Developing high efficient Pd-based electrocatalysts for oxygen reduction reaction(ORR) is still challenging for alkaline membrane fuel cell,since the strong oxygen adsorption energy and easy agglomerative intrinsic pr...Developing high efficient Pd-based electrocatalysts for oxygen reduction reaction(ORR) is still challenging for alkaline membrane fuel cell,since the strong oxygen adsorption energy and easy agglomerative intrinsic properties. In order to simultaneously solve these problems, Pd/Co_(3)O_(4)–N–C multidimensional materials with porous structures is designed as the ORR catalysts. In details, the ZIF-67 with polyhedral structure was firstly synthesized and then annealed at high-temperature to prepare the N-doped Co_(3)O_(4)carbon-based material, which was used to homogeneously confine Pd nanoparticles and obtained the Pd/Co_(3)O_(4)–N–C series catalysts. The formation of Co–N and C–N bond could provide efficient active sites for ORR. Simultaneously, the strong electronic interaction in the interface between the Pd and N-doped Co_(3)O_(4)could disperse and avoid the agglomeration of Pd nanoparticles and ensure the exposure of active sites, which is crucial to lower the energy barrier toward ORR and substantially enhance the ORR kinetics. Hence, the Pd/Co_(3)O_(4)–N–C nanocompounds exhibited excellent ORR catalytic performance, ideal Pd mass activity, and durability in 0.1 mol L-1KOH solution compared with Co_(3)O_(4)–N–C and Pd/C. The scalable synthesis method, relatively low cost, and excellent electrochemical ORR performance indicated that the obtained Pd/Co_(3)O_(4)–N–C electrocatalyst had the potential for application on fuel cells.展开更多
Enhancement of supercapacitors(SCs)with high-energy density and high-power density is still a great challenge.In this paper,a facile strategy for in situ anchoring of Co_(3)O_(4) particles on N doped carbon cloth(pCoN...Enhancement of supercapacitors(SCs)with high-energy density and high-power density is still a great challenge.In this paper,a facile strategy for in situ anchoring of Co_(3)O_(4) particles on N doped carbon cloth(pCoNCC)is reported.Due to the interaction of the doped N and Co_(3)O_(4),the electrochemical performance improves significantly,reaching 1,940.13 mF·cm^(−2) at 1 mA·cm^(−2) and energy density of 172.46μWh·cm^(−2) at the power density of 400μW·cm^(−2),much larger than that without N doping electrode of 28.5 mF·cm^(−2).An aqueous symmetric supercapacitor(ASSC)assembled by two pCoNCC electrodes achieves a maximum energy density of 447.42μWh·cm^(−2) and a highest power density of 8,000μW·cm^(−2).Utilizing such a high-energy storage ASSC,a digital watch and a temperature-humidity detector are powered for nearly 1 and 2 h,respectively.Moreover,the ASSC displays a superb electrochemical stability of 87.7%retention after 10,000 cycles at 40 mA·cm^(−2).This work would provide a new sight to enhance active materials performance and be beneficial for the future energy storage and supply systems.展开更多
Selective hydrogenation is an important industrial catalytic process in chemical upgrading, where Pd-based catalysts are widely used because of their high hydrogenation activities. However, poor selectivity and short ...Selective hydrogenation is an important industrial catalytic process in chemical upgrading, where Pd-based catalysts are widely used because of their high hydrogenation activities. However, poor selectivity and short catalyst lifetime because of heavy coke formation have been major concerns. In this work, atomically dispersed Pd atoms were successfully synthesized on graphitic carbon nitride （g-C3N4） using atomic layer deposition. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy （HAADF-STEM） confirmed the dominant presence of isolated Pd atoms without Pd nanoparticle （NP） formation. During selective hydrogenation of acetylene in excess ethylene, the g-C3N4-supported Pd NP catalysts had strikingly higher ethylene selectivities than the conventional Pd/Al2O3 and Pd/SiO2 catalysts. In-situ X-ray photoemission spectroscopy revealed that the considerable charge transfer from the Pd NPs to g-C3N4 likely plays an important role in the catalytic performance enhancement. More impressively, the single-atom Pd1/C3N4 catalyst exhibited both higher ethylene selectivity and higher coking resistance. Our work demonstrates that the single-atom Pd catalyst is a promising candidate for improving both selectivity and coking-resistance in hydrogenation reactions.展开更多
The preparation of highly active electrocatalysts with good durability and low cost for fuel cells is highly desir- able but still remains a significant challenge. Here we synthesized two dimensional （2D） C3N4 nanos...The preparation of highly active electrocatalysts with good durability and low cost for fuel cells is highly desir- able but still remains a significant challenge. Here we synthesized two dimensional （2D） C3N4 nanosheets supported palladium composites （C3N4/Pd） via a simple and convenient sonochemical approach. We have systematically stud- ied the electrocatalytic performance of as-prepared catalysts. We found that the prepared C3N4/Pd composites pos- sessed excellent catalytic activity and stability for oxygen reduction reaction （ORR） in alkaline media. Encourag- ingly, the C3N4/Pd catalysts exhibit the excellent electrocatalytic activity for methanol oxidation reaction （MOR） in alkaline media, even better than that of the commercial Pt/C catalyst, The excellent electrocatalytic performance of the 2D C3N4 nanosheets supported palladium composites catalysts results from their synergy effect between the ul- trathin substrate material with large surface area and excellent dispersion of palladium nanoparticles. This study demonstrates that sonochemical method opens up a new avenue for the preparation of electrocatalysts for fuel cells. We expect these materials are likely to find uses in a broad range of applications, for example, fuel cells, solar cells, batteries and other electrochemical analysis.展开更多
随着全球人口数量快速增长和科技不断进步,对能源需求逐步增加,但化石能源日渐枯竭,同时环境问题日趋严重.因此,亟需开发新型、绿色、高效的能源以及能源装置,以保障清洁能源的可持续利用.锂-氧电池因其能量密度高、环境友好等优点受到...随着全球人口数量快速增长和科技不断进步,对能源需求逐步增加,但化石能源日渐枯竭,同时环境问题日趋严重.因此,亟需开发新型、绿色、高效的能源以及能源装置,以保障清洁能源的可持续利用.锂-氧电池因其能量密度高、环境友好等优点受到了人们的广泛关注,并被认为是替代锂离子电池的新储能系统之一.然而,对于锂-氧电池仍需解决诸如能量密度低于理论值、倍率性能差和循环寿命短等难题.开发高效稳定的氧电极催化剂是解决上述问题的关键手段之一.在众多潜在的过渡金属氧化物催化剂中,四氧化三钴因其地壳丰度高、成本低和性能优异等优点成为研究热点.本文采用静电纺丝技术,结合热处理技术,成功制备了中空四氧化三钴纳米球镶嵌的多孔碳纳米纤维复合催化剂(H-Co_(3)O_(4)-CNFs),系统地研究了其氧还原反应(ORR)和析氧反应(OER)的电催化性能,以及作为锂-氧电池正极催化剂的电化学性能.结果表明,在碱性电解质中,H-Co_(3)O_(4)-CNFs具有较好的ORR/OER活性,展现出较好的双功能催化性能.H-Co_(3)O_(4)-CNFs作为锂-氧电池的氧电极催化剂材料,在100 mA g^(‒1)电流密度下的过电位为1.35 V,电池的放电比容量达到6134 mAh g^(‒1);当电流密度增加至800 mA g^(‒1)时,放电比容量仍能保持68.5%.在充放电电流密度为100 mA g^(‒1),限制容量为500 mAh g‒1的条件下,电池能保持150圈的稳定循环.H-Co3O4-CNFs催化剂较好的催化性能可归因于:(1)氮掺杂的多孔碳纤维具有良好的导电性和快速的电子传输能力;(2)多孔结构增大了电解液和催化剂活性位点的接触面积,并为放电产物过氧化锂的形成和分解提供了场所.另外,其良好的循环性能得益于裸露的Co_(3)O_(4)和嵌入纤维中的Co_(3)O_(4)形成的两种独立活性位点,这使其在ORR和OER过程中均有可用的催化活性位点,并在放电和充电过程中交替发挥作用.综上,本文研究结果为高效氧电极催化剂的设计提供了新思路。展开更多
基金funded by National Natural Science Foundation of China (21975129)Natural Science Foundation of Jiangsu Province (BK20190759)+1 种基金Nanjing Forestry UniversityPostgraduate Research & Practice Innovation Program of Jiangsu Province (SJCX21_0337)。
文摘Developing high efficient Pd-based electrocatalysts for oxygen reduction reaction(ORR) is still challenging for alkaline membrane fuel cell,since the strong oxygen adsorption energy and easy agglomerative intrinsic properties. In order to simultaneously solve these problems, Pd/Co_(3)O_(4)–N–C multidimensional materials with porous structures is designed as the ORR catalysts. In details, the ZIF-67 with polyhedral structure was firstly synthesized and then annealed at high-temperature to prepare the N-doped Co_(3)O_(4)carbon-based material, which was used to homogeneously confine Pd nanoparticles and obtained the Pd/Co_(3)O_(4)–N–C series catalysts. The formation of Co–N and C–N bond could provide efficient active sites for ORR. Simultaneously, the strong electronic interaction in the interface between the Pd and N-doped Co_(3)O_(4)could disperse and avoid the agglomeration of Pd nanoparticles and ensure the exposure of active sites, which is crucial to lower the energy barrier toward ORR and substantially enhance the ORR kinetics. Hence, the Pd/Co_(3)O_(4)–N–C nanocompounds exhibited excellent ORR catalytic performance, ideal Pd mass activity, and durability in 0.1 mol L-1KOH solution compared with Co_(3)O_(4)–N–C and Pd/C. The scalable synthesis method, relatively low cost, and excellent electrochemical ORR performance indicated that the obtained Pd/Co_(3)O_(4)–N–C electrocatalyst had the potential for application on fuel cells.
基金This work was supported by the National Natural Science Foundation of China(Nos.51772036 and 51572040)the Fundamental Research Funds for the Central Universities(Nos.2019CDXZWL001 and 2020CDCGJ005).
文摘Enhancement of supercapacitors(SCs)with high-energy density and high-power density is still a great challenge.In this paper,a facile strategy for in situ anchoring of Co_(3)O_(4) particles on N doped carbon cloth(pCoNCC)is reported.Due to the interaction of the doped N and Co_(3)O_(4),the electrochemical performance improves significantly,reaching 1,940.13 mF·cm^(−2) at 1 mA·cm^(−2) and energy density of 172.46μWh·cm^(−2) at the power density of 400μW·cm^(−2),much larger than that without N doping electrode of 28.5 mF·cm^(−2).An aqueous symmetric supercapacitor(ASSC)assembled by two pCoNCC electrodes achieves a maximum energy density of 447.42μWh·cm^(−2) and a highest power density of 8,000μW·cm^(−2).Utilizing such a high-energy storage ASSC,a digital watch and a temperature-humidity detector are powered for nearly 1 and 2 h,respectively.Moreover,the ASSC displays a superb electrochemical stability of 87.7%retention after 10,000 cycles at 40 mA·cm^(−2).This work would provide a new sight to enhance active materials performance and be beneficial for the future energy storage and supply systems.
基金Acknowledgements This work was supported by the Thousand Talents Plan, the National Natural Science Foundation of China （Nos. 21473169, 21673215, and 51402283）, the Fundamental Research Funds for the Central Universities （Nos. WK2060030017 and WK2060190026）, and the startup funds from the University of Science and Technology of China. This work was also supported by Hefei Science Center （No. 2015HSC-UP010）.
文摘Selective hydrogenation is an important industrial catalytic process in chemical upgrading, where Pd-based catalysts are widely used because of their high hydrogenation activities. However, poor selectivity and short catalyst lifetime because of heavy coke formation have been major concerns. In this work, atomically dispersed Pd atoms were successfully synthesized on graphitic carbon nitride （g-C3N4） using atomic layer deposition. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy （HAADF-STEM） confirmed the dominant presence of isolated Pd atoms without Pd nanoparticle （NP） formation. During selective hydrogenation of acetylene in excess ethylene, the g-C3N4-supported Pd NP catalysts had strikingly higher ethylene selectivities than the conventional Pd/Al2O3 and Pd/SiO2 catalysts. In-situ X-ray photoemission spectroscopy revealed that the considerable charge transfer from the Pd NPs to g-C3N4 likely plays an important role in the catalytic performance enhancement. More impressively, the single-atom Pd1/C3N4 catalyst exhibited both higher ethylene selectivity and higher coking resistance. Our work demonstrates that the single-atom Pd catalyst is a promising candidate for improving both selectivity and coking-resistance in hydrogenation reactions.
基金financially supported by the Key Research and Development Program of Hubei Province(2020BCA079)the National Natural Science Foundation of China(52173106)。
基金We greatly appreciate the support of the National Natural Science Foundation of China （Nos. 21475057, 21335004,） and the Program B tbr Outstanding PhD Candidates of Nanjing University. This work was also supported by the Program for New Century Excellent Talents in University （No. NCET-12-0256）.
文摘The preparation of highly active electrocatalysts with good durability and low cost for fuel cells is highly desir- able but still remains a significant challenge. Here we synthesized two dimensional （2D） C3N4 nanosheets supported palladium composites （C3N4/Pd） via a simple and convenient sonochemical approach. We have systematically stud- ied the electrocatalytic performance of as-prepared catalysts. We found that the prepared C3N4/Pd composites pos- sessed excellent catalytic activity and stability for oxygen reduction reaction （ORR） in alkaline media. Encourag- ingly, the C3N4/Pd catalysts exhibit the excellent electrocatalytic activity for methanol oxidation reaction （MOR） in alkaline media, even better than that of the commercial Pt/C catalyst, The excellent electrocatalytic performance of the 2D C3N4 nanosheets supported palladium composites catalysts results from their synergy effect between the ul- trathin substrate material with large surface area and excellent dispersion of palladium nanoparticles. This study demonstrates that sonochemical method opens up a new avenue for the preparation of electrocatalysts for fuel cells. We expect these materials are likely to find uses in a broad range of applications, for example, fuel cells, solar cells, batteries and other electrochemical analysis.
文摘随着全球人口数量快速增长和科技不断进步,对能源需求逐步增加,但化石能源日渐枯竭,同时环境问题日趋严重.因此,亟需开发新型、绿色、高效的能源以及能源装置,以保障清洁能源的可持续利用.锂-氧电池因其能量密度高、环境友好等优点受到了人们的广泛关注,并被认为是替代锂离子电池的新储能系统之一.然而,对于锂-氧电池仍需解决诸如能量密度低于理论值、倍率性能差和循环寿命短等难题.开发高效稳定的氧电极催化剂是解决上述问题的关键手段之一.在众多潜在的过渡金属氧化物催化剂中,四氧化三钴因其地壳丰度高、成本低和性能优异等优点成为研究热点.本文采用静电纺丝技术,结合热处理技术,成功制备了中空四氧化三钴纳米球镶嵌的多孔碳纳米纤维复合催化剂(H-Co_(3)O_(4)-CNFs),系统地研究了其氧还原反应(ORR)和析氧反应(OER)的电催化性能,以及作为锂-氧电池正极催化剂的电化学性能.结果表明,在碱性电解质中,H-Co_(3)O_(4)-CNFs具有较好的ORR/OER活性,展现出较好的双功能催化性能.H-Co_(3)O_(4)-CNFs作为锂-氧电池的氧电极催化剂材料,在100 mA g^(‒1)电流密度下的过电位为1.35 V,电池的放电比容量达到6134 mAh g^(‒1);当电流密度增加至800 mA g^(‒1)时,放电比容量仍能保持68.5%.在充放电电流密度为100 mA g^(‒1),限制容量为500 mAh g‒1的条件下,电池能保持150圈的稳定循环.H-Co3O4-CNFs催化剂较好的催化性能可归因于:(1)氮掺杂的多孔碳纤维具有良好的导电性和快速的电子传输能力;(2)多孔结构增大了电解液和催化剂活性位点的接触面积,并为放电产物过氧化锂的形成和分解提供了场所.另外,其良好的循环性能得益于裸露的Co_(3)O_(4)和嵌入纤维中的Co_(3)O_(4)形成的两种独立活性位点,这使其在ORR和OER过程中均有可用的催化活性位点,并在放电和充电过程中交替发挥作用.综上,本文研究结果为高效氧电极催化剂的设计提供了新思路。
