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Metal diborides as robust and highly stable electrodes for efficient electrocatalytic reduction of CO_(2) to CO in ionic liquid-based electrolytes
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作者 Yidan Mao Bingyu Li +10 位作者 Shuailing Ma siwen cui Zihan Zhang Pinwen Zhu Kongsheng Qi Xiaodong Li Weiwei Dong Wei Luo Rajeev Ahuja Dexin Yang Tian cui 《Chinese Chemical Letters》 2026年第4期289-295,共7页
The electrocatalytic reduction of carbon dioxide(CO_(2))into fuels holds significant promise for addressing energy and environmental challenges,albeit hindered by constraints in conversion efficiency,production rates,... The electrocatalytic reduction of carbon dioxide(CO_(2))into fuels holds significant promise for addressing energy and environmental challenges,albeit hindered by constraints in conversion efficiency,production rates,and electrode stability.Metal diborides are considered as promising electrocatalysts that may demonstrate superior CO_(2) electroreduction performance due to their distinctive electronic properties.Herein,a series of novel bulk metal diborides,encompassing transition metals from groupⅣB to groupⅦB elements,were fabricated using a high pressure-high temperature technique,which were directly utilized as self-supporting electrodes for electrocatalytic reduction of CO_(2).The zirconium diboride(ZrB_(2))electrode stood out in metal diborides with superior electrocatalytic activity in generating carbon monoxide(CO),achieving a Faradaic efficiency of 92.2%at-2.2 V vs.Ag/Ag^(+)in ionic liquid-based electrolytes.Impressively,the ZrB_(2) electrode demonstrated stable catalysis of CO_(2) reduction to CO over a nearly 60-h electrolysis period.Furthermore,the ZrB_(2) electrode and ionic liquid-based electrolytes could synergistically catalyze the reduction of CO_(2) to CO.Experimental results and density functional theory calculations support the notion that exposed metal sites on the ZrB_(2)(001)surface could enhance*CO desorption and restrain the hydrogen evolution reaction,thereby facilitating the conversion of CO_(2) into CO. 展开更多
关键词 Metal diborides Electrocatalytic reduction of CO_(2) Ionic liquids CO Self-supporting electrodes
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Triboelectrification based on double-layered polyaniline nanofibers for self-powered cathodic protection driven by wind 被引量:8
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作者 siwen cui Youbin Zheng +1 位作者 Jun Liang Daoai Wang 《Nano Research》 SCIE EI CAS CSCD 2018年第4期1873-1882,共10页
Polyaniline nanofibers (PANI NFs) are introduced to construct a wind-driven triboelectric nanogenerator (TENG) as a new power source for self-powered cathodic protection. PANI NFs serve as a friction layer to gene... Polyaniline nanofibers (PANI NFs) are introduced to construct a wind-driven triboelectric nanogenerator (TENG) as a new power source for self-powered cathodic protection. PANI NFs serve as a friction layer to generate charges by harvesting wind energy as well as a conducting layer to transfer charges in TENG. A PANI NFs-based TENG exhibits a high output performance with a maximum output voltage of 375 V, short current circuit of 248 μA, and corresponding power of 14.5 mW under a wind speed of 15 m/s. Additionally, a self-powered anticorrosion system is constructed by using a PANI-based TENG as the power source. The immersion experiment and electrochemical measurements demonstrate that carbon steel coupled with the wind-driven TENG is effectively protected with an evident open circuit potential drop and negative shift in the corrosion potential. The smart self-powered device is promising in terms of applications to protect metals from corrosion by utilizing wind energy in ambient conditions. 展开更多
关键词 POLYANILINE triboelectric nanogenerator WIND-DRIVEN SELF-POWERED cathodic protection
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High-pressure synthesis,mechanical properties,and oxidation behavior of advanced boron-containingα/β-Si_(3)N_(4)/Si ceramics using polymer-derived amorphous SiBN ceramics
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作者 Wei Li Shuailing Ma +10 位作者 siwen cui Jingxue Ding Marc Widenmeyer Xiaoqi Zhang Ying Zhan Zhaoju Yu Wenshu Zhang Pinwen Zhu Tian cui Anke Weidenkaff Ralf Riedel 《Journal of Advanced Ceramics》 SCIE EI CAS CSCD 2024年第10期1611-1621,共11页
The preparation of dense Si_(3)N_(4)-based ceramics has attracted great attention because of the achievable improvements in their mechanical properties and high-temperature oxidation resistance.In this work,advanced d... The preparation of dense Si_(3)N_(4)-based ceramics has attracted great attention because of the achievable improvements in their mechanical properties and high-temperature oxidation resistance.In this work,advanced dense boron-containingα/β-Si_(3)N_(4)/Si monoliths were prepared via a high pressure‒high temperature technique in which polymer-derived amorphous SiBN powders were used as raw materials.The crystallization behavior and phase transformation of the polymer-derived amorphous samples were studied in the temperature range from 1400 to 1800℃.The results demonstrate that the incorporation of boron in the Si_(3)N_(4)matrix suppresses the phase transformation fromα-Si_(3)N_(4)toβ-Si_(3)N_(4).Furthermore,the mechanical properties of the as-prepared samples were measured,and the maximum hardness and fracture toughness of boron-rich SiBN samples reached 14.8 GPa and 7.96 MPa·m1/2,respectively.The hardness of the obtained boron-rich SiBN samples is stable up to 300℃.In addition,the oxidation behavior of the samples prepared at 1400 and 1600℃ was investigated at 1400℃ for 50 h.The results show that the incorporation of boron significantly improved the oxidation resistance of the samples because of the formation of borosilicate/cristobalite.This work provides guidance for the synthesis of boron-containingα/β-Si_(3)N_(4)-based ceramics with excellent mechanical properties and oxidation resistance. 展开更多
关键词 high-pressure synthesis Si_(3)N_(4) mechanical properties oxidation resistance
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