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您的检索式：作者名="Chen Shukang"
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| 1 | A Controller of Bruthlcss DC Motor Used for Hybid Electric Vehicle显示文摘 | Hongxin Wu Shukang chen | 2005 | IEEE transactions on May2005，4，1： | 1 |
| 2 | Upgrading CO_(2) into acetate on Bi_(2)O_(3)@carbon felt integrated electrode via coupling electrocatalysis with microbial synthesis显示文摘Upgrading of atmospheric CO_(2) into high-value-added acetate using renewable electricity via electrocatalysis solely remains a great challenge.Here,inspired by microbial synthesis via biocatalysts,we present a coupled system to produce acetate from CO_(2) by bridging inorganic electrocatalysis with microbial synthesis through formate intermediates.A 3D Bi_(2)O_(3)@CF integrated electrode with an ice-sugar gourd shape was fabricated via a straightforward hydrothermal synthesis strategy,wherein Bi_(2)O_(3) microspheres were decorated on carbon fibers.This ice-sugar gourd-shaped architecture endows electrodes with multiple structural advantages,including synergistic contribution,high mass transport capability,high structural stability,and large surface area.Consequently,the resultant Bi_(2)O_(3)@CF exhibited a maximum Faradic efficiency of 92.4%at−1.23 V versus Ag/AgCl for formate generation in 0.5 M KHCO_(3),exceeding that of Bi_(2)O_(3)/CF prepared using a conventional electrode preparation strategy.Benefiting from the high formate selectivity,unique architecture,and good biocompatibility,the Bi_(2)O_(3)@CF electrode attached with enriched CO_(2)-fixing electroautotrophs served as a biocathode.As a result,a considerable acetate yield rate of 0.269±0.009 g L^(−1) day^(−1)(a total acetate yield of 3.77±0.12 g L^(−1) during 14-day operation)was achieved in the electrochemical–microbial system equipped with Bi_(2)O_(3)@CF. | Xiaojing Liu Kang Zhang Yidan Sun Shukang Zhang Zhenyu Qiu Tianshun Song Jingjing Xie Yuping Wu Yuhui Chen | 2023 | SusMat2023，3，2： | 1 |
| 3 | Synthesis of HFC-134a over CrF3/AlF3 catalysts显示文摘 | Jian Lu Huie Yang Chen Shukang | 1996 | Catal Lett1996，41，： | 1 |
| 4 | Deconstructing Vibrational Motions on the Potential Energy Surfaces of Hydrogen-Bonded Complexes显示文摘Internal vibrations underlie transient structure formation,spectroscopy,and dynamics.However,at least two challenges exist when aiming to elucidate the contributions of vibrational motions on the potential energy surfaces.One is the acquisition of well-resolved experimental infrared spectra,and the other is the development of efficient theoretical methodologies that reliably predict band positions,relative intensities,and substructures.Here,we report size-specific infrared spectra of ammonia clusters to address these two challenges.Unprecedented agreement between experiment and state-of-the-art quantum simulations reveals that the vibrational spectra are mainly contributed by proton-donor ammonia.A striking Fermi resonance observed at approximately 3210 and 3250 cm^(−1)originates from the coupling of NH symmetric stretch fundamentals with overtones of free and hydrogen-bonded NH bending,respectively.These novel,intriguing findings contribute to a better understanding of vibrational motions in a large variety of hydrogen-bonded complexes with orders of magnitude improvements in spectral resolution,efficiency,and specificity. | Bingbing Zhang Shuo Yang Qian-Rui Huang Shukang Jiang Rongjun Chen Xueming Yang Dong H.Zhang Zhaojun Zhang Jer-Lai Kuo Ling Jiang | 2021 | CCS Chemistry2021，3，1： | 0 |
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