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铠甲催化剂助力锌-空气电池:氮掺杂石墨烯上超薄碳封装铁镍合金增强氧电催化
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作者 郭一博 薛圆媛 周震 《Chinese Journal of Catalysis》 SCIE CAS CSCD 2024年第3期206-215,共10页
改善氧还原反应(ORR)和氧析出反应(OER)的缓慢动力学对促进可充电锌-空气电池的应用具有重要意义.在过去十年中,研究人员致力于开发不含贵金属的双功能氧电催化剂,包括过渡金属(铁、钴、镍和锰)、合金、氧化物、氮化物、氢氧化物和磷化... 改善氧还原反应(ORR)和氧析出反应(OER)的缓慢动力学对促进可充电锌-空气电池的应用具有重要意义.在过去十年中,研究人员致力于开发不含贵金属的双功能氧电催化剂,包括过渡金属(铁、钴、镍和锰)、合金、氧化物、氮化物、氢氧化物和磷化物,以进一步降低催化剂的成本,并提高其性能.研究表明,铁基催化剂表现出较好的ORR催化活性,而镍基催化剂在OER方面具有出色的性能,因此将铁和镍进行合金化组合成为一种实现高效双功能催化活性的有效方法.然而,反复的氧化还原反应会导致金属在水溶液中溶解,从而使得催化剂的耐久性变差.因此,如何在保证催化活性的同时提升催化剂的耐久性,成为了科研人员面临的一项重大挑战.构建铠甲催化剂被证明是解决上述问题的一种有效策略.本文通过热解三聚氰胺、葡萄糖和无机金属盐组成的混合物,成功制备了一种极具前景的铠甲催化剂FeNi@NC,其由掺杂氮的类石墨烯纳米片上超薄碳壳封装的铁镍合金纳米颗粒构成.扫描电镜、透射电镜、能量色散光谱、X射线吸收光谱和X射线衍射系列表征结果证明了碳壳封装铁镍合金纳米颗粒的形成,X射线光电子能谱证明催化剂中铁镍合金的电子向外层碳壳转移.电化学测试结果表明,FeNi@NC的ORR起始电位和半波电位与商业Pt/C催化剂相当,并且OER性能也与商业RuO2催化剂相近,展现出了良好的双功能催化活性.理论计算结果表明,内部铁镍合金的电子向外层氮掺杂碳壳转移,不仅活化了碳表面,还显著提升了催化剂的ORR和OER活性.这种电子转移促进了铁镍合金与氮掺杂碳壳之间的强协同效应,共同赋予了催化剂出色的双功能催化能力.此外,包裹在FeNi合金纳米颗粒周围的碳壳不仅为催化剂提供了结构支撑,还显著增强了易溶解合金物质的稳定性和耐久性.在多次循环伏安测试后,FeNi@NC催化剂仍然能够维持较高的催化性能,循环后的电镜表征进一步证实了催化剂结构的稳定性.FeNi@NC催化剂的高效催化活性、界面上快速的物质和电荷传输以及稳定的封装结构,使其在作为可充电锌-空气电池正极时展现出高功率密度和长循环稳定性.综上,本文研究了杂原子掺杂碳材料负载限域生长过渡金属合金的可控制备及其电催化反应机制,为锌-空气电池提供了一种新的解决方案. 展开更多
关键词 锌-空气电池 铠甲催化剂 双功能电催化剂 FeNi合金 碳壳
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构筑高效耐腐蚀的碳铠甲层包覆Co_(9)Se_(8)电催化剂用于海水基锌空气电池
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作者 汪已萱 张灿辉 +5 位作者 汪兴坤 段嘉瑞 童科程 代水星 初蕾 黄明华 《物理化学学报》 SCIE CAS CSCD 北大核心 2024年第6期38-40,共3页
得益于较高的理论能量密度、环境友好性和丰富的海水储量,海水基锌-空气电池(S-ZABs)被认为是一种极具应用前景的储能和能源转换装置,是解决能源短缺和环境污染问题的能源装置之一。然而对于S-ZABs而言,构筑在海水中具有高耐氯离子腐蚀... 得益于较高的理论能量密度、环境友好性和丰富的海水储量,海水基锌-空气电池(S-ZABs)被认为是一种极具应用前景的储能和能源转换装置,是解决能源短缺和环境污染问题的能源装置之一。然而对于S-ZABs而言,构筑在海水中具有高耐氯离子腐蚀性与高性能的阴极氧还原反应电催化剂仍然具有挑战性。因此,我们通过高温硒化策略,在氮掺杂介孔碳材料上设计了超薄碳铠甲层封装的Co_(9)Se_(8)纳米颗粒高效ORR电催化剂(命名为NMC-Co_(9)Se_(8))。外部的超薄碳铠甲层不仅可以改善催化过程中的电子转移过程,抑制纳米颗粒的团聚,而且可以作为盔甲保护内部活性位点免受Cl^(-)吸附和腐蚀。得益于这种独特的结构,NMC-Co_(9)Se_(8)在0.1 mol·L^(-1)KOH海水电解质中表现出优异的ORR性能,其起始电位为0.904V,半波电位为0.860 V。更重要的是,基于NMC-Co_(9)Se_(8)催化剂的S-ZABs可提供172.4 m W·cm^(-2)的功率密度和超过150h的优异长期放电稳定性,均高于基于Pt/C的S-ZABs性能。这项工作为开发用于海水基锌-空气电池和其他能源转换技术具有耐氯离子腐蚀且高效的ORR催化剂提供了新思路。 展开更多
关键词 Co_(9)Se_(8)纳米颗粒 氧还原反应 超薄碳铠甲层 海水锌空气电池 耐氯离子腐蚀
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Efficient ORR catalysts for zinc-air battery: Biomass-derived ultra-stable Co nanoparticles wrapped with graphitic layers via optimizing electron transfer 被引量:5
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作者 Yu Feng Kexin Song +12 位作者 Wei Zhang Xinyan Zhou Seung Jo Yoo Jin-Gyu Kim Sifan Qiao Yugang Qi Xu Zou Zhongjun Chen Tingting Qin Nailin Yue Zizhun Wang Dabing Li Weitao Zheng 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2022年第7期211-218,I0006,共9页
The poor stability of non-noble metal catalysts in oxygen reduction reaction(ORR) is a main bottleneck that limits their big-scale application in metal-air batteries. Herein, we construct a chainmail catalyst(Co-NC-AD... The poor stability of non-noble metal catalysts in oxygen reduction reaction(ORR) is a main bottleneck that limits their big-scale application in metal-air batteries. Herein, we construct a chainmail catalyst(Co-NC-AD) with outstanding stability, via the competitive complexation and post absorption strategy,consisting of highly graphitic layers wrapped uniform-size Co nanoparticles(Co-NPs). Experiments combined with density functional theory(DFT) calculations jointly confirmed that the electron transfer occurred from the inner Co-NPs to the external graphitic layers. It facilitated the adsorption process of oxygen molecules and the hybridization of the O-2 p and C-1 p orbitals, which accelerated the ORR reaction kinetics. Consequently, our prepared Co-NC-AD shows excellent ORR activity, offered with a more positive initial potential(E_(onset)= 0.95 V) and half-wave potential(E_(1/2)= 0.86 V). The remarkable stability and resistance of methanol poisoning are merited from the protection effect of stable graphitic layers. In addition, the high electrochemical performance of Co-NC-AD-based zinc-air battery demonstrates their potential for practical applications. Therefore, our work provides new ideas for the design of nanoconfined catalysts with high stability and activity. 展开更多
关键词 chainmail catalyst Graphitic layers Co nanoparticles Oxygen reduction reaction
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Ultrathin oxygen-containing graphdiyne wrapping CoP for enhanced electrocatalytic hydrogen generation 被引量:2
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作者 Yan Lv Xueyan Wu +5 位作者 Hao Li Hongbo Zhang Jiaxin Li Zhiyou Zhou Jixi Guo Dianzeng Jia 《Nano Research》 SCIE EI CSCD 2023年第4期5073-5079,共7页
Graphdiyne(GDY)is fascinating in the construction of efficient and stable catalysts,but their performance is still somewhat restricted due to GDY’s thicker layers,as well as hydrophobic and relatively chemically iner... Graphdiyne(GDY)is fascinating in the construction of efficient and stable catalysts,but their performance is still somewhat restricted due to GDY’s thicker layers,as well as hydrophobic and relatively chemically inert surfaces.Herein,via oxidationexfoliation-reduction strategy,the self-supported electrode material of CoP nanosheets with ultrathin oxygen-containing GDY wrapping(CoP@RGDYO)for effective HER is constructed.The wrapping of ultrathin oxygen-containing GDY promotes charge transfer,improves the surface property,and enhances the acid and alkali resistance as well as the structural stability of the catalyst.As a result,CoP@RGDYO shows enhanced activity and stability in both acidic and alkaline media.Especially,it exhibits a low overpotential of 86 mV and exceptional stability under a 14000-cycle cyclic voltammetry scanning in alkaline media.This work provides new ideas for the design of GDY hybrid materials and the preparation of high-efficiency catalysts. 展开更多
关键词 graphdiyne chainmail catalyst HYDROPHILICITY stability hydrogen generation
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引入共价型氮化钒来提高氮掺杂碳的亲电性以促进氧还原反应 被引量:5
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作者 李士栋 庄泽超 +8 位作者 夏力学 朱杰鑫 刘子昂 贺汝涵 罗雯 黄文忠 石长玮 赵焱 周亮 《Science China Materials》 SCIE EI CAS CSCD 2023年第1期160-168,共9页
氮掺杂碳(NC)是一种有潜力的氧还原反应(ORR)电催化剂.氮掺杂碳可直接作为ORR活性位点中心,优化氮原子的电子结构对催化活性具有很大影响.本文通过简单的物理混合和煅烧处理,构建了一种由氮化钒(VN)纳米颗粒为核、“铠甲状”NC作为壳的... 氮掺杂碳(NC)是一种有潜力的氧还原反应(ORR)电催化剂.氮掺杂碳可直接作为ORR活性位点中心,优化氮原子的电子结构对催化活性具有很大影响.本文通过简单的物理混合和煅烧处理,构建了一种由氮化钒(VN)纳米颗粒为核、“铠甲状”NC作为壳的新型VN@NC纳米复合材料.得益于纳米线独特的核@壳结构和优化的电子结构,与纯NC和体相VN相比,所制备的VN@NC展现出更优异的ORR活性(起始电位:0.93 V).VN的引入诱导了电荷从NC上的氮原子转移到VN上的钒原子,增加了NC上氮原子的亲电性,从而优化了对含氧中间体的吸附过程.VN@NC也展现出了良好的循环稳定性(四万秒测试后,电流密度保持率为89%).本研究揭示了调节NC中氮原子电子结构的重要性,并为构建NC基复合型电催化剂提供了有效方法. 展开更多
关键词 亲电性 氧还原反应 电催化剂 氮化钒 物理混合 氮掺杂碳 壳结构 循环稳定性
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Highly efficient conversion of surplus electricity to hydrogen energy via polysulfides redox 被引量:1
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作者 Mo Zhang Jing Guan +2 位作者 Yunchuan Tu Suheng Wang Dehui Deng 《The Innovation》 2021年第3期103-108,共6页
Decoupled electrolysis of water is a promising strategy for peak load regulation of electricity.The key to developing this technology is to construct decoupled devices containing stable redox mediators and correspondi... Decoupled electrolysis of water is a promising strategy for peak load regulation of electricity.The key to developing this technology is to construct decoupled devices containing stable redox mediators and corresponding efficient catalysts,which remains a considerable challenge.Herein,we designed a high-performance device,using polysulfides as mediators and graphene-encapsulated CoNi as catalysts.It produced H2 with a low potential of 0.82 V at 100 mA/cm^(2),saving 60.2%more energy than direct water electrolysis.The capacity of H2 production reached 2.53105 mAh/cm^(2),which is the highest capacity reported so far.This device exhibited excellent cyclability in 15-day recycle tests,without any decay of performance.The calculation results revealed that the electronic structure of the graphene shell was modulated by the electron transfer from N-dopant and metal core,which significantly facilitated recycle of polysulfides on graphene surfaces.This study provides a promising method for constructing a smart grid by developing efficient decoupled devices. 展开更多
关键词 peak shaving and valley filling decoupled electrolysis H2 production chainmail catalyst polysulfides redox
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