** simulations reveal the significance of ethylene glycol and the underlying mechanism associated with the phase transformation of transition metal *** present study offers a powerful technique for the phase transformation of transition metal oxide which can guide the development of new electrode materials with enhanced electrochemical properties for high-performance energy storage applications.

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Preparation of click-driven cross-linked anion exchange membranes with low water uptake

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Particuology 2020年第1期18卷 65-73页

作者： Abhishek n.Mondal Jianqiu Hou Yubin He liang Wu liang Ge Tongwen Xu CAS Key Laboratory of Soft Matter Chemistry Collaborative Innovation Center of Chemistry for Energy MaterialsSchool of Chemistry and Material ScienceUniversity of Science and Technology of ChinaHefei 230026China

Significant advancement in anion exchange membrane(AEM)fuel cell(AEMFC)technology is important in the field of renewable *** with comb-shaped architectures have attracted considerable research interest because of some unique features,including high anion conductivity,low swelling,and high alkaline ***,we report preparation,characterization,and performance evaluation of a novel comb-shaped cross-linked AEM synthesized by the thiol-ene click and Menshutkin *** prepared ionomer decreases the trade-off between the water uptake and the *** thiol-ene click reaction was used to synthesize the 1,14-di(1H-imidazol-1-yl)-6,9-dioxa-3,12-dithiatetradecane(IDDT)*** was then introduced into the brominated poly(2,6-dimethyl-1,4-phenylene oxide)backbone by the Menshutkin *** prepared ionomers show high thermomechanical stability,which is needed in AEMFC *** CLInK-15-100 membrane(ion exchange capacity 1.23 mmol/g)shows relatively good conductivities of 19.66 and 34.91 mS/cm at 30 and 60℃,***,the membrane shows water uptake of only 14.22%at room temperature,which is considerably lower than many previously reported *** 16 days of alkaline treatment in 1 M naOH solution at 60℃,the CLInK-15-100 membrane retains 77%of its initial conductivity,which is much better than the traditional quaternized poly(2,6-dimethyl-1,4-phenylene oxide)membrane.

关键词： Anion exchange membrane Fuel cell Thiol-ene click reaction Water uptake Comb-shaped architecture

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Layered SnS sodium ion battery anodes synthesized near room temperature

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nano Research 2017年第12期10卷 4368-4377页

作者： Chuan Xia Fan Zhang Hanfeng liang Husam n. Alshareef Materials Science and Engineering King Abdullah University of Science and Technology (KAUST) Thuwa123955-6900 Saudi Arabia

In this report, we demonstrate a simple chemical bath deposition approach for the synthesis of layered SnS nanosheets （typically 6 nm or -10 layers thick） at very low temperature （40℃）. We successfully synthesized SnS/C hybrid electrodes using a solution-based carbon precursor coating with subsequent carbonization strategy. Our data showed that the ultrathin carbon shell was critical to the cycling stability of the SnS electrodes. As a result, the as-prepared binder-free SnS/C electrodes showed excellent performance as sodium ion battery anodes. Specifically, the SnS/C anodes delivered a reversible capacity as high as 792 mAh-g-1 after 100 cycles at a current density of 100 mA·g-1 They also had superior rate capability （431 mAh.g-1 at 3,000 mA.g-1） and stable long-term cycling performance under a high current density （345 mAh-g-1 after 500 cycles at 3 A.g-1）. Our approach opens up a new route to synthesize SnS-based hybrid materials at low temperatures for energy storage and other applications. Our process will be particularly useful for chalcogenide matrix materials that are sensitive to high temperatures during solution synthesis.

关键词： SnS sodium ion battery anode one-step synthesis

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Torsional mechanics of single walled carbon nanotubes with hydrogen for energy storage and fuel cell applications

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Science China(Physics,Mechanics & Astronomy) 2019年第3期62卷 93-101页

作者： V.Vijayaraghavan J.F.n.Dethan liang Gao School of Mechanical and Manufacturing Engineering University of New South Wales School of Engineering Monash University Malaysia State Key Laboratory for Digital Manufacturing Equipment and Technology Huazhong University of Science and Technology

Torsional mechanics of single walled carbon nanotubes(SWCnTs) encapsulated with hydrogen molecules was investigated in this study, using the molecular dynamics(MD) simulation approach. The torsional properties of hydrogen stored SWCnTs were crucial for determining the durability and lifetime of SWnCTs-based energy storage and proton exchange membrane fuel cell(PEMFC) applications. The influence of hydrogen storage concentration, SWCnT geometry, vacancy defects, temperature variation and varying boundaries of rotated as well as fixed groups on the torsional mechanics of SWCnT was investigated. The results and conclusions provide an insight into the torsional properties of SWCnTs with hydrogen storage that could be used for the development of SWCnTs-based hydrogen storage devices and PEMFC applications.

关键词： single walled carbon nanotubes torsional properties hydrogen molecules vacancy defects

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Synthesis of chiral phosphine derivatives through a copper（I）-catalyzed desymmetric SnAr reaction

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Science China Chemistry 2025年

作者： Shuai Zhang Pei-Zhi Liu Yan-Bo Li Qi Zhang Jun-Zhao Xiao Yi-Fan Wang Tian-Yu Wei Jia-Wei Jiang Ye Wang Qian Peng liang Yin Key Laboratory of Fluorine and nitrogen Chemistry and Advanced Materials Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences Chinese Academy of Sciences State Key Laboratory of Elemento-Organic Chemistry and Tianjin Key Laboratory of Biosensing and Molecular Recognition College of Chemistry Frontiers Science Center for New Organic Matter Nankai University Haihe Laboratory of Sustainable Chemical Transformations

Axially chiral phosphines are a class of extremely important ligands in asymmetric catalysis. Herein, an unprecedented copper（I）-catalyzed asymmetric SnAr reaction with HP（S）R2is uncovered, which delivers a series of axially chiral phosphine derivatives in high yields with excellent enantioselectivity. Furthermore, the diastereoselective reaction with the kinetic resolution of racemic HP（S）ArR proceeds smoothly, providing the products with moderate diastereoselectivity and excellent enantioselectivity. Control experiments indicate that HP（S）Ph2is much more active than HPPh2and HP（O）Ph2as the pronucleophile in the present reaction. It is found that the SnAr reaction （the first SnAr） proceeds in a desymmetric manner, providing the desired chiral products while a continued SnAr reaction （the second SnAr） slightly occurs in a kinetic resolution manner in the present catalytic system, which enhances the ee of the desired chiral products. DFTcalculations support a concerted reaction pathway rather than a step-wise mechanism. Finally, axially chiral olefin-phosphines produced by the present method work as suitable ligands in Pdcatalyzed asymmetric allylic substitution with C-, n-, and O-nucleophiles and Rh-catalyzed asymmetric addition of arylboronic acid to benzil.

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Study of viruses co-infecting white clover(Trifolium repens)in China

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Journal of Integrative Agriculture 2017年第9期16卷 1990-1998页

作者： liang Qiao-lan WEI Lie-xin XU Bing-liang A.Calderón-Urrea XIAnG Dong College of Plant Protection Gansu Agricultural UniversityLanzhou 730070P.R.China Biocontrol Engineering Laboratory of Crop Diseases and Pests of Gansu Province Lanzhou 730070P.R.China Department of Biology California State UniversityFresnoCA 93740USA

Globally, white clover（Trifolium repens L.） is commonly infected by plant viruses. It is grown at gardens, roadsides, and public areas as ornamental plants in northern China. Some leaves present disease symptoms that are similar to those of virus infection. However, to our knowledge, no records are available from China regarding white clover（Trifolium repens L.） virus co-infection. To determine the viral species that infect white clover in China, plant samples with virus disease symptoms were collected and virion morphology and ultrastructure morphology of co-infected plants were observed by electron microscopy; viruses were detected by enzyme linked immunosorbent assay（ELISA） and reverse transcription PCR（RT-PCR）. Virus co-infection was studied by double antibody sandwich enzyme linked immunosorbent assay（DAS-ELISA） and real-time fluorescence quantitative PCR（RT-q PCR） after rub-inoculation of virus-free white clover planted in a growth chamber（25°C） with a photoperiod of 16 h, using single or several purified virions. Results showed that there were six types of symptoms, including those of shrinking mosaic, shrinking and macular mosaic, severe mottle mosaic, yellow macular mosaic, shrinkage chlorisis, and ring plaque and ring stria. The incidence rates for each symptom were 20.93, 1.48, 16.85, 59.07, 1.30, and 0.37%, respectively, based on the field investigation. Two types of viral pathogens were identified as Alfalfa mosaic virus（AMV） and White clover mosaic virus（WCMV）. In mesophyll cells, virus particles with bacilliform virions formed aggregates and linear virions were bundle shaped. The detection rate of AMV was 100% in white clover samples by DAS-ELISA and RT-PCR detection, whereas that of WCMV was 83.33%. The co-infection rate was 83.33%. The relative contents of AMV and WCMV were significantly increased by 5.897-and 3.515-fold upon co-infection, when compared to that with single virus infection. We observed larger starch particles and fewer or collapsed c

关键词： clover AMV WCMV viral co-infection virus-induced pathological changes DAS-ELISA RT-PCR RT-qPCR

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