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Author

Jiangtao Qu

Other affiliations: Xidian University
Bio: Jiangtao Qu is an academic researcher from University of Sydney. The author has contributed to research in topics: Materials science & Catalysis. The author has an hindex of 10, co-authored 52 publications receiving 470 citations. Previous affiliations of Jiangtao Qu include Xidian University.


Papers
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Journal ArticleDOI
TL;DR: Jingrun Ran, Jiangtao Qu, Hongping Zhang, Tian Wen, Hailong Wang, Shuangming Chen, Li Song, Xuliang Zhang, Liqiang Jing, Rongkun Zheng, Shi‐Zhang Qiao as discussed by the authors
Abstract: Jingrun Ran, Jiangtao Qu, Hongping Zhang, Tian Wen, Hailong Wang, Shuangming Chen, Li Song, Xuliang Zhang, Liqiang Jing, Rongkun Zheng, Shi‐Zhang Qiao

177 citations

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TL;DR: In this paper, a single-atom surface alloys with high surface densities (up to 8%) are anchored on the Cu host for efficient electrocatalytic CO2 reduction.
Abstract: Direct experimental observations of the interface structure can provide vital insights into heterogeneous catalysis. Examples of interface design based on single atom and surface science are, however, extremely rare. Here, we report Cu–Sn single-atom surface alloys, where isolated Sn sites with high surface densities (up to 8%) are anchored on the Cu host, for efficient electrocatalytic CO2 reduction. The unique geometric and electronic structure of the Cu–Sn surface alloys (Cu97Sn3 and Cu99Sn1) enables distinct catalytic selectivity from pure Cu100 and Cu70Sn30 bulk alloy. The Cu97Sn3 catalyst achieves a CO Faradaic efficiency of 98% at a tiny overpotential of 30 mV in an alkaline flow cell, where a high CO current density of 100 mA cm−2 is obtained at an overpotential of 340 mV. Density functional theory simulation reveals that it is not only the elemental composition that dictates the electrocatalytic reactivity of Cu–Sn alloys; the local coordination environment of atomically dispersed, isolated Cu–Sn bonding plays the most critical role. The understanding of catalytic reactions at the atomic interface is vital; however, the characterization and mechanism studies of atomically dispersed catalysts remain challenging. Here, the authors demonstrate Cu–Sn surface alloys with isolated Sn atoms on a Cu host to achieve efficient CO2 to CO conversion.

82 citations

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TL;DR: In this article, the authors showed that an enlarged attractive domain wall pinning strength results in substantial coercivity enhancement with little sacrifice of remanence and maximum energy product in the Cu-particle-alloyed magnet.

79 citations

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TL;DR: The ability of Co single atom decorated N-doped graphitic carbon shell encapsulated cobalt nanoparticle electrocatalyst (referred as Co@CoNC-900) to controllably produce syngas at low overpotentials during CO2RR is demonstrated.
Abstract: Controllable concomitant production of CO and H2 (syngas) during electrochemical CO2 reduction reactions (CO2RR) is expected to improve the commercial feasibility of the technology to mitigate CO2 emissions as the generated syngas can be converted into useful chemicals using the commercial Fischer-Tropsch (FT) process. Herein, we demonstrate the ability of a Co single-atom-decorated N-doped graphitic carbon shell-encapsulated cobalt nanoparticle electrocatalyst (referred as Co@CoNC-900) to controllably produce syngas at low overpotentials during CO2RR. Through the engineering and modulation of dual active sites for CO2RR (modified carbon shell with encapsulated Co) and hydrogen evolution reaction (Co-N4 moieties) within Co@CoNC by varying the annealing temperature, we are able to tune the H2: CO ratio from 1: 2 to 1: 1 to 3: 2 over a wide range of applied potentials (-0.5 V to -0.8 V versus reversible hydrogen electrode, RHE). This versatile control of H2: CO ratio in CO2RR reaction brings up significant opportunity of using CO2 and H2O and renewable energy for producing a range of chemicals.

68 citations

Journal ArticleDOI
12 Oct 2020
TL;DR: The development of highly active and reliable photocatalysts for solar hydrogen (H2) production requires the thorough and in-depth understanding of the atomic-level structure/composition-performanc... as discussed by the authors.
Abstract: The development of highly active and reliable photocatalysts for solar hydrogen (H2) production requires the thorough and in-depth understanding of the atomic-level structure/composition-performanc...

60 citations


Cited by
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TL;DR: This review overviews the recent developments of catalysis at single metal sites in MOF-based materials with emphasis on their structures and applications for thermocatalysis, electrocatalysis, and photocatalysis.
Abstract: Metal-organic frameworks (MOFs) are a class of distinctive porous crystalline materials constructed by metal ions/clusters and organic linkers. Owing to their structural diversity, functional adjustability, and high surface area, different types of MOF-based single metal sites are well exploited, including coordinately unsaturated metal sites from metal nodes and metallolinkers, as well as active metal species immobilized to MOFs. Furthermore, controllable thermal transformation of MOFs can upgrade them to nanomaterials functionalized with active single-atom catalysts (SACs). These unique features of MOFs and their derivatives enable them to serve as a highly versatile platform for catalysis, which has actually been becoming a rapidly developing interdisciplinary research area. In this review, we overview the recent developments of catalysis at single metal sites in MOF-based materials with emphasis on their structures and applications for thermocatalysis, electrocatalysis, and photocatalysis. We also compare the results and summarize the major insights gained from the works in this review, providing the challenges and prospects in this emerging field.

571 citations

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501 citations

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TL;DR: In this article, the authors present a rather comprehensive review of the recent research progress, in the view of associated value-added products upon selective electrocatalytic CO2 conversion.
Abstract: The continuously increasing CO2 released from human activities poses a great threat to human survival by fluctuating global climate and disturbing carbon balance among the four reservoirs of the biosphere, earth, air, and water. Converting CO2 to value-added feedstocks via electrocatalysis of the CO2 reduction reaction (CO2RR) has been regarded as one of the most attractive routes to re-balance the carbon cycle, thanks to its multiple advantages of mild operating conditions, easy handling, tunable products and the potential of synergy with the rapidly increasing renewable energy (i.e., solar, wind). Instead of focusing on a special topic of electrocatalysts for the CO2RR that have been extensively reviewed elsewhere, we herein present a rather comprehensive review of the recent research progress, in the view of associated value-added products upon selective electrocatalytic CO2 conversion. We initially provide an overview of the history and the fundamental science regarding the electrocatalytic CO2RR, with a special introduction to the design, preparation, and performance evaluation of electrocatalysts, the factors influencing the CO2RR, and the associated theoretical calculations. Emphasis will then be given to the emerging trends of selective electrocatalytic conversion of CO2 into a variety of value-added products. The structure-performance relationship and mechanism will also be discussed and investigated. The outlooks for CO2 electrocatalysis, including the challenges and opportunities in the development of new electrocatalysts, electrolyzers, the recently rising operando fundamental studies, and the feasibility of industrial applications are finally summarized.

387 citations

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TL;DR: A comprehensive review of the continuing efforts in exploring semiconductor nanowires for the assembly of functional nanoscale electronics and macroelectronics, including a unique design of solution-processable nanowire thin-film transistors for high-performance large-area flexible electronics.
Abstract: Semiconductor nanowires have attracted extensive interest as one of the best-defined classes of nanoscale building blocks for the bottom-up assembly of functional electronic and optoelectronic devices over the past two decades. The article provides a comprehensive review of the continuing efforts in exploring semiconductor nanowires for the assembly of functional nanoscale electronics and macroelectronics. Specifically, we start with a brief overview of the synthetic control of various semiconductor nanowires and nanowire heterostructures with precisely controlled physical dimension, chemical composition, heterostructure interface, and electronic properties to define the material foundation for nanowire electronics. We then summarize a series of assembly strategies developed for creating well-ordered nanowire arrays with controlled spatial position, orientation, and density, which are essential for constructing increasingly complex electronic devices and circuits from synthetic semiconductor nanowires. Next, we review the fundamental electronic properties and various single nanowire transistor concepts. Combining the designable electronic properties and controllable assembly approaches, we then discuss a series of nanoscale devices and integrated circuits assembled from nanowire building blocks, as well as a unique design of solution-processable nanowire thin-film transistors for high-performance large-area flexible electronics. Last, we conclude with a brief perspective on the standing challenges and future opportunities.

189 citations