|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Attempted preparation of La_(0.5)Ba_(0.5)MnO_(3-δ) leading to an in-situ formation of manganate nanocomposites as a cathode for proton-conducting solid oxide fuel cells显示文摘A La_(0.5)Ba_(0.5)MnO_(3-δ) oxide was prepared using the sol-gel technique.Instead of a pure phase,La_(0.5)Ba_(0.5)MnO_(3-δ) was discovered to be a combination of La_(0.7)Ba_(0.3)MnO_(3-δ) and BaMnO_(3).The in-situ production of La_(0.7)Ba_(0.3)MnO_(3-δ)+BaMnO_(3) nanocomposites enhanced the oxygen vacancy(Vo)formation compared to single-phase La_(0.7)Ba_(0.3)MnO_(3-δ) or BaMnO_(3),providing potential benefits as a cathode for fuel cells.Subsequently,La_(0.7)Ba_(0.3)MnO_(3-δ)+BaMnO_(3) nanocomposites were utilized as the cathode for proton-conducting solid oxide fuel cells(H-SOFCs),which significantly improved cell performance.At 700 C,H-SOFC with a La_(0.7)Ba_(0.3)MnO_(3-δ)+BaMnO_(3) nanocomposite cathode achieved the highest power density(1504 mW·cm^(-2))yet recorded for H-SOFCs with manganate cathodes.This performance was much greater than that of single-phase La_(0.7)Ba_(0.3)MnO_(3-δ)or BaMnO_(3) cathode cells.In addition,the cell demonstrated excellent working stability.First-principles calculations indicated that the La_(0.7)Ba_(0.3)MnO_(3-δ)/BaMnO_(3) interface was crucial for the enhanced cathode performance.The oxygen reduction reaction(ORR)free energy barrier was significantly lower at the La_(0.7)Ba_(0.3)MnO_(3-δ)/BaMnO_(3) interface than that at the La_(0.7)Ba_(0.3)MnO_(3-δ) or BaMnO_(3) surfaces,which explained the origin of high performance and gave a guide for the construction of novel cathodes for H-SOFCs. | Rui Zhou Yanru Yin Hailu Dai Xuan Yang Yueyuan Gu Lei Bi | 2023 | Journal of Advanced Ceramics2023，12，6： | 1 |
| 2 | Study of shear transfer in A1/epoxy joint by digital photoelasticity显示文摘 | Lei Zhenkun Yun Hai Zhao Yanru | 2009 | Optics and Lasers in Engineering2009，47，6： | 1 |
| 3 | Tailoring cobalt-free La_(0.5)Sr_(0.5)FeO_(3-δ)cathode with a nonmetal cation-doping strategy for high-performance proton-conducting solid oxide fuel cells显示文摘A nonmetal doping strategy was exploited for the conventional La_(0.5)Sr_(0.5)FeO_(3-δ)(LSF)cathode,allowing high performance for proton-conducting solid oxide fuel cells(H-SOFCs).Unlike previous studies focusing on the utilization of metal oxides as dopants,phosphorus,which is a nonmetal element,was used as the cation dopant for LSF by partially replacing Fe ions to form the new La_(0.5)Sr_(0.5)Fe_(0.9)P_(0.1)O_(3-δ)(LSFP)compound.The H-SOFC using the LSFP cathode showed a two-fold peak power density as compared to that using the LSF cathode.Both experimental studies and first-principle calculations were used to unveil the mechanisms for the high performance of the LSFP cells. | Yanru Yin Hailu Dai Shoufu Yu Lei Bi Enrico Traversa | 2022 | SusMat2022，2，5： | 1 |
| 4 | Taking advantage of Li-evaporation in LiCoO_(2) as cathode for proton-conducting solid oxide fuel cells显示文摘LiCoO_(2),a widely used electrode material for Li-ion batteries,was found to be suitable as a cathode material for proton-conducting solid oxide fuel cells(H-SOFCs).Although the evaporation of Li in LiCoO_(2) was detrimental to the Li-ion battery performance,the Li-evaporation was found to be beneficial for the H-SOFCs.The partial evaporation of Li in the LiCoO_(2) material preparation procedure led to the in-situ formation of the LiCoO_(2)+Co_(3)O_(4) composite.Compared to the cell using the pure phase LiCoO_(2) cathode that only generated moderate fuel cell performance,the H-SOFCs using the LiCoO_(2)+Co_(3)O_(4) cathode showed a high fuel cell performance of 1160 mW·cm^(-2) at 700℃,suggesting that the formation of Co_(3)O_(4) was critical for enhancing the performance of the LiCoO_(2) cathode.The first-principles calculation gave insights into the performance improvements,indicating that the in-situ formation of Co_(3)O_(4) due to the Li-evaporation in LiCoO_(2) could dramatically decrease the formation energy of oxygen vacancies that is essential for the high cathode performance.The evaporation of Li in LiCoO_(2),which is regarded as a drawback for the Li-ion batteries,is demonstrated to be advantageous for the H-SOFCs,offering new selections of cathode candidates for the H-SOFCs. | Yangsen XU Shoufu YU Yanru YIN Lei BI | 2022 | Journal of Advanced Ceramics2022，11，12： | 1 |
| 5 | Study of shear transfer in Al/epoxy joint bydigital photoelasticity 显示文摘 | Lei Zhenkun Yun Hai Zhao Yanru XingYongming Pan Xuemin | 2009 | Optics and Lasers inEngineering2009，47，6： | 1 |
| 6 | Successful preparation of BaCo_(0.5)Fe_(0.5)O_(3–δ)cathode oxide by rapidly cooling allowing for high-performance proton-conducting solid oxide fuel cells显示文摘A pure phase BaCo_(0.5)Fe_(0.5)O_(3–δ)(BCF),which cannot be obtained before,is successfully prepared in this study by using the calcination method with a rapid cooling procedure.The successful preparation of BCF allows the evaluation of this material as a cathode for proton-conducting solid oxide fuel cells(H-SOFCs)for the first time.An H-SOFC using the BCF cathode achieves an encouraging fuel cell performance of 2012 mW·cm–2 at 700,two℃-fold higher than that of a similar cell using the classical high-performance Ba_(0.5)Sr_(0.5)Co_(0.8)Fe_(0.2)O_(3–δ)(BSCF)cathode.First-principles calculations reveal the mechanism for the performance enhancement,indicating that the new BCF cathode significantly lowers the energy barriers in the oxygen reduction reaction(ORR)compared with the BSCF cathode.Therefore,improved cathode performance and fuel cell output are obtained for the BCF cell.The fuel cell using the BCF cathode also shows excellent long-term stability that can work stably for nearly 900 h without noticeable degradations.The fuel cell performance and long-term stability of the current BCF cell are superior to most of the H-SOFCs reported in previous reports,suggesting that BCF is a promising cathode for H-SOFCs. | Yanru Yin Yanbin Zhou Yueyuan Gu Lei Bi | 2023 | Journal of Advanced Ceramics2023，12，3： | 1 |
| 7 | Exotic Plant Alnus trabeculosa Alters the Composition and Diversity of Native Rhizosphere Bacterial Communities of Phragmites australis显示文摘Alnus trabeculosa, a rhizobia-nodulating tree, was introduced into the Chongxi tidal wetland in the Yangtze River estuary of China to increase the biodiversity of plants and restore tidal wetland functions. However, the effect of the introduced plant on soil bacterial communities and restoration outcomes remains unknown. In this study, the rhizosphere bacterial community structure and diversity were compared between Phragmites australis monospecific community and A. trabeculosa-P. australis mixed communities,aiming to assess whether A. trabeculosa influenced the rhizosphere bacterial communities of P. australis and to investigate whether different taxonomic groups within a soil community may respond similarly to the presence of an introduced exotic plant. Among the14 phylogenetic phyla detected, Proteobacteria and Acidobacteria were the dominant bacterial taxa in the rhizosphere. Phylogenetic analysis of the predominant Proteobacteria showed that the clones from the rhizosphere soils of A. trabeculosa and P. australis in A. trabeculosa-P. australis mixed communities were more diverse than those in the rhizosphere soil of P. australis in P. australis monospecific community. The rhizosphere community in the wetland potentially included active microbial community related to carbon, nitrogen, and sulfur cycling in the Yangtze River estuary. The rhizosphere soil of P. australis in A. trabeculosa-P. australis mixed communities exhibited the highest Shannon diversity index(H′) and Simpson diversity index(1/D)(H = 4.52, 1/D =253). Correspondence analyses revealed that the bacterial community structures were altered after A. trabeculosa was introduced. | CHEN Xueping ZHANG Xuanxuan ZHU Xi'e ZHANG Hui LIANG Xia LEI Yanru HE Chiquan | 2016 | Pedosphere2016，26，1： | 1 |
| 8 | Assessing the conservation impact of Chinese indigenous chicken populations between ex-situ and in-situ using genome-wide SNPs显示文摘Conservation programs require rigorous evaluation to ensure the preservation of genetic diversity and viability of conservation populations. In this study, we conducted a comparative analysis of two indigenous Chinese chicken breeds, Gushi and Xichuan black-bone, using whole-genome SNPs to understand their genetic diversity, track changes over time and population structure. The breeds were divided into five conservation populations(GS1, 2010, ex-situ;GS2, 2019, ex-situ;GS3, 2019, in-situ;XB1, 2010, in-situ;and XB2, 2019, in-situ) based on conservation methods and generations. The genetic diversity indices of three conservation populations of Gushi chicken showed consistent trends, with the GS3 population under in-situ strategy having the highest diversity and GS2 under ex-situ strategy having the lowest. The degree of inbreeding of GS2 was higher than that of GS1 and GS3. Conserved populations of Xichuan black-bone chicken showed no obvious changes in genetic diversity between XB1 and XB2. In terms of population structure, the GS3 population were stratified relative to GS1 and GS2. According to the conservation priority, GS3 had the highest contribution to the total gene and allelic diversity in GS breed, whereas the contribution of XB1 and XB2 were similar. We also observed that the genetic diversity of GS2 was lower than GS3, which were from the same generation but under different conservation programs(in-situ and ex-situ). While XB1 and XB2 had similar levels of genetic diversity. Overall, our findings suggested that the conservation programs performed in ex-situ could slow down the occurrence of inbreeding events, but could not entirely prevent the loss of genetic diversity when the conserved population size was small, while in-situ conservation populations with large population size could maintain a relative high level of genetic diversity. | Wenting Li Chaoqun Gao Zhao Cai Sensen Yan Yanru Lei Mengya Wei Guirong Sun Yadong Tian Kejun Wang Xiangtao Kang | 2024 | Journal of Integrative Agriculture2024，23，3： | 0 |
| 9 | Nonstoichiometric Yttrium Hydride–Promoted Reversible Hydrogen Storage in a Liquid Organic Hydrogen Carrier显示文摘N-Ethylcarbazole(NEC)is one of the most promising liquid organic hydrogen carriers(LOHCs),but its application is limited by sluggish kinetics due to lack of high-efficiency,low-cost catalysts.This work reports a cobalt(Co)-based catalyst promoted by nonstoichiometric yttrium hydride(YH_(3−x))to achieve high-efficiency,reversible hydrogen storage in NEC,with>5.5 wt%reversible hydrogen storage capacity could be achieved below 473 K,and with good kinetics.The YH_(3−x)-promoted Co-based catalyst is the first non-noble metal catalyst with high activity for NEC hydrogenation and 12H-NEC dehydrogenation reactions.A mechanistic study suggests that YH_(3−x)facilitates the reversible hydrogen transfer both in the hydrogenation and the dehydrogenation reactions.The nonstoichiometric YH_(3−x)contained both lattice H and H vacancies with tunable H chemical potential serve as the H donor and H acceptor for reversible hydrogen transfer.Our results support the practical application of LOHCs and inspire new approaches for the utilization of conventional metal hydrides to promote versatile H transfer reactions. | Yong Wu Yanru Guo Hongen Yu Xiaojing Jiang Yuxuan Zhang Yue Qi Kai Fu Lei Xie Guoling Li Jie Zheng Xingguo Li | 2021 | CCS Chemistry2021，3，3： | 0 |
| 10 | Trace ruthenium promoted dual-reconstruction of CoFeP@C/NF for activating overall water splitting performance beyond precious-metals显示文摘At present,Ru dopants mainly enhance electrocatalytic performance by inducing strain,vacancy,local electron difference,and synergy.Surprisingly,this work innovatively proposes that trace Ru atoms induce dual-reconstruction of phosphide by regulating the electronic configuration and proportion of Co–P/Co–O species,and ultimately activate superb electrocatalytic performance.Specifically,Ru-CoFeP@C/nickel foam(NF)is reconstructed to generate hydrophilic Co(OH)_(2)nanosheets during the hydrogen evolution reaction(HER)process,further accelerating the alkaline HER kinetics of phosphide.And the as-formed CoOOH during the oxygen evolution reaction(OER)process directly accelerates the oxygen overflow efficiency.As expected,the overpotential at 100 mA·cm^(−2)(η100)values of the reconstructed Ru-CoFeP@C/NF are 0.104 and 0.257 V for HER and OER,which are greatly lower than that of Pt/C-NF and RuO_(2)-NF benchmarks,respectively.This work provides guidance for the construction of highperformance catalysts for HER and OER dual reconstruction.This work provides a new idea for the optimization of catalyst structure and electrocatalytic performance. | Jinhong Ren Jie Liu Yunmei Du Shuangshuang Li Mengmeng Wang Bin Li Bo Yang Lei Wang Yanru Liu | 2023 | Nano Research2023，16，8： | 0 |
| 11 | Entropy engineering design of high-performing lithiated oxide cathodes for proton-conducting solid oxide fuel cells显示文摘A new medium entropy material LiCo_(0.25)Fe_(0.25)Mn_(0.2)5Ni_(0.2)5O_(2)(LCFMN)is proposed as a cathode for proton-conducting solid oxide fuel cells(H-SOFCs).Unlike traditional LiXO_(2)(X=Co,Fe,Mn,Ni)lithiated oxides,which have issues like phase impurity,poor chemical compatibility,or poor fuel cell performance,the new LCFMN material mitigates these problems,allowing for the successful preparation of pure phase LCFMN with good chemical and thermal compatibility to the electrolyte.Furthermore,the entropy engineering strategy is found to weaken the covalence bond between the metal and oxygen in the LCFMN lattice,favoring the creation of oxygen vacancies and increasing cathode activity.As a result,the H-SOFC with the LCFMN cathode achieves an unprecedented fuel cell output of 1803 mW·cm^(−2)at 700℃,the highest ever reported for H-SOFCs with lithiated oxide cathodes.In addition to high fuel cell performance,the LCFMN cathode permits stable fuel cell operation for more than 450 h without visible degradation,demonstrating that LCFMN is a suitable cathode choice for H-SOFCs that combining high performance and good stability. | Yufeng Li Yangsen Xu Yanru Yin Hailu Dai Yueyuan Gu Lei Bi | 2023 | Journal of Advanced Ceramics2023，12，11： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员