Mengmeng Zhang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Mengmeng Zhang has a total of 101 co-authors. Here are the top co-authors by number of shared publications:
- Zhijia Zhang
School of Material Science and Engineering, State Key Laboratory of Separation Membrane and Membrane Processes, Tiangong University, Tianjin, China
6 shared publications Yong Jiang
School of Materials Science and Engineering, State Key Laboratory of Separation Membrane and Membrane Processes, Tiangong University, Tianjin, 300387, China; School of Electronic and Information Engineering, Institute of Quantum Materials and Devices, Tiangong University, Tianjin, 300387, China
5 shared publicationsYida Deng
State Key Laboratory of Marine Resource Utilization in South China Sea, School of Materials Science and Engineering, Hainan University, Haikou 570228, China
4 shared publications- Cheng Zhong
Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education), and Tianjin Key Laboratory of Composite and Functional Materials, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China
3 shared publications Dayong Cai
Key laboratory of Metastable Materials Science & Technology, Yanshan University, Qinhuangdao 066004, China
3 shared publicationsHui Xue
School of Materials Science and Engineering, Tiangong University, Tianjin, China
3 shared publications
Latest Publications
- 9 May 2026
- Published by Springer Nature in Catalysis Letters
- Vol. 156 (6) , 156
Doping S Tailors the Electronic Structure of CuBiOx Catalyst for Selective CO2 Electroreduction to CO
- 9 May 2026
- Published by Springer Nature in Catalysis Letters
- Vol. 156 (6) , 156
Doping S Tailors the Electronic Structure of CuBiOx Catalyst for Selective CO2 Electroreduction to CO
- 22 March 2026
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 716, 140356
Steering carbon dioxide electroreduction toward formic acid by Sn-induced Cu0 stabilization and optimized *OCHO intermediate adsorption
- 22 March 2026
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 716, 140356
Steering carbon dioxide electroreduction toward formic acid by Sn-induced Cu0 stabilization and optimized *OCHO intermediate adsorption
- Open Access
- 17 April 2024
- Published by OAE Publishing Inc. in Microstructures
- Vol. 4 (2)
Research progress of amorphous catalysts in the field of electrocatalysis
Amorphous materials feature unique structures and physicochemical properties, resulting in their synthesis and applications becoming a dynamic and fascinating new research direction. The high specific surface area, abundant active sites, and good electron transport properties endow amorphous materials with excellent electrocatalytic properties, thus appealing to increasing attention. Based on this, the summary of the current research status of amorphous catalysts in the field of electrocatalysis is urgent and important. In this review, the research progress of amorphous catalysts in electrocatalysis is systematically introduced, focusing on the classification, synthesis methods, modification strategies, characterizations, and electrocatalytic application (including hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, carbon dioxide reduction reaction, and nitrogen reduction reaction). Finally, this review proposes the prospects and challenges for the future development of high-active and high-selectivity amorphous electrocatalysts.
- 17 April 2024
- Published by OAE Publishing Inc. in Microstructures
- Vol. 4 (2)
Open AccessResearch progress of amorphous catalysts in the field of electrocatalysis
Amorphous materials feature unique structures and physicochemical properties, resulting in their synthesis and applications becoming a dynamic and fascinating new research direction. The high specific surface area, abundant active sites, and good electron transport properties endow amorphous materials with excellent electrocatalytic properties, thus appealing to increasing attention. Based on this, the summary of the current research status of amorphous catalysts in the field of electrocatalysis is urgent and important. In this review, the research progress of amorphous catalysts in electrocatalysis is systematically introduced, focusing on the classification, synthesis methods, modification strategies, characterizations, and electrocatalytic application (including hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, carbon dioxide reduction reaction, and nitrogen reduction reaction). Finally, this review proposes the prospects and challenges for the future development of high-active and high-selectivity amorphous electrocatalysts.
- 17 November 2023
- Published by Elsevier in Materials Research Bulletin
- Vol. 171, 112621
Multiphase interface engineering based on porous manganous oxide toward broad-band microwave absorption
- 17 November 2023
- Published by Elsevier in Materials Research Bulletin
- Vol. 171, 112621
Multiphase interface engineering based on porous manganous oxide toward broad-band microwave absorption
- Top Cited Papers
- 23 September 2023
- Published by Wiley in Rare Metals
- Vol. 42 (11) , 3607-3613
Optimized valence state of Co and Ni in high‐entropy alloy for high active‐stable OER
摘要: 高熵合金表现出良好潜在的电催化水分解性能,但其受到制备过程中高能耗的限制。此外,复杂的原子分布使高熵合金的电子结构调控仍然具有很大的挑战性。本文采用高能球磨结合去合金化方法制备了纳米多孔NiCuMnCoFe高熵合金。Fe的引入显著提高了Ni 3+ 和Co 3+ 的比例。大量高价态Ni和Co原子有利于在析氧反应过程中形成关键的活性中间体,并赋予纳米多孔NiCuMnCoFe高熵合金283 mV的低过电位和81.09 mV·dec ‐1 的优异Tafel斜率(10 mA·cm ‐2 )。同时,纳米多孔NiCuMnCoFe高熵合金表现出优异的耐久性,其活性优于大多数其他报道的高熵合金类催化剂。优化的d带中心决定了纳米多孔NiCuMnCoFe高熵合金中Fe、Co和Ni位点中间体的吸附和解吸之间的平衡,并确定了析氧反应的决速步是O 2 形成步骤。这项工作为调控高熵合金的元素价态并实现高效电催化水分解铺平道路。
- 23 September 2023
- Published by Wiley in Rare Metals
- Vol. 42 (11) , 3607-3613
Top Cited PapersOptimized valence state of Co and Ni in high‐entropy alloy for high active‐stable OER
摘要: 高熵合金表现出良好潜在的电催化水分解性能,但其受到制备过程中高能耗的限制。此外,复杂的原子分布使高熵合金的电子结构调控仍然具有很大的挑战性。本文采用高能球磨结合去合金化方法制备了纳米多孔NiCuMnCoFe高熵合金。Fe的引入显著提高了Ni 3+ 和Co 3+ 的比例。大量高价态Ni和Co原子有利于在析氧反应过程中形成关键的活性中间体,并赋予纳米多孔NiCuMnCoFe高熵合金283 mV的低过电位和81.09 mV·dec ‐1 的优异Tafel斜率(10 mA·cm ‐2 )。同时,纳米多孔NiCuMnCoFe高熵合金表现出优异的耐久性,其活性优于大多数其他报道的高熵合金类催化剂。优化的d带中心决定了纳米多孔NiCuMnCoFe高熵合金中Fe、Co和Ni位点中间体的吸附和解吸之间的平衡,并确定了析氧反应的决速步是O 2 形成步骤。这项工作为调控高熵合金的元素价态并实现高效电催化水分解铺平道路。
- 2 August 2023
- Published by Elsevier in Journal of Materials Science & Technology
- Vol. 171, 16-23
Regulating the intrinsic electronic structure of carbon nanofibers with high-spin state Ni for sodium storage with high-power density
- 2 August 2023
- Published by Elsevier in Journal of Materials Science & Technology
- Vol. 171, 16-23
Regulating the intrinsic electronic structure of carbon nanofibers with high-spin state Ni for sodium storage with high-power density
- Open Access
- 1 June 2022
- Published by IOP Publishing in Journal of Physics: Conference Series
- Vol. 2202 (1) , 012032
Effect of concrete under continuous load on demoulding time during construction
Based on the current construction progress of each floor of the building, under the action of continuous construction load, the concrete strength at this time is only about 80% of that at the same age without load. It is suggested that when the test block maintained under the same conditions reaches 85% of the design strength, the whole structure is not easy to crack, which is not safe.
- 1 June 2022
- Published by IOP Publishing in Journal of Physics: Conference Series
- Vol. 2202 (1) , 012032
Open AccessEffect of concrete under continuous load on demoulding time during construction
Based on the current construction progress of each floor of the building, under the action of continuous construction load, the concrete strength at this time is only about 80% of that at the same age without load. It is suggested that when the test block maintained under the same conditions reaches 85% of the design strength, the whole structure is not easy to crack, which is not safe.