研究者詳細

顔写真

ワン　メン
Wang Meng
Wang Meng
所属
高等研究機構材料科学高等研究所　デバイス・システムグループ
職名
特任助教（研究）
学位

  • Ｐｈ．Ｄ．（National University of Singapore）

  • Ｍ．Ｓ．（Shanghai Normal University）

e-Rad 研究者番号
81027259

経歴 2

  • 2025年5月 ～ 継続中
    Specially Appointed Assistant Professor

  • 2024年2月 ～ 2025年4月
    Research Fellow - National University of Singapore　Chemistry

学歴 1

  • National University of Singapore　Chemistry

    2020年8月 ～ 2024年6月

研究キーワード 4

  • 界面触媒

  • Li-O2 Battery

  • Photocathode Interface Design

  • Metal-Air Battery

研究分野 2

  • ナノテク・材料 / エネルギー化学 /

  • ナノテク・材料 / ナノ材料科学 /

受賞 4

  1. IJMS Best Poster Award

    2023年11月　9th National Meeting for Surface Science and Applications

  2. PhD Conference Award

    2023年5月　National University of Singapore

  3. Best Research Presentation Award

    2022年12月　National University of Singapore-Tianjin University

  4. The Electrochemical Society Best Poster Award

    2021年6月　the 2nd Singapore ECS International Symposium on Energy Materials

論文 21

  1. Edge‐Dislocated WO3 Photocathode Toward Efficient Photo‐Assisted Li‐O2 Batteries 査読有り

    Meng Wang, Zhangliu Tian, Guanxing Li, Yukun Xiao, Ganwen Chen, Siyuan Li, Ruiqi Su, Baihua Cui, Chonglai Jiang, Zejun Sun, Haotian Yang, Yu Long, Hui Zhang, Yu Han, Hexing Li, Wei Chen

    Advanced Materials　2025年7月21日

    出版者・発行元： Wiley

    DOI： 10.1002/adma.202501716 　

    ISSN：0935-9648

    eISSN：1521-4095

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    Abstract The operation of rechargeable Li‐O2 batteries critically depends on the highly reversible formation and decomposition of Li2O2 at the cathode. However, the intrinsic insulating nature of Li2O2 fundamentally restricts reaction kinetics, posing a core challenge to practical applications. Here, it is demonstrate that the insulating properties of Li2O2 can be effectively improved by photoexcitation, attributed to the generation of photo‐induced charge carriers. It is inspired to develop photo‐assisted Li‐O2 batteries featuring Z‐type photocathode@Li2O2 heterojunction, which serves as a charge modulation channel to regulate carrier dynamics through photocathode modifications. By employing edge‐dislocated WO3 as the photocathode, sustained growth of Li2O2 films is observed with a thickness >18 µm, which is 2–3 orders of magnitude higher than typically reported values. Benefiting from the enhanced exciton dissociation of Li2O2 and improved oxidative capability of photocathode, the battery delivers an ultra‐high discharge capacity of 31 800 mAh g−1 under a current density of 100 mA g−1 and a light‐induced temperature of ≈60 °C. In addition, a low polarization overpotential of 0.04 V is achieved with high reversibility over 1 000 h. The grasp of photoexcited Li2O2 within Li‐O2 batteries can drive solutions beyond state‐of‐the‐art metal‐air batteries.

  2. Photocathode Design in Photo‐Assisted Li‐O2 Batteries: Status and Perspectives 査読有り

    Meng Wang, Ganwen Chen, Zhangliu Tian, Ruiqi Su, Chonglai Jiang, Zejun Sun, Yuan Liu, Wei Chen

    SmartMat　6　(2)　2025年4月8日

    出版者・発行元： Wiley

    DOI： 10.1002/smm2.70004 　

    ISSN：2766-8525

    eISSN：2688-819X

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    ABSTRACT Li‐O2 batteries with an ultrahigh theoretical energy density of up to 3500 W·h/kg have drawn extensive attention as future energy storage technologies. However, large discharge/charge overpotentials (> 1 V) and unsatisfactory cycling performance are the main obstacles for practical applications. Recently, integrating photocatalysis into Li‐O2 batteries has emerged as a promising method to mitigate overpotentials, but the rational design of photocathodes with excellent photoelectrochemical activity and stability remains challenging. This review focuses on recent research progress on the reaction mechanisms in photo‐assisted Li‐O2 batteries and the development of photocathodes. We present several strategies for tailoring catalytic materials from the perspectives of material selection and its catalytic performance optimization, aiming to provide a fundamental understanding and insights into the design of efficient photocathodes. The key challenges in constructing high‐performance photocathodes and potential strategies were also discussed, offering insights for the development and application of efficient photocathodes in photo‐assisted Li‐O2 batteries.

  3. Selective and Energy Efficient Electrocatalytic CO2‐to‐Ethanol Conversion through Anion Modulation 査読有り

    Yumin Da, Jie Chen, Lei Fan, Rui Jiang, Yukun Xiao, Meng Wang, Ganwen Chen, Zhangliu Tian, Hanqian Zhang, Hongqiang Jin, Xiang Chen, Chenrui Ji, Shibo Xi, Yanwei Lum, Lei Wang, Tong Zhu, Jia Zhang, Wei Chen

    Angewandte Chemie International Edition　64　(35)　2025年7月9日

    出版者・発行元： Wiley

    DOI： 10.1002/anie.202506867 　

    ISSN：1433-7851

    eISSN：1521-3773

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    Abstract Ethanol, with its high market value and stable global demand, stands out as an attractive product of electrocatalytic CO2 reduction. However, achieving high ethanol selectivity and energy efficiency at industrial current densities remains challenging. In this study, we employed a blended anion modulation strategy to enhance the selectivity and energy efficiency of CO2‐to‐ethanol conversion. The Cu2(OH)3F pre‐catalyst achieved Faradaic efficiencies of 50% and 93% for ethanol and C2+, respectively, at 700 mA cm−2 in a blended electrolyte consisting of 2 M KOH and 1 M KCl. Comprehensive electrochemical tests, combined with in situ characterizations and theoretical analysis, revealed that chloride and hydroxide increased *CO coverage for efficient C─C coupling. Moreover, hydroxide stabilizes the *CHCOH intermediate through hydrogen bonding with the adsorbed hydroxide on the catalyst surface, while Cl synergistically enhances its reactivity by promoting water dissociation toward the ethanol pathway.

  4. Deciphering and Enhancing Rate‐Determining Step of Sodium Deposition towards Ultralow‐Temperature Sodium Metal Batteries 査読有り

    Yuxiang Niu, Jinlin Yang, Fanbin Meng, Zejun Sun, Chonglai Jiang, Yuan Liu, Hongfei Xu, Meng Wang, Haotian Yang, Yupeng Zhu, Gang Wu, Wei Chen

    Angewandte Chemie International Edition　64　(8)　2025年1月28日

    出版者・発行元： Wiley

    DOI： 10.1002/anie.202416720 　

    ISSN：1433-7851

    eISSN：1521-3773

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    Abstract Achieving high ionic conductivity and stable performance at low temperatures remains a significant challenge in sodium‐metal batteries (SMBs). In this study, we propose a novel electrolyte design strategy that elucidates the solvation structure‐function relationship within mixed solvent systems. A mixture of diglyme and 1,3‐dioxolane was developed to optimize the solvation structure towards superior low‐temperature electrolyte. Molecular dynamics simulations and Raman spectra results reveal the solvent‐separated ion pairs and contact ion pairs dominated solvation structure in the designed electrolyte, displaying a superior ionic conductivity of 1.78×10−3 S cm−1 at −40 °C. Besides, comprehensive kinetic analysis shows Na+ transportation in the electrolyte shows a greater impact on sodium plating than Na+ transport through the solid electrolyte interphase or charge transfer. As a result, the electrolyte enables stable operation for over 12,000 hours in NaNa cells at −40 °C. In NaNa2/3Ni1/4Cu1/12Mn2/3O2 full cells, it maintains a high capacity retention of 92.4 % over 600 cycles with an initial specific capacity of 89.4 mAh g−1 at −40 °C, and achieves 81.7 % capacity retention after 50 cycles with an initial specific capacity of 75.3 mAh g−1 at −78 °C. These results pave the way for the development of high‐performance SMBs capable of operating under ultralow temperatures.

  5. n‐ZrS3/p‐ZrOS Photoanodes with NiOOH/FeOOH Oxygen Evolution Catalysts for Photoelectrochemical Water Oxidation 査読有り

    Zhangliu Tian, Meng Wang, Ganwen Chen, Jie Chen, Yumin Da, Hanqian Zhang, Rui Jiang, Yukun Xiao, Baihua Cui, Chonglai Jiang, Yishui Ding, Jinlin Yang, Zejun Sun, Cheng Han, Wei Chen

    Angewandte Chemie　137　(2)　2024年11月7日

    出版者・発行元： Wiley

    DOI： 10.1002/ange.202414209 　

    ISSN：0044-8249

    eISSN：1521-3757

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    Abstract Photoelectrochemical water splitting offers a promising approach for carbon neutrality, but its commercial prospects are still hampered by a lack of efficient and stable photoelectrodes with earth‐abundant materials. Here, we report a strategy to construct an efficient photoanode with a coaxial nanobelt structure, comprising a buried‐ZrS3/ZrOS n−p junction, for photoelectrochemical water splitting. The p‐type ZrOS layer, formed on the surface of the n‐type ZrS3 nanobelt through a pulsed‐ozone‐treatment method, acts as a hole collection layer for hole extraction and a protective layer to shield the photoanode from photocorrosion. The resulting ZrS3/ZrOS photoanode exhibits light harvesting with good photo‐to‐current efficiencies across the whole visible region to over 650 nm. By further employing NiOOH/FeOOH as the oxygen evolution reaction cocatalyst, the ZrS3/ZrOS/NiOOH/FeOOH photoanode yields a photocurrent density of ~9.3 mA cm−2 at 1.23 V versus the reversible hydrogen electrode with an applied bias photon‐to‐current efficiency of ~3.2 % under simulated sunlight irradiation in an alkaline solution (pH=13.6). The conformal ZrOS layer enables ZrS3/ZrOS/NiOOH/FeOOH photoanode operation over 1000 hours in an alkaline solution without obvious performance degradation. This study, offering a promising approach to fabricate efficient and durable photoelectrodes with earth‐abundant materials, advances the frontiers of photoelectrochemical water splitting.

  6. Boosting photoelectrocatalytic hydrogen evolution of Bi@OV-BiOBr/Cu3P high-low heterojunction with dual-channel charge transfer 査読有り

    Xibao Li, Tao Han, Yingtang Zhou, Meng Wang, Zhangliu Tian, Fang Deng, Yidan Luo, Yu Xie, Juntong Huang, Lu Han, Zhi Chen, Zhijun Feng, Wei Chen

    Applied Catalysis B: Environment and Energy　350　123913-123913　2024年8月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.apcatb.2024.123913 　

    ISSN：0926-3373

  7. Realization of Two‐Dimensional Intrinsic Polar Metal in a Buckled Honeycomb Binary Lattice 査読有り

    Yihe Wang, Dong Li, Sisheng Duan, Shuo Sun, Yishui Ding, Fabio Bussolotti, Mingyue Sun, Mingxi Chen, Meng Wang, Lan Chen, Kehui Wu, Kuan Eng Johnson Goh, Andrew T. S. Wee, Miao Zhou, Baojie Feng, Chenqiang Hua, Yu Li Huang, Wei Chen

    Advanced Materials　2024年7月18日

    出版者・発行元： Wiley

    DOI： 10.1002/adma.202404341 　

    ISSN：0935-9648

    eISSN：1521-4095

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    Abstract Structural topology and symmetry of a two‐dimensional (2D) network play pivotal roles in defining its electrical properties and functionalities. Here, a binary buckled honeycomb lattice with C3v symmetry, which naturally hosts topological Dirac fermions and out‐of‐plane polarity, is proposed. It is successfully achieved in a group IV‐V compound, namely monolayer SiP epitaxially grown on Ag(111) surface. Combining first‐principles calculations with angle‐resolved photoemission spectroscopy, the degeneration of the Dirac nodal lines to points due to the broken horizonal mirror symmetry is elucidated. More interesting, the SiP monolayer manifests metallic nature, which is mutually exclusive with polarity in conventional materials. It is further found that the out‐of‐plane polarity is strongly suppressed by the metallic substrate. This study not only represents a breakthrough of realizing intrinsic polarity in 2D metallic material via ingenious design but also provides a comprehensive understanding of the intricate interplay of many exotic low‐dimensional quantum phenomena.

  8. Metal-enzyme nanogel biochemical composite: An efficient platform for one-pot dynamic kinetic resolution of amines 査読有り

    Meng Wang, Jie Sheng, Leyi Gu, Xiaoxu Wang, Weihua Cheng, Peiyi Ji, Shenfang Jiang, Yuanzhe Huang, Zonglin Li, Chenhao Zhang, Hui Li

    Journal of Cleaner Production　458　142441-142441　2024年6月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.jclepro.2024.142441 　

    ISSN：0959-6526

  9. Homogenizing Interfacial Temperature Distribution for High Performance Solid-State Lithium Metal Batteries 査読有り

    Chonglai Jiang, Haotian Lu, Jinlin Yang, Zejun Sun, Yukun Xiao, Yuxiang Niu, Hongfei Xu, Yuan Liu, Meng Wang, Haotian Yang, Baihua Cui, Yu Long, Ganwen Chen, Yi Shan, Quan-Hong Yang, Wei Chen

    ACS Energy Letters　9　(6)　2527-2535　2024年5月6日

    出版者・発行元： American Chemical Society (ACS)

    DOI： 10.1021/acsenergylett.4c00964 　

    ISSN：2380-8195

    eISSN：2380-8195

  10. Revealing the effect of metal-support interactions at the Ni/In2O3(111) interface on the selective CO2 hydrogenation 査読有り

    Yishui Ding, Jie Chen, Xu Lian, Zhangliu Tian, Xiangrui Geng, Yihe Wang, Yuan Liu, Wei Wang, Meng Wang, Yukun Xiao, Tengyu Jin, Mingyue Sun, Zhenni Yang, Kelvin H.L. Zhang, Jian-Qiang Zhong, Wei Chen

    Applied Catalysis B: Environmental　343　123508-123508　2024年4月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.apcatb.2023.123508 　

    ISSN：0926-3373

  11. Intermediate State of Dense Ru Assembly Captured by High-Temperature Shock for Durable Ampere-Level Hydrogen Production 査読有り

    Baihua Cui, He Zhu, Meng Wang, Jianrong Zeng, Jinfeng Zhang, Zhangliu Tian, Chonglai Jiang, Zejun Sun, Haotian Yang, Yuan Liu, Jia Ding, Ziyi Luo, Yanan Chen, Wei Chen, Wenbin Hu

    ACS Materials Letters　6　(4)　1532-1541　2024年3月18日

    出版者・発行元： American Chemical Society (ACS)

    DOI： 10.1021/acsmaterialslett.4c00124 　

    ISSN：2639-4979

    eISSN：2639-4979

  12. Enabling an Inorganic-Rich Interface via Cationic Surfactant for High-Performance Lithium Metal Batteries 査読有り

    Zejun Sun, Jinlin Yang, Hongfei Xu, Chonglai Jiang, Yuxiang Niu, Xu Lian, Yuan Liu, Ruiqi Su, Dayu Liu, Yu Long, Meng Wang, Jingyu Mao, Haotian Yang, Baihua Cui, Yukun Xiao, Ganwen Chen, Qi Zhang, Zhenxiang Xing, Jisheng Pan, Gang Wu, Wei Chen

    Nano-Micro Letters　16　(1)　2024年3月4日

    出版者・発行元： Springer Science and Business Media LLC

    DOI： 10.1007/s40820-024-01364-x 　

    ISSN：2311-6706

    eISSN：2150-5551

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    Abstract An anion-rich electric double layer (EDL) region is favorable for fabricating an inorganic-rich solid–electrolyte interphase (SEI) towards stable lithium metal anode in ester electrolyte. Herein, cetyltrimethylammonium bromide (CTAB), a cationic surfactant, is adopted to draw more anions into EDL by ionic interactions that shield the repelling force on anions during lithium plating. In situ electrochemical surface-enhanced Raman spectroscopy results combined with molecular dynamics simulations validate the enrichment of NO3−/FSI− anions in the EDL region due to the positively charged CTA+. In-depth analysis of SEI structure by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry results confirmed the formation of the inorganic-rich SEI, which helps improve the kinetics of Li+ transfer, lower the charge transfer activation energy, and homogenize Li deposition. As a result, the Li||Li symmetric cell in the designed electrolyte displays a prolongated cycling time from 500 to 1300 h compared to that in the blank electrolyte at 0.5 mA cm−2 with a capacity of 1 mAh cm−2. Moreover, Li||LiFePO4 and Li||LiCoO2 with a high cathode mass loading of > 10 mg cm−2 can be stably cycled over 180 cycles.

  13. Catalytic Solid‐State Sulfur Conversion Confined in Micropores toward Superhigh Coulombic Efficiency Lithium‐Sulfur Batteries 査読有り

    Haotian Yang, Li Wang, Chuannan Geng, Yufei Zhao, Qiang Li, Xin Jiang, Zhangliu Tian, Meng Wang, Chonglai Jiang, Zejun Sun, Baihua Cui, Yan‐Bing He, Wei Chen, Wei Lv, Quan‐Hong Yang

    Advanced Energy Materials　14　(21)　2024年3月3日

    出版者・発行元： Wiley

    DOI： 10.1002/aenm.202400249 　

    ISSN：1614-6832

    eISSN：1614-6840

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    Abstract Achieving the solid–solid conversion of sulfur is a fundamental solution to eliminating the shuttling of soluble polysulfides and improving the cycling stability of lithium‐sulfur batteries. However, the sluggish solid reaction kinetics seriously challenge the battery performance. In this work, a micropore‐confined catalysis strategy to achieve the smooth solid–solid conversion of sulfur is proposed. It is realized by storing sulfur in a microporous carbon host with narrow pore size and uniformly distributed single‐atom Co catalytic sites. The microporous structure avoids the contact of electrolyte solvents with the inner sulfur, preventing the formation and dissolution of polysulfides and efficiently suppressing sulfur loss during cycling. The introduced single‐atom Co catalytic sites promote the charge transfer to accelerate the solid–solid conversion of sulfur. When coupled with a liquid carbonate electrolyte, the battery exhibits a remarkably high Coulombic efficiency (CE) of ≈99.88% and a minimal capacity decay rate of ≈0.016% per cycle for 1000 cycles at 0.5 C. Even when coupled with the solid‐state electrolyte, the battery still delivers a significantly high capacity of 1100 mAh g−1 and a remarkably high CE of ≈99.83% over 200 cycles. This work reveals a promising solution for developing practical stable Li─S batteries.

  14. Multi‐Shell Copper Catalysts for Selective Electroreduction of CO2to Multicarbon Chemicals 査読有り

    Yukun Xiao, Meng Wang, Haozhou Yang, Haoran Qiu, Haotian Lu, Yumin Da, Ganwen Chen, Tianyuan Jiang, Weiwei Fu, Bihao Hu, Junmei Chen, Lei Chen, Yishui Ding, Baihua Cui, Chonglai Jiang, Zejun Sun, Yu Long, Haotian Yang, Zhangliu Tian, Lei Wang, Wei Chen

    Advanced Energy Materials　14　(1)　2023年11月13日

    出版者・発行元： Wiley

    DOI： 10.1002/aenm.202302556 　

    ISSN：1614-6832

    eISSN：1614-6840

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    Abstract Electrocatalytic CO2reduction (CO2R) coupled with renewable electricity has been considered as a promising route for the sustainability transition of energy and chemical industries. However, the unsatisfactory yield of desired products, particularly multicarbon (C2+) products, has hindered the implementation of this technology. This work describes a strategy to enhance the yield of C2+product formation in CO2R by utilizing spatial confinement effects. The finite element simulation results suggest that increasing the number of shells in the catalyst wil lead to a high local concentration of *CO and promotes the formation of C2+products. Inspired by this, Cu nanoparticles are synthesized with desired hollow multi‐shell structures. The CO2reduction results confirm that as the number of shells increase, the hollow multi‐shell copper catalysts exhibit improved selectivity toward C2+products. Specifically, the Cu catalyst with 4.4‐shell achieved a high selectivity of over 80% toward C2+at a current density of 900 mA cm−2. Evidence from in situ attenuated total reflection surface‐enhanced infrared absorption spectroscopy unveils that the multi‐shell Cu catalyst exhibits an enhanced *COatopcoverage and the stronger interaction with *COatopcompared to commercial Cu, confirming the simulation results. Overall, the work promises an effective approach for boosting CO2R selectivity toward value‐added chemicals.

  15. Rational Design of Benzo‐Crown Ether Electrolyte Additives for High‐Performance Li‐O2 Batteries 査読有り

    Qi Zhang, Yuke Li, Eng Tuan Poh, Zhenxiang Xing, Mingsheng Zhang, Meng Wang, Zejun Sun, Jisheng Pan, Sai Vikrama Chaitanya Vummaleti, Jia Zhang, Wei Chen

    Advanced Energy Materials　13　(37)　2023年8月17日

    出版者・発行元： Wiley

    DOI： 10.1002/aenm.202301748 　

    ISSN：1614-6832

    eISSN：1614-6840

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    Abstract Despite theoretical predictions of exceptional gravimetric energy densities in Li‐O2 batteries (LOBs), the current research forefront faces challenges, including high charge overpotential, cathode clogging, parasitic reactions, and Li anode corrosion. Herein, benzo‐crown ethers (BCEs) with varying cavity sizes are used as electrolyte additives to exploit their strong binding toward Li+ and promote the solution growth of Li2O2 with reduced particle size. Notably, the cell with benzo‐18‐crown‐6 ether (B18C6) enables the largest discharge capacity of 14948 mAh g−1. Upon charging, these additives accelerate Li2O2 oxidation through the strong binding with Li+ and the extended electrolyte/Li2O2 interface, resulting in improved reversibility, reduced charge overpotential, and prolonged cycle life. Besides, these additives also stabilize the Li anode by regulating Li+ migration and electron exchange, reducing dendritic growth and anode corrosion. This work presents insights into the rational design of BCEs as additives for high‐performance LOBs.

  16. Selective photoelectrochemical oxidation of glucose to glucaric acid by single atom Pt decorated defective TiO2 査読有り

    Zhangliu Tian, Yumin Da, Meng Wang, Xinyu Dou, Xinhang Cui, Jie Chen, Rui Jiang, Shibo Xi, Baihua Cui, Yani Luo, Haotian Yang, Yu Long, Yukun Xiao, Wei Chen

    Nature Communications　14　(1)　2023年1月10日

    出版者・発行元： Springer Science and Business Media LLC

    DOI： 10.1038/s41467-023-35875-9 　

    eISSN：2041-1723

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    Abstract Photoelectrochemical reaction is emerging as a powerful approach for biomass conversion. However, it has been rarely explored for glucose conversion into value-added chemicals. Here we develop a photoelectrochemical approach for selective oxidation of glucose to high value-added glucaric acid by using single-atom Pt anchored on defective TiO2 nanorod arrays as photoanode. The defective structure induced by the oxygen vacancies can modulate the charge carrier dynamics and band structure, simultaneously. With optimized oxygen vacancies, the defective TiO2 photoanode shows greatly improved charge separation and significantly enhanced selectivity and yield of C6 products. By decorating single-atom Pt on the defective TiO2 photoanode, selective oxidation of glucose to glucaric acid can be achieved. In this work, defective TiO2 with single-atom Pt achieves a photocurrent density of 1.91 mA cm−2 for glucose oxidation at 0.6 V versus reversible hydrogen electrode, leading to an 84.3 % yield of glucaric acid under simulated sunlight irradiation.

  17. Facet-controlled bifunctional WO3photocathodes for high-performance photo-assisted Li–O2batteries 査読有り

    Meng Wang, Jie Chen, Zhangliu Tian, Wenrui Dai, Baihua Cui, Xinhang Cui, Dong Wang, Yukun Xiao, Xu Lian, Chonglai Jiang, Haotian Yang, Yihe Wang, Zejun Sun, Yishui Ding, Yi-Yang Sun, Jia Zhang, Wei Chen

    Energy & Environmental Science　16　(2)　523-534　2023年

    出版者・発行元： Royal Society of Chemistry (RSC)

    DOI： 10.1039/d2ee03724f 　

    ISSN：1754-5692

    eISSN：1754-5706

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    Facet-engineered monoclinic WO3was investigated to explore the effects on the photo-assisted LOB kinetics and discharge mechanism. This work can pave the way for rational photocathode design in metal–O2batteries.

  18. Monodispersed Ruthenium Nanoparticles on Nitrogen-Doped Reduced Graphene Oxide for an Efficient Lithium–Oxygen Battery 査読有り

    Wenrui Dai, Yuan Liu, Meng Wang, Ming Lin, Xu Lian, Yani Luo, Jinlin Yang, Wei Chen

    ACS Applied Materials & Interfaces　13　(17)　19915-19926　2021年4月21日

    出版者・発行元： American Chemical Society (ACS)

    DOI： 10.1021/acsami.0c23125 　

    ISSN：1944-8244

    eISSN：1944-8252

  19. Combining Pd nanoparticles on MOFs with cross-linked enzyme aggregates of lipase as powerful chemoenzymatic platform for one-pot dynamic kinetic resolution of amines 査読有り

    Meng Wang, Xiaoxu Wang, Bo Feng, Yuanhua Li, Xinchen Han, Zijie Lan, Huajun Gu, Huamin Sun, Meng Shi, Hexing Li, Hui Li

    Journal of Catalysis　378　153-163　2019年10月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.jcat.2019.08.033 　

    ISSN：0021-9517

  20. Controlled Assembly of Hierarchical Metal Catalysts with Enhanced Performances 査読有り

    Meng Wang, Bo Feng, Hui Li, Hexing Li

    Chem　5　(4)　805-837　2019年4月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.chempr.2019.01.003 　

    ISSN：2451-9294

  21. Dynamic kinetic resolution of amines by using palladium nanoparticles confined inside the cages of amine-modified MIL-101 and lipase 査読有り

    Sen Xu, Meng Wang, Bo Feng, Xinchen Han, Zijie Lan, Huajun Gu, Hexing Li, Hui Li

    Journal of Catalysis　363　9-17　2018年7月

    出版者・発行元： Elsevier BV

    DOI： 10.1016/j.jcat.2018.04.006 　

    ISSN：0021-9517

︎全件表示 ︎最初の5件までを表示

産業財産権 5

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    産業財産権の種類: 特許権

  3. 単原子Pt修飾欠陥TiO₂を用いた、高付加価値グルカール酸へのグルコース選択的光電気化学酸化の高効率フォトアノード

    産業財産権の種類: 特許権

  4. 高性能光補助Li–O₂電池のための二機能性光触媒としての結晶面制御WO₃光陰極

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  5. 架橋酵素触媒およびその応用

    産業財産権の種類: 特許権

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