Dingsheng Wang

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Name: 王定胜; ,
Organization: Tsinghua University , China
Department: Department of Chemistry
Title: (PhD)
Co-reporter:Quanchen Feng, Shu Zhao, Yu Wang, Juncai Dong, Wenxing Chen, Dongsheng He, Dingsheng Wang, Jun Yang, Yuanmin Zhu, Hailiang Zhu, Lin Gu, Zhi Li, Yuxi Liu, Rong Yu, Jun Li, and Yadong Li
Journal of the American Chemical Society May 31, 2017 Volume 139(Issue 21) pp:7294-7294
Publication Date(Web):May 14, 2017
DOI:10.1021/jacs.7b01471
Improving the catalytic selectivity of Pd catalysts is of key importance for various industrial processes and remains a challenge so far. Given the unique properties of single-atom catalysts, isolating contiguous Pd atoms into a single-Pd site with another metal to form intermetallic structures is an effective way to endow Pd with high catalytic selectivity and to stabilize the single site with the intermetallic structures. Based on density functional theory modeling, we demonstrate that the (110) surface of Pm3̅m PdIn with single-atom Pd sites shows high selectivity for semihydrogenation of acetylene, whereas the (111) surface of P4/mmm Pd3In with Pd trimer sites shows low selectivity. This idea has been further validated by experimental results that intermetallic PdIn nanocrystals mainly exposing the (110) surface exhibit much higher selectivity for acetylene hydrogenation than Pd3In nanocrystals mainly exposing the (111) surface (92% vs 21% ethylene selectivity at 90 °C). This work provides insight for rational design of bimetallic metal catalysts with specific catalytic properties.
Co-reporter:Shufang Ji, Yuanjun Chen, Qiang Fu, Yifeng Chen, Juncai Dong, Wenxing Chen, Zhi Li, Yu Wang, Lin Gu, Wei He, Chen Chen, Qing Peng, Yu Huang, Xiangfeng Duan, Dingsheng Wang, Claudia Draxl, and Yadong Li
Journal of the American Chemical Society July 26, 2017 Volume 139(Issue 29) pp:9795-9795
Publication Date(Web):July 11, 2017
DOI:10.1021/jacs.7b05018
Here we report a novel approach to synthesize atomically dispersed uniform clusters via a cage-separated precursor preselection and pyrolysis strategy. To illustrate this strategy, well-defined Ru3(CO)12 was separated as a precursor by suitable molecular-scale cages of zeolitic imidazolate frameworks (ZIFs). After thermal treatment under confinement in the cages, uniform Ru3 clusters stabilized by nitrogen species (Ru3/CN) were obtained. Importantly, we found that Ru3/CN exhibits excellent catalytic activity (100% conversion), high chemoselectivity (100% for 2-aminobenzaldehyde), and significantly high turnover frequency (TOF) for oxidation of 2-aminobenzyl alcohol. The TOF of Ru3/CN (4320 h–1) is about 23 times higher than that of small-sized (ca. 2.5 nm) Ru particles (TOF = 184 h–1). This striking difference is attributed to a disparity in the interaction between Ru species and adsorbed reactants.
Co-reporter:Maolin Zhang, Yang-Gang Wang, Wenxing Chen, Juncai Dong, Lirong Zheng, Jun Luo, Jiawei Wan, Shubo Tian, Weng-Chon Cheong, Dingsheng Wang, and Yadong Li
Journal of the American Chemical Society August 16, 2017 Volume 139(Issue 32) pp:10976-10976
Publication Date(Web):July 31, 2017
DOI:10.1021/jacs.7b05372
Preparing metal single-atom materials is currently attracting tremendous attention and remains a significant challenge. Herein, we report a novel core–shell strategy to synthesize single-atom materials. In this strategy, metal hydroxides or oxides are coated with polymers, followed by high-temperature pyrolysis and acid leaching, metal single atoms are anchored on the inner wall of hollow nitrogen-doped carbon (CN) materials. By changing metal precursors or polymers, we demonstrate the successful synthesis of different metal single atoms dispersed on CN materials (SA-M/CN, M = Fe, Co, Ni, Mn, FeCo, FeNi, etc.). Interestingly, the obtained SA-Fe/CN exhibits much higher catalytic activity for hydroxylation of benzene to phenol than Fe nanoparticles/CN (45% vs 5% benzene conversion). First-principle calculations further reveal that the high reactivity originates from the easier formation of activated oxygen species at the single Fe site. Our methodology provides a convenient route to prepare a variety of metal single-atom materials representing a new class of catalysts.
Co-reporter:Shaolong Zhang;Aijuan Han;Yanliang Zhai;Jian Zhang;Weng-Chon Cheong;Yadong Li
Chemical Communications 2017 vol. 53(Issue 68) pp:9490-9493
Publication Date(Web):2017/08/22
DOI:10.1039/C7CC04926A
A facile strategy to prepare sintering- and leaching-resistant core–shell nanocatalysts is reported. ZIF-derived porous carbon supported Pd nanoparticles are coated with a mesoporous silica shell, preventing Pd nanoparticles from sintering at high temperature and leaching in a catalytic process. This nanocatalyst exhibits excellent catalytic activity and recyclability for the oxidation of benzyl alcohol.
Co-reporter:Jiawei Wan;Wenxing Chen;Chen Chen;Qing Peng;Yadong Li
Chemical Communications 2017 vol. 53(Issue 90) pp:12177-12180
Publication Date(Web):2017/11/09
DOI:10.1039/C7CC07115A
We report a pyrolysis reduction method to prepare highly uniform dispersed CoNix nanoparticles embedded in nitrogen–carbon frameworks. With an appropriate value of Ni/Co, the obtained CoNi0.37–CN catalyst exhibited excellent properties and stability in electrocatalytic oxygen evolution, which are superior to those of the commercial IrO2.
Co-reporter:Yuanjun Chen;Shufang Ji;Dr. Yanggang Wang;Dr. Juncai Dong;Dr. Wenxing Chen;Zhi Li;Rongan Shen;Dr. Lirong Zheng; Zhongbin Zhuang; Dr. Dingsheng Wang; Dr. Yadong Li
Angewandte Chemie 2017 Volume 129(Issue 24) pp:7107-7107
Publication Date(Web):2017/06/06
DOI:10.1002/ange.201703992
Isolierte Eisenatome die durch Pyrolyse einer verkapselten Vorstufe erzeugt wurden, katalysieren die Sauerstoffreduktion (ORR) in hoch reaktiver und stabiler Weise. In ihrer Zuschrift auf S. 7041 ff. zeigen D. Wang, Y. Li und Mitarbeiter experimentell und durch Rechnungen, dass das Vorliegen der isolierten Fe-Atome und die Einführung von Stickstoff entscheidend für die ORR-Aktivität sind.
Co-reporter:Yuanjun Chen;Shufang Ji;Dr. Yanggang Wang;Dr. Juncai Dong;Dr. Wenxing Chen;Zhi Li;Rongan Shen;Dr. Lirong Zheng; Zhongbin Zhuang; Dr. Dingsheng Wang; Dr. Yadong Li
Angewandte Chemie 2017 Volume 129(Issue 24) pp:7041-7045
Publication Date(Web):2017/06/06
DOI:10.1002/ange.201702473
AbstractThe development of low-cost, efficient, and stable electrocatalysts for the oxygen reduction reaction (ORR) is desirable but remains a great challenge. Herein, we made a highly reactive and stable isolated single-atom Fe/N-doped porous carbon (ISA Fe/CN) catalyst with Fe loading up to 2.16 wt %. The catalyst showed excellent ORR performance with a half-wave potential (E1/2) of 0.900 V, which outperformed commercial Pt/C and most non-precious-metal catalysts reported to date. Besides exceptionally high kinetic current density (Jk) of 37.83 mV cm−2 at 0.85 V, it also had a good methanol tolerance and outstanding stability. Experiments demonstrated that maintaining the Fe as isolated atoms and incorporating nitrogen was essential to deliver the high performance. First principle calculations further attributed the high reactivity to the high efficiency of the single Fe atoms in transporting electrons to the adsorbed OH species.
Co-reporter:Dr. Wenxing Chen;Jiajing Pei;Dr. Chun-Ting He;Dr. Jiawei Wan;Hanlin Ren;Dr. Youqi Zhu;Dr. Yu Wang;Dr. Juncai Dong;Shubo Tian;Weng-Chon Cheong;Siqi Lu;Dr. Lirong Zheng;Dr. Xusheng Zheng; Wensheng Yan; Zhongbin Zhuang; Chen Chen; Qing Peng; Dingsheng Wang; Yadong Li
Angewandte Chemie 2017 Volume 129(Issue 50) pp:16302-16306
Publication Date(Web):2017/12/11
DOI:10.1002/ange.201710599
AbstractThe highly efficient electrochemical hydrogen evolution reaction (HER) provides a promising pathway to resolve energy and environment problems. An electrocatalyst was designed with single Mo atoms (Mo-SAs) supported on N-doped carbon having outstanding HER performance. The structure of the catalyst was probed by aberration-corrected scanning transmission electron microscopy (AC-STEM) and X-ray absorption fine structure (XAFS) spectroscopy, indicating the formation of Mo-SAs anchored with one nitrogen atom and two carbon atoms (Mo1N1C2). Importantly, the Mo1N1C2 catalyst displayed much more excellent activity compared with Mo2C and MoN, and better stability than commercial Pt/C. Density functional theory (DFT) calculation revealed that the unique structure of Mo1N1C2 moiety played a crucial effect to improve the HER performance. This work opens up new opportunities for the preparation and application of highly active and stable Mo-based HER catalysts.
Co-reporter:Dr. Junjie Mao;Dr. Wenxing Chen;Dr. Wenming Sun;Dr. Zheng Chen;Jiajing Pei;Dr. Dongsheng He;Dr. Chunlin Lv; Dingsheng Wang; Yadong Li
Angewandte Chemie 2017 Volume 129(Issue 39) pp:12133-12137
Publication Date(Web):2017/09/18
DOI:10.1002/ange.201706645
AbstractTuning the selectivity of metal catalysts is of paramount importance yet a great challenge. A new strategy to effectively control the selectivity of metal catalysts, by tuning the lattice strain, is reported. A certain amount of Co atoms is introduced into Ru catalysts to compress the Ru lattice, as confirmed by aberration-corrected high-resolution transmission electron microscopy (HRTEM) and X-ray absorption fine structure (XAFS) measurements. We discover that the lattice strain of Ru catalysts can greatly affect their selectivity, and Ru with 3 % lattice compression exhibits extremely high catalytic selectivity for hydrogenation of 4-nitrostyrene to 4-aminostyrene compared to pristine Ru (99 % vs. 66 %). Theoretical studies confirm that the optimized lateral compressive strain facilitates hydrogenation of the nitro group but impedes the hydrogenation of the vinyl group. This study provides a new guideline for designing metal catalysts with high selectivity.
Co-reporter:Dr. Junjie Mao;Dr. Wenxing Chen;Dr. Wenming Sun;Dr. Zheng Chen;Jiajing Pei;Dr. Dongsheng He;Dr. Chunlin Lv; Dingsheng Wang; Yadong Li
Angewandte Chemie International Edition 2017 Volume 56(Issue 39) pp:11971-11975
Publication Date(Web):2017/09/18
DOI:10.1002/anie.201706645
AbstractTuning the selectivity of metal catalysts is of paramount importance yet a great challenge. A new strategy to effectively control the selectivity of metal catalysts, by tuning the lattice strain, is reported. A certain amount of Co atoms is introduced into Ru catalysts to compress the Ru lattice, as confirmed by aberration-corrected high-resolution transmission electron microscopy (HRTEM) and X-ray absorption fine structure (XAFS) measurements. We discover that the lattice strain of Ru catalysts can greatly affect their selectivity, and Ru with 3 % lattice compression exhibits extremely high catalytic selectivity for hydrogenation of 4-nitrostyrene to 4-aminostyrene compared to pristine Ru (99 % vs. 66 %). Theoretical studies confirm that the optimized lateral compressive strain facilitates hydrogenation of the nitro group but impedes the hydrogenation of the vinyl group. This study provides a new guideline for designing metal catalysts with high selectivity.
Co-reporter:Yuanjun Chen;Shufang Ji;Dr. Yanggang Wang;Dr. Juncai Dong;Dr. Wenxing Chen;Zhi Li;Rongan Shen;Dr. Lirong Zheng; Zhongbin Zhuang; Dr. Dingsheng Wang; Dr. Yadong Li
Angewandte Chemie International Edition 2017 Volume 56(Issue 24) pp:7003-7003
Publication Date(Web):2017/06/06
DOI:10.1002/anie.201703992
Isolated single-atom iron catalysts with excellent oxygen reduction reaction (ORR) reactivity and outstanding stability are prepared by a cage-encapsulated-precursor pyrolysis strategy. In their Communication on page 6937 ff., D. Wang, Y. Li, and co-workers show experimentally and theoretically that it is essential for the high ORR performance to maintain the iron centers as isolated atoms as well as to incorporate nitrogen.
Co-reporter:Yuanjun Chen;Shufang Ji;Dr. Yanggang Wang;Dr. Juncai Dong;Dr. Wenxing Chen;Zhi Li;Rongan Shen;Dr. Lirong Zheng; Zhongbin Zhuang; Dr. Dingsheng Wang; Dr. Yadong Li
Angewandte Chemie International Edition 2017 Volume 56(Issue 24) pp:6937-6941
Publication Date(Web):2017/06/06
DOI:10.1002/anie.201702473
AbstractThe development of low-cost, efficient, and stable electrocatalysts for the oxygen reduction reaction (ORR) is desirable but remains a great challenge. Herein, we made a highly reactive and stable isolated single-atom Fe/N-doped porous carbon (ISA Fe/CN) catalyst with Fe loading up to 2.16 wt %. The catalyst showed excellent ORR performance with a half-wave potential (E1/2) of 0.900 V, which outperformed commercial Pt/C and most non-precious-metal catalysts reported to date. Besides exceptionally high kinetic current density (Jk) of 37.83 mV cm−2 at 0.85 V, it also had a good methanol tolerance and outstanding stability. Experiments demonstrated that maintaining the Fe as isolated atoms and incorporating nitrogen was essential to deliver the high performance. First principle calculations further attributed the high reactivity to the high efficiency of the single Fe atoms in transporting electrons to the adsorbed OH species.
Co-reporter:Yuxi Liu;Xiangwen Liu;Quanchen Feng;Dongsheng He;Libo Zhang;Chao Lian;Rongan Shen;Guofeng Zhao;Yongjun Ji;Gang Zhou;Yadong Li
Advanced Materials 2016 Volume 28( Issue 23) pp:4747-4754
Publication Date(Web):
DOI:10.1002/adma.201600603
Co-reporter:Hongpan Rong;Junjie Mao;Pingyu Xin;Dongsheng He;Yuanjun Chen;Zhiqiang Niu;Yuen Wu;Yadong Li
Advanced Materials 2016 Volume 28( Issue 13) pp:2540-2546
Publication Date(Web):
DOI:10.1002/adma.201504831
Co-reporter:Jiajing Pei, Junjie Mao, Xin Liang, Chen Chen, Qing Peng, Dingsheng Wang and Yadong Li  
Chemical Communications 2016 vol. 52(Issue 19) pp:3793-3796
Publication Date(Web):03 Feb 2016
DOI:10.1039/C6CC00552G
Herein, we achieved successful synthesis of uniform Ir–Cu nanoframes with highly open structures by a facile one-pot strategy. The key to obtain alloy nanoframes was the careful control over the reduction and galvanic replacement reactions between different metals. The as-prepared Ir–Cu was proved to be an effective template for constructing trimetallic nanoframes. Furthermore, these highly open nanostructures exhibited excellent electrocatalytic performance toward oxygen evolution reaction in alkaline media.
Co-reporter:Junjie Mao, Yuanjun Chen, Jiajing Pei, Dingsheng Wang and Yadong Li  
Chemical Communications 2016 vol. 52(Issue 35) pp:5985-5988
Publication Date(Web):01 Apr 2016
DOI:10.1039/C6CC02264B
Herein, we exploit two typical crystal growth modes, namely, “stacking” and “carving” routes, to synthesize Pt-based bimetallic nanomaterials with defect-rich surface structures, which exhibit enhanced electrocatalytic properties toward both methanol oxidation reaction (MOR) and oxygen reduction reaction (ORR) compared with commercial Pt/C.
Co-reporter:Junjie Mao, Zheng Chen, Yuanjun Chen, Dingsheng Wang and Yadong Li  
CrystEngComm 2016 vol. 18(Issue 21) pp:3764-3767
Publication Date(Web):28 Apr 2016
DOI:10.1039/C6CE00588H
In this work, Pt–Cu nanocrystals (NCs) with octahedral and multi-octahedral structures were facilely prepared by a wet chemistry method. Furthermore, we have evaluated the catalytic activity of these Pt–Cu NCs, and the results indicated that the composition and morphology strongly influence the catalytic performance in the p-chloronitrobenzene hydrogenation and methanol electro-oxidation reactions, respectively.
Co-reporter:Junjie Mao, Jiajing Pei, Qing Peng, Dingsheng Wang and Yadong Li  
CrystEngComm 2016 vol. 18(Issue 22) pp:4023-4026
Publication Date(Web):11 Jan 2016
DOI:10.1039/C5CE02478A
Pt-based branched nanocrystals (NCs) have attracted much attention because of their unique properties. In this work, we employed a facile and efficient route to synthesize highly branched Pt–Pd–M (M = Co, Ni) trimetallic NCs via a one-pot strategy in an octadecylamine (ODA) system. The formation process and influencing factors of the reaction were discussed based on the experimental observations. Further electrochemical measurements indicated that the branched NCs showed enhanced catalytic activities.
Co-reporter:Dr. Xiaofei Yu;Dr. Lanlan Li;Yanqiu Su;Dr. Wei Jia;Lili Dong;Dr. Dingsheng Wang;Dr. Jianling Zhao;Dr. Yadong Li
Chemistry - A European Journal 2016 Volume 22( Issue 14) pp:4960-4965
Publication Date(Web):
DOI:10.1002/chem.201600079

Abstract

Platinum–copper nanoframes were produced from copper nanoparticles by a one-pot synthesis method. The growth mechanism was thoroughly studied by experiment and theoretical calculations. Owing to the unique structure, Pt-Cu nanoframes exhibited significantly enhanced catalytic activity toward the electro-oxidation of methanol compared to commercial Pt black.

Co-reporter:Zheng Chen;Shuo Wang;Dr. Chao Lian;Dr. Yuxi Liu;Dr. Dingsheng Wang;Dr. Chen Chen;Dr. Qing Peng;Dr. Yadong Li
Chemistry – An Asian Journal 2016 Volume 11( Issue 3) pp:351-355
Publication Date(Web):
DOI:10.1002/asia.201500531

Abstract

It is highly challenging but desirable to develop efficient heterogeneous catalysts for C−Cl bond activation in coupling reactions. Here, we succeeded in synthesizing bimetallic Pd-Au nanoparticles through a convenient one-pot wet chemical route. The composition and alloyed structure of the as-prepared nanoparticles were fully characterized. We have evaluated the catalytic activity of these Pd-Au alloy catalysts in Buchwald–Hartwig reactions of aryl chlorides. The excellent catalytic activity of the as-obtained Pd-Au nanoparticles indicates that exploiting the catalytic power of nano-alloy catalysts could enable effective C−Cl bond activation suitable for cross-coupling reactions.

Co-reporter:Haohong Duan, Dingsheng Wang and Yadong Li  
Chemical Society Reviews 2015 vol. 44(Issue 16) pp:5778-5792
Publication Date(Web):23 Jan 2015
DOI:10.1039/C4CS00363B
The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods.
Co-reporter:Wei Jia, Yuxi Liu, Pengfei Hu, Rong Yu, Yu Wang, Lei Ma, Dingsheng Wang and Yadong Li  
Chemical Communications 2015 vol. 51(Issue 42) pp:8817-8820
Publication Date(Web):21 Apr 2015
DOI:10.1039/C5CC02480C
Ultrathin copper oxide (CuO) nanorods with diameters of ∼3.6 nm were obtained in one step using oleylamine (OAm) as both the solvent and the surface controller. The oriented attachment is responsible for the formation of the ultrathin CuO nanorods. Furthermore, this ultrathin nanostructure catalyst exhibited excellent activity and high styrene oxide yields in styrene epoxidation.
Co-reporter:Yixuan Zhou, Yongpeng Lei, Dingsheng Wang, Chen Chen, Qing Peng and Yadong Li  
Chemical Communications 2015 vol. 51(Issue 68) pp:13305-13308
Publication Date(Web):15 Jul 2015
DOI:10.1039/C5CC05156H
Herein, we achieved successful synthesis of 2D Cu2S nanosheets (NS) with a thickness of 1.2 nm by a novel strategy. The key to obtain ultra-thin Cu2S NS was the use of a unique sulfur precursor which not only supplied sulfur in a controlled manner, but also directed the formation of a 2D structure. The as-prepared Cu2S NS were proved to be effective cocatalysts for photocatalytic hydrogen production. The H2 production rate of Cu2S NS/TiO2 reached 1430.4 μmol g−1 h−1, which was 4.9 times higher than that of TiO2.
Co-reporter:Junjie Mao, Tai Cao, Yuanjun Chen, Yuen Wu, Chen Chen, Qing Peng, Dingsheng Wang and Yadong Li  
Chemical Communications 2015 vol. 51(Issue 84) pp:15406-15409
Publication Date(Web):27 Aug 2015
DOI:10.1039/C5CC06740E
In this work, we present a facile etching–reduction–selective epitaxial growth synergistic strategy to synthesize trimetallic nanocrystals. The methodology demonstrated here provides some general guidelines for the design and fabrication of multimetallic heteronanostructures, which would open up new opportunities for practical fuel cell applications or other chemical reactions.
Co-reporter:Tai Cao;Jiatao Zhang;Chuanbao Cao;Yadong Li
Chemistry - A European Journal 2015 Volume 21( Issue 40) pp:14022-14029
Publication Date(Web):
DOI:10.1002/chem.201502040

Abstract

In recent years, various non-precious metal electrocatalysts for the oxygen reduction reaction (ORR) have been extensively investigated. The development of an efficient and simple method to synthesize non-precious metal catalysts with ORR activity superior to that of Pt is extremely significant for large-scale applications of fuel cells. Here, we develop a facile, low-cost, and large-scale synthesis method for uniform nitrogen-doped (N-doped) bamboo-like CNTs (NBCNT) with Co nanoparticles encapsulated at the tips by annealing a mixture of cobalt acetate and melamine. The uniform NBCNT shows better ORR catalytic activity and higher stability in alkaline solutions as compared with commercial Pt/C and comparable catalytic activity to Pt/C in acidic media. NBCNTs exhibit outstanding ORR catalytic activity due to high defect density, uniform bamboo-like structure, and the synergistic effect between the Co nanoparticles and protective graphitic layers. This facile method to synthesize catalysts, which is amenable to the large-scale commercialization of fuel cells, will open a new avenue for the development of low-cost and high-performance ORR catalysts to replace Pt-based catalysts for applications in energy conversion.

Co-reporter:Yuen Wu, Dingsheng Wang and Yadong Li  
Chemical Society Reviews 2014 vol. 43(Issue 7) pp:2112-2124
Publication Date(Web):24 Oct 2013
DOI:10.1039/C3CS60221D
The ultimate goal of nanoscale science and technology is to manipulate single atoms, assemble atoms in a controllable way and design nanostructured materials with the desired physical and chemical properties (e.g. catalytic properties). In order to achieve this goal, the nucleation and growth mechanism of nanocrystals (NCs) as well as the relationship between the macroscopic properties and microscopic structures of nanocrystals should be fully understood. In this tutorial review, we firstly summarize the latest research developments and experimental methods to exploit the nucleation and growth process of nanocrystals, then discuss the essence of nanocrystal catalysis, and finally present our personal perspectives on the opportunities and challenges of this promising field.
Co-reporter:Junjie Mao, Yuxi Liu, Zheng Chen, Dingsheng Wang and Yadong Li  
Chemical Communications 2014 vol. 50(Issue 35) pp:4588-4591
Publication Date(Web):17 Mar 2014
DOI:10.1039/C4CC01051E
Monodisperse Pd–Cu bimetallic nanocrystals (NCs) with tunable compositions (Pd0.2Cu0.8, Pd0.3Cu0.7, Pd0.5Cu0.5, Pd0.7Cu0.3, Pd0.8Cu0.2) and controlled sizes (5.2 nm, 6.8 nm, 8.1 nm, 16.4 nm, 19.9 nm) were easily obtained in an octadecylamine (ODA) synthetic system, which exhibited tunable catalytic properties for styrene epoxidation and ethanol electro-oxidation.
Co-reporter:Yixuan Zhou, Dingsheng Wang and Yadong Li  
Chemical Communications 2014 vol. 50(Issue 46) pp:6141-6144
Publication Date(Web):16 Apr 2014
DOI:10.1039/C4CC02081B
We developed a facile one-pot synthetic strategy to prepare highly branched metal nanocrystals including monometallic Pd and bimetallic Au@Pd nanodendrites, and demonstrated their superior catalytic properties.
Co-reporter:Junjie Mao, Dingsheng Wang, Guofeng Zhao, Wei Jia and Yadong Li  
CrystEngComm 2013 vol. 15(Issue 24) pp:4806-4810
Publication Date(Web):15 Apr 2013
DOI:10.1039/C3CE40458G
Bimetallic nanocrystals can be successfully synthesized via coreduction of mixed metal ions in a liquid–solid–solution synthetic system. In this effective system, non-noble metal ions that cannot be reduced by ethanol can be reduced to zero valence metals in the presence of noble metal ions.
Co-reporter:Junjie Mao, Yuanjun Chen, Jiajing Pei, Dingsheng Wang and Yadong Li
Chemical Communications 2016 - vol. 52(Issue 35) pp:NaN5988-5988
Publication Date(Web):2016/04/01
DOI:10.1039/C6CC02264B
Herein, we exploit two typical crystal growth modes, namely, “stacking” and “carving” routes, to synthesize Pt-based bimetallic nanomaterials with defect-rich surface structures, which exhibit enhanced electrocatalytic properties toward both methanol oxidation reaction (MOR) and oxygen reduction reaction (ORR) compared with commercial Pt/C.
Co-reporter:Wei Jia, Yuxi Liu, Pengfei Hu, Rong Yu, Yu Wang, Lei Ma, Dingsheng Wang and Yadong Li
Chemical Communications 2015 - vol. 51(Issue 42) pp:NaN8820-8820
Publication Date(Web):2015/04/21
DOI:10.1039/C5CC02480C
Ultrathin copper oxide (CuO) nanorods with diameters of ∼3.6 nm were obtained in one step using oleylamine (OAm) as both the solvent and the surface controller. The oriented attachment is responsible for the formation of the ultrathin CuO nanorods. Furthermore, this ultrathin nanostructure catalyst exhibited excellent activity and high styrene oxide yields in styrene epoxidation.
Co-reporter:Jiajing Pei, Junjie Mao, Xin Liang, Chen Chen, Qing Peng, Dingsheng Wang and Yadong Li
Chemical Communications 2016 - vol. 52(Issue 19) pp:NaN3796-3796
Publication Date(Web):2016/02/03
DOI:10.1039/C6CC00552G
Herein, we achieved successful synthesis of uniform Ir–Cu nanoframes with highly open structures by a facile one-pot strategy. The key to obtain alloy nanoframes was the careful control over the reduction and galvanic replacement reactions between different metals. The as-prepared Ir–Cu was proved to be an effective template for constructing trimetallic nanoframes. Furthermore, these highly open nanostructures exhibited excellent electrocatalytic performance toward oxygen evolution reaction in alkaline media.
Co-reporter:Yixuan Zhou, Yongpeng Lei, Dingsheng Wang, Chen Chen, Qing Peng and Yadong Li
Chemical Communications 2015 - vol. 51(Issue 68) pp:NaN13308-13308
Publication Date(Web):2015/07/15
DOI:10.1039/C5CC05156H
Herein, we achieved successful synthesis of 2D Cu2S nanosheets (NS) with a thickness of 1.2 nm by a novel strategy. The key to obtain ultra-thin Cu2S NS was the use of a unique sulfur precursor which not only supplied sulfur in a controlled manner, but also directed the formation of a 2D structure. The as-prepared Cu2S NS were proved to be effective cocatalysts for photocatalytic hydrogen production. The H2 production rate of Cu2S NS/TiO2 reached 1430.4 μmol g−1 h−1, which was 4.9 times higher than that of TiO2.
Co-reporter:Junjie Mao, Tai Cao, Yuanjun Chen, Yuen Wu, Chen Chen, Qing Peng, Dingsheng Wang and Yadong Li
Chemical Communications 2015 - vol. 51(Issue 84) pp:NaN15409-15409
Publication Date(Web):2015/08/27
DOI:10.1039/C5CC06740E
In this work, we present a facile etching–reduction–selective epitaxial growth synergistic strategy to synthesize trimetallic nanocrystals. The methodology demonstrated here provides some general guidelines for the design and fabrication of multimetallic heteronanostructures, which would open up new opportunities for practical fuel cell applications or other chemical reactions.
Co-reporter:Junjie Mao, Yuxi Liu, Zheng Chen, Dingsheng Wang and Yadong Li
Chemical Communications 2014 - vol. 50(Issue 35) pp:NaN4591-4591
Publication Date(Web):2014/03/17
DOI:10.1039/C4CC01051E
Monodisperse Pd–Cu bimetallic nanocrystals (NCs) with tunable compositions (Pd0.2Cu0.8, Pd0.3Cu0.7, Pd0.5Cu0.5, Pd0.7Cu0.3, Pd0.8Cu0.2) and controlled sizes (5.2 nm, 6.8 nm, 8.1 nm, 16.4 nm, 19.9 nm) were easily obtained in an octadecylamine (ODA) synthetic system, which exhibited tunable catalytic properties for styrene epoxidation and ethanol electro-oxidation.
Co-reporter:Yixuan Zhou, Dingsheng Wang and Yadong Li
Chemical Communications 2014 - vol. 50(Issue 46) pp:NaN6144-6144
Publication Date(Web):2014/04/16
DOI:10.1039/C4CC02081B
We developed a facile one-pot synthetic strategy to prepare highly branched metal nanocrystals including monometallic Pd and bimetallic Au@Pd nanodendrites, and demonstrated their superior catalytic properties.
Co-reporter:Haohong Duan, Dingsheng Wang and Yadong Li
Chemical Society Reviews 2015 - vol. 44(Issue 16) pp:NaN5792-5792
Publication Date(Web):2015/01/23
DOI:10.1039/C4CS00363B
The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods.
Co-reporter:Yuen Wu, Dingsheng Wang and Yadong Li
Chemical Society Reviews 2014 - vol. 43(Issue 7) pp:NaN2124-2124
Publication Date(Web):2013/10/24
DOI:10.1039/C3CS60221D
The ultimate goal of nanoscale science and technology is to manipulate single atoms, assemble atoms in a controllable way and design nanostructured materials with the desired physical and chemical properties (e.g. catalytic properties). In order to achieve this goal, the nucleation and growth mechanism of nanocrystals (NCs) as well as the relationship between the macroscopic properties and microscopic structures of nanocrystals should be fully understood. In this tutorial review, we firstly summarize the latest research developments and experimental methods to exploit the nucleation and growth process of nanocrystals, then discuss the essence of nanocrystal catalysis, and finally present our personal perspectives on the opportunities and challenges of this promising field.
Benzene, 1-[(1,1-dimethylethoxy)methyl]-4-nitro-
Formamide, N-(4-acetylphenyl)-
Benzenamine, 4-[(phenylmethoxy)methyl]-
Benzenemethanamine, N,N-dimethyl-2-nitro-
Benzenamine, N,N-dibutyl-4-fluoro-
Benzenemethanamine, 4-amino-N-cyclohexyl-N-methyl-
Naphthalene, 1-[(3-nitrophenyl)methoxy]-
Benzenemethanamine, 4-amino-N,N-dipropyl-
Benzenemethanamine, 4-nitro-N,N-dipropyl-
Gallium, compd. with nickel (1:3)