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Ruisheng Zhao

Researcher at Xi'an Jiaotong University

Publications -  6
Citations -  378

Ruisheng Zhao is an academic researcher from Xi'an Jiaotong University. The author has contributed to research in topics: Chemistry & Catalysis. The author has an hindex of 2, co-authored 2 publications receiving 265 citations.

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Controllable Design of MoS2 Nanosheets Anchored on Nitrogen-Doped Graphene: Toward Fast Sodium Storage by Tunable Pseudocapacitance

TL;DR: A simple solvothermal method to synthesize a series of MoS2 nanosheets@nitrogen-doped graphene composites is developed, demonstrating the significance in surface-controlled pseudocapacitance contribution at the high rate and offering some meaningful preparation and investigation experiences for designing electrode materials for commercial sodium-ion batteries with favorable performance.
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Progressively Exposing Active Facets of 2D Nanosheets toward Enhanced Pseudocapacitive Response and High-Rate Sodium Storage.

TL;DR: Three kinds of tin (IV) sulfide nanosheets are controllably designed with progressively exposed active facets, leading to beneficial influences on the Na+ storage kinetics, resulting in gradient improvements of pseudocapacitive response and rate performance.
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Theoretical study on the stabilities, electronic structures, and reaction and formation mechanisms of fullerenes and endohedral metallofullerenes

TL;DR: In this article , the authors highlight the advanced theoretical contributions to the structures, reaction mechanisms, and formation mechanisms of fullerenes, including endohedral fullerene (EFs), including their derivatives.
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Water-Tolerant Boron-Substituted MCM-41 for Oxidative Dehydrogenation of Propane

TL;DR: In this article , a series of mesoporous B-MCM-41 (BM-x, B/Si = 0.015-0.147) catalysts for ODHP were prepared by a simple hydrothermal synthesis method.
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Copper-Catalyzed Transamidation of Unactivated Secondary Amides via C-H and C-N Bond Simultaneous Activations.

TL;DR: In this paper , the authors demonstrate that α-C-H and C-N bonds of unactivated secondary amides can be activated simultaneously by the copper catalyst to synthesize α-ketoamides or αketoesters in one step.