Durgadas Datta, Ramakanta Mondal, Ram Chandra Maji, Subin Yu, Dong-Il Won, Dong Ha Kim, Swarup Kumar Maji
{"title":"各向异性含二硫化钼的金纳米金字塔用于等离子体增强电催化、生物传感和能源生产。","authors":"Durgadas Datta, Ramakanta Mondal, Ram Chandra Maji, Subin Yu, Dong-Il Won, Dong Ha Kim, Swarup Kumar Maji","doi":"10.1039/d5nh00491h","DOIUrl":null,"url":null,"abstract":"<p><p>The strategic integration of anisotropic plasmonic nanostructures with two-dimensional (2D) semiconductors presents an emerging route for designing multifunctional hybrid systems with advanced photoelectrochemical (PEC) capabilities. In this work, we report the synthesis of a core-shell nanohybrid, Au nanobipyramid@MoS<sub>2</sub> (AuNBP@MoS<sub>2</sub>), wherein gold nanobipyramids are uniformly encapsulated by few-layer MoS<sub>2</sub> nanosheets. This architecture promotes direct plasmon-semiconductor coupling under 808 nm near-infrared (NIR) excitation, enabling efficient hot electron generation, enhanced interfacial charge separation, and photothermal-assisted transport <i>via</i> localized surface plasmon resonance (LSPR). When immobilized on a glassy carbon electrode (AuNBP@MoS<sub>2</sub>/GC), the hybrid device delivers exceptional PEC performance for both nonenzymatic biosensing and electrocatalysis. The sensor exhibits ultrasensitive detection of H<sub>2</sub>O<sub>2</sub> and glucose with wide linear ranges (10 μM-30 mM and 100 μM-8 mM), low detection limits (7.25 μM and 5.95 μM), and high sensitivities (376.86 and 23.42 μA mM<sup>-1</sup> cm<sup>-2</sup>), accompanied by ∼11-fold photocurrent enhancement under LSPR. It further enables selective HeLa cancer cell detection <i>via</i> biomarker-triggered H<sub>2</sub>O<sub>2</sub> release. In electrocatalysis, the hybrid electrode exhibits outstanding hydrogen evolution reaction (HER) activity, with a low onset potential (-0.18 V <i>vs.</i> RHE), an overpotential of -0.32 V at 10 mA cm<sup>-2</sup>, and a Tafel slope of 92 mV dec<sup>-1</sup> under NIR illumination. Addition of ethanol as a sacrificial agent further reduces the overpotential to -0.316 V and enhances the exchange current density by ∼12-fold due to suppressed charge recombination and improved hot carrier utilization. Mechanistic investigations combining experimental and theoretical analyses attribute these enhancements to synergistic plasmonic effects, efficient hot electron injection, and photothermal contributions. This work underscores the immense potential of anisotropic plasmonic-semiconductor hybrids in driving next-generation technologies for biosensing, electrocatalysis, and sustainable energy applications.</p>","PeriodicalId":93,"journal":{"name":"Nanoscale Horizons","volume":" ","pages":""},"PeriodicalIF":6.6000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anisotropic Au nanobypyramids with molybdenum disulfide for plasmon-enhanced electrocatalysis, biosensing and energy production.\",\"authors\":\"Durgadas Datta, Ramakanta Mondal, Ram Chandra Maji, Subin Yu, Dong-Il Won, Dong Ha Kim, Swarup Kumar Maji\",\"doi\":\"10.1039/d5nh00491h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The strategic integration of anisotropic plasmonic nanostructures with two-dimensional (2D) semiconductors presents an emerging route for designing multifunctional hybrid systems with advanced photoelectrochemical (PEC) capabilities. In this work, we report the synthesis of a core-shell nanohybrid, Au nanobipyramid@MoS<sub>2</sub> (AuNBP@MoS<sub>2</sub>), wherein gold nanobipyramids are uniformly encapsulated by few-layer MoS<sub>2</sub> nanosheets. This architecture promotes direct plasmon-semiconductor coupling under 808 nm near-infrared (NIR) excitation, enabling efficient hot electron generation, enhanced interfacial charge separation, and photothermal-assisted transport <i>via</i> localized surface plasmon resonance (LSPR). When immobilized on a glassy carbon electrode (AuNBP@MoS<sub>2</sub>/GC), the hybrid device delivers exceptional PEC performance for both nonenzymatic biosensing and electrocatalysis. The sensor exhibits ultrasensitive detection of H<sub>2</sub>O<sub>2</sub> and glucose with wide linear ranges (10 μM-30 mM and 100 μM-8 mM), low detection limits (7.25 μM and 5.95 μM), and high sensitivities (376.86 and 23.42 μA mM<sup>-1</sup> cm<sup>-2</sup>), accompanied by ∼11-fold photocurrent enhancement under LSPR. It further enables selective HeLa cancer cell detection <i>via</i> biomarker-triggered H<sub>2</sub>O<sub>2</sub> release. In electrocatalysis, the hybrid electrode exhibits outstanding hydrogen evolution reaction (HER) activity, with a low onset potential (-0.18 V <i>vs.</i> RHE), an overpotential of -0.32 V at 10 mA cm<sup>-2</sup>, and a Tafel slope of 92 mV dec<sup>-1</sup> under NIR illumination. Addition of ethanol as a sacrificial agent further reduces the overpotential to -0.316 V and enhances the exchange current density by ∼12-fold due to suppressed charge recombination and improved hot carrier utilization. Mechanistic investigations combining experimental and theoretical analyses attribute these enhancements to synergistic plasmonic effects, efficient hot electron injection, and photothermal contributions. 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Anisotropic Au nanobypyramids with molybdenum disulfide for plasmon-enhanced electrocatalysis, biosensing and energy production.
The strategic integration of anisotropic plasmonic nanostructures with two-dimensional (2D) semiconductors presents an emerging route for designing multifunctional hybrid systems with advanced photoelectrochemical (PEC) capabilities. In this work, we report the synthesis of a core-shell nanohybrid, Au nanobipyramid@MoS2 (AuNBP@MoS2), wherein gold nanobipyramids are uniformly encapsulated by few-layer MoS2 nanosheets. This architecture promotes direct plasmon-semiconductor coupling under 808 nm near-infrared (NIR) excitation, enabling efficient hot electron generation, enhanced interfacial charge separation, and photothermal-assisted transport via localized surface plasmon resonance (LSPR). When immobilized on a glassy carbon electrode (AuNBP@MoS2/GC), the hybrid device delivers exceptional PEC performance for both nonenzymatic biosensing and electrocatalysis. The sensor exhibits ultrasensitive detection of H2O2 and glucose with wide linear ranges (10 μM-30 mM and 100 μM-8 mM), low detection limits (7.25 μM and 5.95 μM), and high sensitivities (376.86 and 23.42 μA mM-1 cm-2), accompanied by ∼11-fold photocurrent enhancement under LSPR. It further enables selective HeLa cancer cell detection via biomarker-triggered H2O2 release. In electrocatalysis, the hybrid electrode exhibits outstanding hydrogen evolution reaction (HER) activity, with a low onset potential (-0.18 V vs. RHE), an overpotential of -0.32 V at 10 mA cm-2, and a Tafel slope of 92 mV dec-1 under NIR illumination. Addition of ethanol as a sacrificial agent further reduces the overpotential to -0.316 V and enhances the exchange current density by ∼12-fold due to suppressed charge recombination and improved hot carrier utilization. Mechanistic investigations combining experimental and theoretical analyses attribute these enhancements to synergistic plasmonic effects, efficient hot electron injection, and photothermal contributions. This work underscores the immense potential of anisotropic plasmonic-semiconductor hybrids in driving next-generation technologies for biosensing, electrocatalysis, and sustainable energy applications.
期刊介绍:
Nanoscale Horizons stands out as a premier journal for publishing exceptionally high-quality and innovative nanoscience and nanotechnology. The emphasis lies on original research that introduces a new concept or a novel perspective (a conceptual advance), prioritizing this over reporting technological improvements. Nevertheless, outstanding articles showcasing truly groundbreaking developments, including record-breaking performance, may also find a place in the journal. Published work must be of substantial general interest to our broad and diverse readership across the nanoscience and nanotechnology community.