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A review:Multi-hierarchy design strategy of electrocatalysts for energy molecule conversion
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作者 Chenjia Liang Rurong Liu +6 位作者 Ruiyao zhao Xiaoxia Hou yingxuan zhao Jie Yang Tao Wang Teng Chen Weiping Ding 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第11期54-68,I0003,共16页
Under the new energy resource structure,electrocatalysts are key materials for the development of proton membrane fuel cells,electrolysis of aquatic hydrogen devices,and carbon dioxide reduction equipment,to address e... Under the new energy resource structure,electrocatalysts are key materials for the development of proton membrane fuel cells,electrolysis of aquatic hydrogen devices,and carbon dioxide reduction equipment,to address energy shortages and even environmental pollution issues.Although controlling the morphology or doping with heteroatoms for catalyst active centers have accelerated the reaction rate,it is difficult to solve the problems of multiple by-products,and poor stability of catalytic sites.From this,it will be seen that single regulation of metal active centers is difficult to comprehensively solve application problems.Orderly assembly and coordination of catalyst multi-hierarchy structures at the mesoscale above the nanometer level probably be more reasonable strategies,and numerous studies in thermal catalysis have supported this viewpoint.This article reviews the multi-hierarchy design of electrocatalyst active centers,high-energy supports,and peripheral structures in recent years,providing unconventional inspiration about electrocatalyst creation,which perhaps serves as a simple tutorial of electrocatalysis exploration for abecedarian. 展开更多
关键词 Novel electrocatalysts Energy molecular conversion Multi-hierarchy design strategy
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Stepwise Fabrication of Co-Embedded Porous Multichannel Carbon Nanofibers for High-Efficiency Oxygen Reduction 被引量:3
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作者 Zeming Tang yingxuan zhao +2 位作者 Qingxue Lai Jia Zhong Yanyu Liang 《Nano-Micro Letters》 SCIE EI CAS CSCD 2019年第2期206-216,共11页
A novel nonprecious metal material consisting of Coembedded porous interconnected multichannel carbon nanofibers(Co/IMCCNFs) was rationally designed for oxygen reduction reaction(ORR)electrocatalysis.In the synthesis,... A novel nonprecious metal material consisting of Coembedded porous interconnected multichannel carbon nanofibers(Co/IMCCNFs) was rationally designed for oxygen reduction reaction(ORR)electrocatalysis.In the synthesis,ZnCo2O4 was employed to form interconnected mesoporous channels and provide highly active Co3O4/Co core–shell nanoparticle-based sites for the ORR.The IMC structure with a large synergistic effect of the N and Co active sites provided fast ORR electrocatalysis kinetics.The Co/IMCCNFs exhibited a high half-wave potential of 0.82 V(vs.reversible hydrogen electrode) and excellent stability with a current retention up to 88% after 12,000 cycles in a current–time test,which is only 55% for 30 wt% Pt/C. 展开更多
关键词 Nonprecious metal material MULTICHANNEL carbon NANOFIBER Oxygen reduction reaction Core–shell NANOPARTICLE SYNERGISTIC effect
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FeCl_3模板辅助法由质子盐制备氮、硫、铁三掺杂碳纳米片及其催化氧还原反应(英文) 被引量:1
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作者 朱军杰 来庆学 +2 位作者 赵颖轩 钟佳 梁彦瑜 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2018年第9期1453-1462,共10页
作为一种新型能源技术,燃料电池具有能源转化效率高、燃料可再生、运行安全清洁等优点,因而在应对全球持续增长的能源、环境问题方面受到广泛的研究.但是,燃料电池的阴极氧还原反应(ORR)存在动力学缓慢的固有特性,其反应过电位高,需要... 作为一种新型能源技术,燃料电池具有能源转化效率高、燃料可再生、运行安全清洁等优点,因而在应对全球持续增长的能源、环境问题方面受到广泛的研究.但是,燃料电池的阴极氧还原反应(ORR)存在动力学缓慢的固有特性,其反应过电位高,需要在催化剂的辅助下才能顺利发生反应并提供足够的电极电势.目前ORR催化性能最优的是铂基催化剂,但其存在着资源稀缺、价格昂贵、循环寿命差等缺陷,这也是制约燃料电池商业化应用的主要因素.因而要想实现燃料电池的大规模应用,寻找新的可替代铂基催化剂、且储量丰富、价格低廉的优秀ORR催化剂成为了研究的热点.近几年来,杂原子掺杂的碳材料以其价格低、催化性能卓越、优异的稳定性和抗甲醇性能等优点,逐渐发展成为最有前景的ORR催化剂.本文以FeCl_3为模板和铁源,质子盐对苯二胺(PPS)为碳、氮、硫源,采用简单的一步中和法制备氮、硫、铁三掺杂的二维介孔碳纳米片催化剂(NSFC).TEM和BET结果显示,Fe Cl3不仅起到了二维模板的作用,同时在热处理过程中与无定形碳发生作用形成了丰富的介孔,大大提高了材料的比表面积和结构开放性,为ORR反应提供了反应场所.XPS结果显示,质子盐中和合成法不仅有效地简化了NSFC的合成步骤,而且能够灵活地控制材料的元素组成,实现了氮和硫的原位掺杂,有效构筑了杂原子掺杂活性位;同时FeCl_3也为催化剂材料引入了Fe元素,进而形成催化活性更加优异的Fe-Nx活性位.电化学测试结果表明,通过调整FeC l3和PPS的比例,NSFC-3催化剂材料在结构形貌和表面功能达到了同时最优化,获得了与商业30 wt%Pt/C可比的催化性能,其起始电位和极限电流密度分别达到了–0.03 V和5.05 mA/cm2,同时NSFC-3具有优于商业30wt%Pt/C的催化选择性、稳定性和抗甲醇性能.这源于稳定的二维纳米片层结构、丰富的表面介孔结构、大的比表面积和活性位点暴露率以及多种催化活性位点的协同催化效应. 展开更多
关键词 氧还原催化剂 FeCl3模板 质子盐 原位掺杂 协同催化
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Efficient silicon integrated four-mode edge coupler for few-mode fiber coupling
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作者 朱俊波 黄海阳 +3 位作者 赵瑛璇 李杨 盛振 甘甫烷 《Chinese Optics Letters》 SCIE EI CAS CSCD 2022年第1期54-59,共6页
Here,we designed a broadband,low loss,compact,and fabrication-tolerant silicon-based four-mode edge coupler,composed of a 1×3 adiabatic mode-evolution counter-taper splitter and a triple-tip inverse taper.Based o... Here,we designed a broadband,low loss,compact,and fabrication-tolerant silicon-based four-mode edge coupler,composed of a 1×3 adiabatic mode-evolution counter-taper splitter and a triple-tip inverse taper.Based on mode conversion and power splitting,the proposed structure can simultaneously realize efficient mode coupling from TE_(0),TM_(0),TE_(1),and TM_(1) modes of multimode silicon waveguides to linearly polarized(LP),LP^(01,x),LP_(01,y),LP_(11a,x),and LP_(11a,y),modes in the few-mode fiber.To the best of our knowledge,we proposed the first scheme of four LP modes coupling,which is fully compatible with standard fabrication process.The 3D finite-difference time-domain simulation results show that the on-chip conversion losses of the four modes remain lower than 0.62 dB over the 200 nm wavelength range,and total coupling losses are 4.1 dB,5.1 dB,2.1 dB,and 2.9 dB for TE_(0)-to-LP_(01,x),TM_(0)-to-LP_(01,y),TE_(1)-to-LP_(11a,x),and TM_(1)-to-LP_(11a,y),respectively.Good fabrication tolerance and relaxed critical dimensions make the four-mode edge coupler compatible with standard fabrication process of commercial silicon photonic foundries. 展开更多
关键词 multimode coupling CMOS compatibility silicon waveguide few-mode fiber
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