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首页> 外文期刊>Chemistry Select >Heteroatom Engineering and Co-Doping of N and P to Porous Carbon Derived from Spent Coffee Grounds as an Efficient Electrocatalyst for Oxygen Reduction Reactions in Alkaline Medium
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Heteroatom Engineering and Co-Doping of N and P to Porous Carbon Derived from Spent Coffee Grounds as an Efficient Electrocatalyst for Oxygen Reduction Reactions in Alkaline Medium

机译:N和P的杂种工程和共掺杂到多孔碳,这些碳是源自咖啡的碳,作为碱性介质中还原反应的有效电催化剂

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This paper describes the synthesis of low cost electrocatalyst for oxygen reduction reaction (ORR) from spent coffee grounds (SCGs) through heteroatom engineering and simultaneous codoping of N and P. The co-doping of N and P to coffee carbon (N-P/CC) brings maximum defect sites in the catalyst which are favourable for ORR in relation to the individual heteroatom doped catalyst. Microscopic analysis confirms that N-P codoped coffee carbon (N-P/CC) undergoes slight structural changes by altering its porosity as well as surface area. Electrochemical studies confirm that, N-P/CC has superior catalytic activity with no effect to CO which makes it highly desirable as a metal-free electrocatalyst for ORR. The developed catalyst is subjected to 10,000 repeated potential cycles in alkaline media and is found only ~30 mV loss in its E1/2 potential, while the drop in E_(1/2) is about ~180 mV from its original value even after 1000 potential cycles for the commercial Pt/C catalyst. XPS analysis for NP/CC shows the presence of active pyridinic-N, graphitic-N species and active P-C and P-O bonds. Co-existence of all these species induces maximum polarization of C-C bonds in the carbon matrix and synergistically enhances the ORR behaviour in alkaline medium
机译:本文介绍了通过杂原具工程和N和P的同时辅助N和P的氧化咖啡地(SCG)的低成本电催化剂(ORR)的合成。在催化剂中带来最大的缺陷位点,这些缺陷位点有利于ORR相对于单个杂原掺杂催化剂。微观分析证实,N-P辅助咖啡碳(N-P/CC)通过改变其孔隙率和表面积会经历略有结构变化。电化学研究证实,N-P/CC具有优质的催化活性,对CO无效,这使其非常需要作为ORR的无金属电催化剂。开发的催化剂在碱性培养基中受到10,000个重复的电势循环的约束,其E1/2电位损失仅约30 mV,而E_(1/2)的下降即使在1000后即使在其原始值之后约为1​​80 mV商业PT/C催化剂的潜在循环。 NP/CC的XPS分析显示了活性吡啶-N,石墨N物种以及活性P-C和P-O键。所有这些物种的共存诱导碳基质中C-C键的最大极化,并协同增强了碱性培养基中的ORR行为

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