Yu Zhang

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Name: 张瑜; Yu Zhang
Organization: Beihang University
Department: 1 State Key Laboratory of Rare Earth Resource Utilization
Title: Researcher/Professor

TOPICS

Co-reporter:Xu Zou;Yipu Liu;Guo-Dong Li;Yuanyuan Wu;Da-Peng Liu;Wang Li;Hai-Wen Li;Dejun Wang;Xiaoxin Zou
Advanced Materials 2017 Volume 29(Issue 22) pp:
Publication Date(Web):2017/06/01
DOI:10.1002/adma.201700404
Developing nonprecious oxygen evolution electrocatalysts that can work well at large current densities is of primary importance in a viable water-splitting technology. Herein, a facile ultrafast (5 s) synthetic approach is reported that produces a novel, efficient, non-noble metal oxygen-evolution nano-electrocatalyst that is composed of amorphous Ni–Fe bimetallic hydroxide film-coated, nickel foam (NF)-supported, Ni3S2 nanosheet arrays. The composite nanomaterial (denoted as Ni-Fe-OH@Ni3S2/NF) shows highly efficient electrocatalytic activity toward oxygen evolution reaction (OER) at large current densities, even in the order of 1000 mA cm−2. Ni-Fe-OH@Ni3S2/NF also gives an excellent catalytic stability toward OER both in 1 m KOH solution and in 30 wt% KOH solution. Further experimental results indicate that the effective integration of high catalytic reactivity, high structural stability, and high electronic conductivity into a single material system makes Ni-Fe-OH@Ni3S2/NF a remarkable catalytic ability for OER at large current densities.
Co-reporter:Xiaoxian Zhao;Ranbo Yu;Hongjie Tang;Dan Mao;Jian Qi;Bao Wang;Huijun Zhao;Wenping Hu;Dan Wang
Advanced Materials 2017 Volume 29(Issue 34) pp:
Publication Date(Web):2017/09/01
DOI:10.1002/adma.201700550
The multishelled (Co2/3Mn1/3)(Co5/6Mn1/6)2O4 hollow microspheres with controllable shell numbers up to septuple shells are synthesized using developed sequential templating method. Exhilaratingly, the septuple-shelled complex metal oxide hollow microsphere is synthesized for the first time by doping Mn into Co3O4, leading to the change of crystalline rate of precursor. Used as electrode materials for alkaline rechargeable battery, it shows a remarkable reversible capacity (236.39 mAh g−1 at a current density of 1 A g−1 by three-electrode system and 106.85 mAh g−1 at 0.5 A g−1 in alkaline battery) and excellent cycling performance due to its unique structure.
Co-reporter:Heng-Guo Wang;Wang Li;Da-Peng Liu;Xi-Lan Feng;Jin Wang;Xiao-Yang Yang;Xin-bo Zhang;Yujie Zhu
Advanced Materials 2017 Volume 29(Issue 45) pp:
Publication Date(Web):2017/12/01
DOI:10.1002/adma.201703012
AbstractSodium-ion batteries (SIBs) are considered as promising alternatives to lithium-ion batteries (LIBs) for large-scale electrical-energy-storage applications due to the wide availability and the low cost of Na resources. Along with the avenues of research on flexible LIBs, flexible SIBs are now being actively developed as one of the most promising power sources for the emerging field of flexible and wearable electronic devices. Here, the recent progress on flexible electrodes based on metal substrates, carbonaceous substrates (i.e., graphene, carbon cloth, and carbon nanofibers), and other materials, as well as their applications in flexible SIBs, are summarized. Also, some future research directions for constructing flexible SIBs are proposed, with the aim of providing inspiration to the further development of advanced flexible SIBs.
Co-reporter:Wang Li, Xilan Feng, Zheng Zhang, Dapeng Liu, Yu Zhang
Materials Research Bulletin 2017 Volume 96, Part 1(Volume 96, Part 1) pp:
Publication Date(Web):1 December 2017
DOI:10.1016/j.materresbull.2016.12.001
•A series of CeO2/Co3O4 catalysts were synthesized via a convenient and facile one-pot method.•The catalytic performance on CO oxidation could be optimized by tuning the molar ratios of Ce and Co elements.•This strategy facilitates mass production, and the only use of water and ethanol solvents show a green environmental advantage.Mixed metal oxides with hybrid structures often show synergistic effects and thus much better catalytic properties than their single components. We present here the synthesis of Ce/Co mixed oxalates via a facile co-precipitation method, and the following calcination process resulted in the final CeO2/Co3O4 hybrid microstructures. Then the systematical characterizations were conducted to study their structure evolution and composition-dependent properties on catalytic CO oxidation. The results show that the hybrids of CeO2/Co3O4 were composed of 5 nm sized CeO2 and 20 nm sized Co3O4. While increasing the feeding amount of Ce, the morphologies of the as-obtained CeO2/Co3O4 hybrids changed from the flower-like microstructures to the hot dog-like ones, and finally to the sheet-like ones. After catalytic tests, it was found that the CeO2/Co3O4 hybrids show different catalytic activities by varying the molar ratios of Ce/Co (pure Co for Co-oxalate, Ce/Co = 1/19 for Ce1/Co19-oxalate, Ce/Co = 1/9 for Ce1/Co9-oxalate, Ce/Co = 3/7 for Ce3/Co7-oxalate, Ce/Co = 5/5 for Ce5/Co5-oxalate, pure Ce for Ce-oxalate). Among these samples, Ce/Co = 1:19, which has a higer pore volume performed the optimal catalytic property compared to the others.Download high-res image (195KB)Download full-size image
Co-reporter:Fan Wang, Wang Li, Xilan Feng, Dapeng Liu and Yu Zhang  
Chemical Science 2016 vol. 7(Issue 3) pp:1867-1873
Publication Date(Web):25 Nov 2015
DOI:10.1039/C5SC04069H
In this paper, we report an efficient strategy for the synthesis of Cu/Co double-doped CeO2 nanospheres (CuxCo1−x–CeO2–Pt, 0 ≤ x ≤ 1), which were fabricated via a simple water–glycol system. The following in situ surface decoration of Pt nanoparticles make these nanospheres highly active for the catalytic reduction of nitrophenol and CO oxidation. Detailed tests show that their catalytic performance strongly depends on the doping components and ion concentration of Cu and Co ions. The best samples of Cu0.50Co0.50–CeO2–Pt and Cu0.34Co0.66–CeO2–Pt demonstrate an excellent turnover frequency (TOF) of more than 450 h−1 after five cycles and retains about 99% conversion by using NH3BH3 as a reductant to reduce nitrophenol. Moreover, Cu0.50Co0.50–CeO2–Pt possesses a much lower light-off and T100 (the temperature for 100% CO oxidation) temperature compared with the other catalysts.
Co-reporter:Wang Li 李旺;Xilan Feng 冯锡岚;Dapeng Liu 刘大鹏 张瑜
Science China Materials 2016 Volume 59( Issue 3) pp:191-199
Publication Date(Web):2016 March
DOI:10.1007/s40843-016-5038-1
A facile in situ redox strategy has been developed to fabricate surfactant-free M-Fe2O3 (M = Pt, Pd, Au) hybrid nanospheres. In this process, noble metal salts were directly reduced by the pre-prepared Fe3O4 components in an alkaline aqueous solution without using organic reductants and surfactants. During the redox reaction, Fe3O4 was oxidized into Fe2O3, and the reduzates of noble metal nanoparticles were deposited on the surface of the Fe2O3 nanospheres. Then the characterizations were discussed in detail to study the formation of M-Fe2O3 hybrids. At last, catalytic CO oxidation was selected as a model reaction to evaluate the catalytic performance of these samples. It demonstrates that Pt-Fe2O3 nanospheres can catalyze 100 % conversion of CO into CO2 at 90°C, indicating superior activity relative to Pd-Fe2O3 and Au-Fe2O3.本工作利用原位氧化还原策略, 成功制备出无表面活性剂修饰的M-Fe2O3(M=Pt, Pd, Au)杂化纳米球. 在反应过程中, 以事先制备好的Fe3O4纳米球作为载体和还原剂, 在碱性条件下直接还原高价态的贵金属盐前躯体. 反应后, Fe3O4被氧化成Fe2O3, 而贵金属纳米粒子作为还原产物则牢牢的沉积在氧化产物Fe2O3表面形成M-Fe2O3杂化纳米球. 通过表征系统研究了所得产物的形貌、结构和催化性质. 并以CO催化氧化为模型反应对产物进行评估, 结果表明, 样品Pt-Fe2O3在90°C即可将CO 100%催化转化为CO2, 相比Pd-Fe2O3和Au-Fe2O3具有更高的催化活性.
Co-reporter:Xiaoxin Zou and Yu Zhang  
Chemical Society Reviews 2015 vol. 44(Issue 15) pp:5148-5180
Publication Date(Web):17 Apr 2015
DOI:10.1039/C4CS00448E
Sustainable hydrogen production is an essential prerequisite of a future hydrogen economy. Water electrolysis driven by renewable resource-derived electricity and direct solar-to-hydrogen conversion based on photochemical and photoelectrochemical water splitting are promising pathways for sustainable hydrogen production. All these techniques require, among many things, highly active noble metal-free hydrogen evolution catalysts to make the water splitting process more energy-efficient and economical. In this review, we highlight the recent research efforts toward the synthesis of noble metal-free electrocatalysts, especially at the nanoscale, and their catalytic properties for the hydrogen evolution reaction (HER). We review several important kinds of heterogeneous non-precious metal electrocatalysts, including metal sulfides, metal selenides, metal carbides, metal nitrides, metal phosphides, and heteroatom-doped nanocarbons. In the discussion, emphasis is given to the synthetic methods of these HER electrocatalysts, the strategies of performance improvement, and the structure/composition-catalytic activity relationship. We also summarize some important examples showing that non-Pt HER electrocatalysts could serve as efficient cocatalysts for promoting direct solar-to-hydrogen conversion in both photochemical and photoelectrochemical water splitting systems, when combined with suitable semiconductor photocatalysts.
Co-reporter:Jun Wang;Wang Li;Yuren Wen;Lin Gu
Advanced Energy Materials 2015 Volume 5( Issue 10) pp:
Publication Date(Web):
DOI:10.1002/aenm.201401879
Co-reporter:Shanlong Li, Nengli Wang, Yonghai Yue, Guangsheng Wang, Zhao Zu and Yu Zhang  
Chemical Science 2015 vol. 6(Issue 4) pp:2495-2500
Publication Date(Web):10 Feb 2015
DOI:10.1039/C5SC00129C
Copper doped ceria porous nanostructures with a tunable BET surface area were prepared using an efficient and general metal–organic-framework-driven, self-template route. The XRD, SEM and TEM results indicate that Cu2+ was successfully substituted into the CeO2 lattice and well dispersed in the CeO2:Cu2+ nanocrystals. The CeO2:Cu2+ nanocrystals exhibit a superior bifunctional catalytic performance for CO oxidation and selective catalytic reduction of NO. Interestingly, CO oxidation reactivity over the CeO2:Cu2+ nanocrystals was found to be dependent on the Cu2+ dopants and BET surface area. By tuning the content of Cu2+ and BET surface area through choosing different organic ligands, the 100% conversion temperature of CO over CeO2:Cu2+ nanocrystals obtained from thermolysis of CeCu–BPDC nanocrystals can be decreased to 110 °C. The porous nanomaterials show a high CO conversion rate without any loss in activity even after five cycles. Furthermore, the activity of the catalysts for NO reduction increased with the increase of BET surface, which is in accordance with the results of CO oxidation.
Co-reporter:Dapeng Liu, Wang Li, Xilan Feng and Yu Zhang  
Chemical Science 2015 vol. 6(Issue 12) pp:7015-7019
Publication Date(Web):07 Sep 2015
DOI:10.1039/C5SC02774H
A galvanic replacement strategy has been successfully adopted to design AgxAu1−x@CeO2 core@shell nanospheres derived from Ag@CeO2 ones. After etching using HAuCl4, the Ag core was in situ replaced with AgxAu1−x alloy nanoframes, and void spaces were left under the CeO2 shell. Among the as-prepared AgxAu1−x@CeO2 catalysts, Ag0.64Au0.36@CeO2 shows the optimal catalytic performance, whose catalytic efficiency reaches even 2.5 times higher than our previously reported Pt@CeO2 nanospheres in the catalytic reduction of 4-nitrophenol (4-NP) by ammonia borane (AB). Besides, Ag0.64Au0.36@CeO2 also exhibits a much lower 100% conversion temperature of 120 °C for catalytic CO oxidation compared with the other samples.
Co-reporter:Jun Wang;Yang Li
Advanced Functional Materials 2014 Volume 24( Issue 45) pp:7073-7077
Publication Date(Web):
DOI:10.1002/adfm.201401731

Hydrous hydrazine (H2NNH2·H2O) has generally been considered a promising hydrogen storage carrier because of inherent advantages such as its high hydrogen content and easy recharging as a liquid. Unfortunately, the decomposition of hydrous hydrazine to H2 is terribly sluggish and/or not entirely favored—a competing decomposition to ammonia may be preferred. This has been the case using noble-metal catalysts and using non-precious-metal-based catalysts, even at elevated temperatures. To overcome this challenge, non-precious-metal-based Cu@Fe5Ni5 core@shell nanocatalysts are prepared using an in situ seeding-growth approach. Unexpectedly, the catalyst exerts 100% H2 selectivity and excellent activity and stability toward the complete decomposition of hydrous hydrazine, which is due to the synergistic effect of the core@shell structure. These promising results will certainly promote the effective application of hydrous hydrazine as a potential hydrogen storage material.

Co-reporter:De-long Ma, Heng-guo Wang, Yang Li, Dan Xu, Shuang Yuan, Xiao-lei Huang, Xin-bo Zhang, Yu Zhang
Nano Energy 2014 10() pp: 295-304
Publication Date(Web):
DOI:10.1016/j.nanoen.2014.10.004
Co-reporter:Xiao-lei Huang;Ru-zhi Wang;Dan Xu;Zhong-li Wang;Heng-guo Wang;Ji-jing Xu;Zhong Wu;Qing-chao Liu;Xin-bo Zhang
Advanced Functional Materials 2013 Volume 23( Issue 35) pp:
Publication Date(Web):
DOI:10.1002/adfm.201370174
Co-reporter:Xiao-lei Huang;Ru-zhi Wang;Dan Xu;Zhong-li Wang;Heng-guo Wang;Ji-jing Xu;Zhong Wu;Qing-chao Liu;Xin-bo Zhang
Advanced Functional Materials 2013 Volume 23( Issue 35) pp:4345-4353
Publication Date(Web):
DOI:10.1002/adfm.201203777

Abstract

Ultralong cycle life, high energy, and power density rechargeable lithium-ion batteries are crucial to the ever-increasing large-scale electric energy storage for renewable energy and sustainable road transport. However, the commercial graphite anode cannot perform this challenging task due to its low theoretical capacity and poor rate-capability performance. Metal oxides hold much higher capacity but still are plagued by low rate capability and serious capacity degradation. Here, a novel strategy is developed to prepare binder-free and mechanically robust CoO/graphene electrodes, wherein homogenous and full coating of β-Co(OH)2 nanosheets on graphene, through a novel electrostatic induced spread growth method, plays a key role. The combined advantages of large 2D surface and moderate inflexibility of the as-obtained β-Co(OH)2/graphene hybrid enables its easy coating on Cu foil by a simple layer-by-layer stacking process. Devices made with these electrodes exhibit high rate capability over a temperature range from 0 to 55 °C and, most importantly, maintain excellent cycle stability up to 5000 cycles even at a high current density.

Co-reporter:Shanlong Li, Nengli Wang, Yonghai Yue, Guangsheng Wang, Zhao Zu and Yu Zhang
Chemical Science (2010-Present) 2015 - vol. 6(Issue 4) pp:NaN2500-2500
Publication Date(Web):2015/02/10
DOI:10.1039/C5SC00129C
Copper doped ceria porous nanostructures with a tunable BET surface area were prepared using an efficient and general metal–organic-framework-driven, self-template route. The XRD, SEM and TEM results indicate that Cu2+ was successfully substituted into the CeO2 lattice and well dispersed in the CeO2:Cu2+ nanocrystals. The CeO2:Cu2+ nanocrystals exhibit a superior bifunctional catalytic performance for CO oxidation and selective catalytic reduction of NO. Interestingly, CO oxidation reactivity over the CeO2:Cu2+ nanocrystals was found to be dependent on the Cu2+ dopants and BET surface area. By tuning the content of Cu2+ and BET surface area through choosing different organic ligands, the 100% conversion temperature of CO over CeO2:Cu2+ nanocrystals obtained from thermolysis of CeCu–BPDC nanocrystals can be decreased to 110 °C. The porous nanomaterials show a high CO conversion rate without any loss in activity even after five cycles. Furthermore, the activity of the catalysts for NO reduction increased with the increase of BET surface, which is in accordance with the results of CO oxidation.
Co-reporter:Xiaoxin Zou and Yu Zhang
Chemical Society Reviews 2015 - vol. 44(Issue 15) pp:NaN5180-5180
Publication Date(Web):2015/04/17
DOI:10.1039/C4CS00448E
Sustainable hydrogen production is an essential prerequisite of a future hydrogen economy. Water electrolysis driven by renewable resource-derived electricity and direct solar-to-hydrogen conversion based on photochemical and photoelectrochemical water splitting are promising pathways for sustainable hydrogen production. All these techniques require, among many things, highly active noble metal-free hydrogen evolution catalysts to make the water splitting process more energy-efficient and economical. In this review, we highlight the recent research efforts toward the synthesis of noble metal-free electrocatalysts, especially at the nanoscale, and their catalytic properties for the hydrogen evolution reaction (HER). We review several important kinds of heterogeneous non-precious metal electrocatalysts, including metal sulfides, metal selenides, metal carbides, metal nitrides, metal phosphides, and heteroatom-doped nanocarbons. In the discussion, emphasis is given to the synthetic methods of these HER electrocatalysts, the strategies of performance improvement, and the structure/composition-catalytic activity relationship. We also summarize some important examples showing that non-Pt HER electrocatalysts could serve as efficient cocatalysts for promoting direct solar-to-hydrogen conversion in both photochemical and photoelectrochemical water splitting systems, when combined with suitable semiconductor photocatalysts.
Co-reporter:Dapeng Liu, Wang Li, Xilan Feng and Yu Zhang
Chemical Science (2010-Present) 2015 - vol. 6(Issue 12) pp:NaN7019-7019
Publication Date(Web):2015/09/07
DOI:10.1039/C5SC02774H
A galvanic replacement strategy has been successfully adopted to design AgxAu1−x@CeO2 core@shell nanospheres derived from Ag@CeO2 ones. After etching using HAuCl4, the Ag core was in situ replaced with AgxAu1−x alloy nanoframes, and void spaces were left under the CeO2 shell. Among the as-prepared AgxAu1−x@CeO2 catalysts, Ag0.64Au0.36@CeO2 shows the optimal catalytic performance, whose catalytic efficiency reaches even 2.5 times higher than our previously reported Pt@CeO2 nanospheres in the catalytic reduction of 4-nitrophenol (4-NP) by ammonia borane (AB). Besides, Ag0.64Au0.36@CeO2 also exhibits a much lower 100% conversion temperature of 120 °C for catalytic CO oxidation compared with the other samples.
Co-reporter:Fan Wang, Wang Li, Xilan Feng, Dapeng Liu and Yu Zhang
Chemical Science (2010-Present) 2016 - vol. 7(Issue 3) pp:
Publication Date(Web):
DOI:10.1039/C5SC04069H
Nitric acid, cerium(3+)salt (3:1)