期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 4, 页码 1920-1928出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ta12675a
关键词
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资金
- Research and Technology Council of the Sharif University of Technology
- Iran National Science Foundation (INSF) [96011388]
- Iran Science Elites Federation [11/66332]
- Center for Condensed Matter Sciences (CCMS)
- Center of Atomic Initiative for New Materials (AI-Mat), National Taiwan University
A three-dimensional electrode based on porous Cu2O-Cu1.8S nanowires is prepared by means of a facile fabrication process. In this electrode, nanowires are decorated with Cu1.8S polyhedral nanostructures on the top, which are directly grown on a copper foam, thereby eliminating the need for a polymer binder. As an electrochemical electrode, it exhibits an extrinsic pseudocapacitive charge storage mechanism, which is different from that of battery-like Cu2O-CuO and Cu(OH)(2) electrodes. The areal and volumetric capacitances of the Cu2O-Cu1.8S electrode can reach 2.6 F cm(-2) and similar to 200 F cm(-3), respectively, at 2 mA cm(-2), which are much higher than those obtained using copper(i, ii) oxide and hydroxide phases. An asymmetric hybrid supercapacitor device shows areal and volumetric energy densities of 204.8 mu W h cm(-2) and similar to 2.1 mW h cm(-3), respectively, at a power density of 3.1 mW cm(-2) with a retention ratio of 55% at 15.5 mW cm(-2). Besides, both the Cu2O-Cu1.8S electrode and the asymmetric hybrid supercapacitor device exhibit remarkable long-term cycling stabilities, with the capacitance retention of 91% and 94% after 15 000 cycles at the current densities of 40 and 20 mA cm(-2), respectively. The porous copper sulfide phase in the fabricated electrode provides a reservoir of ions close to the surface, reducing the diffusion path lengths of ions into the electroactive solid network; this induces an improved electrochemical pseudocapacitive behavior. Our findings shed light on the role of surface modification for creating stable energy storage devices and present a simple way using cost-effective materials to generate more accessible active sites for charge storage on nanostructured electrodes.
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