Shamsiya Shams, B. Bindhu, Adhigan Murali, R. Ramesh, Abdullah Al Souwaileh and Sung Soo Han
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引用次数: 0
Abstract
Two-dimensional (2D) hybrid materials, particularly those based on boron nitride (BN) and graphene oxide (GO), have attracted significant attention for energy applications owing to their distinct structural and electronic properties. BN/GO composites uniquely combine the mechanical strength, thermal stability and electrical insulation of BN with the high conductivity and flexibility of GO, creating advanced materials ideal for the fabrication of batteries, supercapacitors and fuel cells. These hybrids offer synergistic effects, enhanced charge transport, increased surface area, and improved chemical stability, making them promising candidates for high-performance energy systems. Despite their potential, challenges, such as achieving scalable synthesis and uniform BN–GO dispersions and poor interface compatibility, have limited the widespread adoption of BN–GO hybrids. To address these limitations, this study is focused on the scalable synthesis of BN–GO composites via a liquid-phase exfoliation method with ultrasonication, followed by preparation of sodium thiosulfate (STS)-functionalized BN–GO composites (STBG), which exhibited high electrochemical properties suitable for energy storage. The structural identification was confirmed using FT-IR, Raman, XRD, and UV-vis spectroscopy. Thermal stability of the samples was assessed by TGA, while their morphological analysis was performed using HR-TEM, TEM, and SEM. Pristine BN showed negligible efficiency, whereas STS functionalization elevated the efficiency of STBN to 81.7%, while the incorporation of GO in STBG1 and STBG2 boosted their efficiency to 89.3% and 83.3%, respectively. STBG1 exhibited a nearly rectangular, symmetrical CV curve at various scan rates, demonstrating excellent capacitive behavior. Furthermore, it achieved the highest specific capacitance of 115.82 F g−1 at a current density of 1 A g−1, together with a coulombic efficiency of 89.3%, indicating its superior charge transfer and minimal energy loss. Additionally, STBG1 retained 87.3% of its capacity, while STBG2 retained 81.7% even after 3000 charge/discharge cycles. These findings highlight that STBG1 is a promising composite with high capacitance, strong rate capability, and exceptional coulombic efficiency, making it a viable candidate for next-generation energy storage systems.
二维(2D)杂化材料,特别是基于氮化硼(BN)和氧化石墨烯(GO)的杂化材料,由于其独特的结构和电子特性,在能源应用方面引起了极大的关注。BN/GO复合材料独特地将BN的机械强度、热稳定性和电绝缘性与GO的高导电性和柔韧性结合在一起,创造了制造电池、超级电容器和燃料电池的理想材料。这些混合材料具有协同效应、增强电荷传输、增加表面积和提高化学稳定性,使其成为高性能能源系统的有希望的候选者。尽管具有潜力,但诸如实现可扩展合成和均匀的BN-GO分散体以及界面兼容性差等挑战限制了BN-GO杂化物的广泛采用。为了解决这些限制,本研究的重点是通过超声液相剥离法可扩展合成BN-GO复合材料,然后制备硫代硫酸钠(STS)功能化BN-GO复合材料(STBG),该复合材料具有适合储能的高电化学性能。通过FT-IR, Raman, XRD和UV-vis光谱对其进行了结构鉴定。采用热重热分析(TGA)对样品进行热稳定性评价,并用HR-TEM、TEM和SEM对样品进行形貌分析。原始BN的效率可以忽略不计,而STS功能化将STBN的效率提高到81.7%,而在STBG1和STBG2中加入GO的效率分别提高到89.3%和83.3%。STBG1在不同扫描速率下呈现出近似矩形对称的CV曲线,表现出优异的电容性能。此外,在电流密度为1 a g-1时,它的比电容达到了最高的115.82 F g-1,库仑效率为89.3%,表明它具有优越的电荷转移和最小的能量损失。此外,在3000次充放电循环后,STBG1的容量保留率为87.3%,而STBG2的容量保留率为81.7%。这些发现突出表明,STBG1是一种有前途的复合材料,具有高电容、强速率能力和卓越的库仑效率,使其成为下一代储能系统的可行候选者。