ABSTRACT
Carbon nanotubes (CNTs) composed of bimetallic nickel-palladium (NiPd) nanoparticles encapsulated in graphitic carbon shells (NdPd@CNT) are prepared by the chemical vapour deposition method using waste polyethylene terephthalate (PET) plastic carbon sources and NiPd-decorated carbon sheets (NiPd@C) catalyst. The characterization results reveal that the face-centered cubic crystalline (fcc)-structured NiPd bimetallic alloy nanoparticles are encased by thin carbon nanotubes. The bimetallic synergism of NiPd nanoparticles actuates the outer CNT layers and accelerates the electrical conductivity, stimulating the electrochemical activity toward an effective hydrogen evolution reaction (HER). By virtue of the collective individualities of highly conductive aligned carbon walls and bimetallic active sites, the NiPd@CNT-equipped HER delivers a minimum overpotential of 87 mV and a Tafel slope value of 95 mV dec-1. The existing intact contact between NiPd and CNT facilitates continuous electron and ion transportation and firm stability toward long-term hydrogen production in HER. Notably, the NiPd@CNT reported here produces excellent electrochemical activity with minimal charge transference resistance, substantiating the efficacy of NiPd@CNT for futuristic green hydrogen production.
Subject(s)
Hydrogen , Nanotubes, Carbon , Nickel , Palladium , GasesABSTRACT
Advancements in photovoltaic research suggest that tin-based perovskites are potential alternatives to traditional lead-based structures. Cs2SnI6, specifically, stands out as a notable candidate, exhibiting impressive performance. However, its complete potential remains untapped primarily owing to the limited understanding of its photophysics. In light of this, this study aims to bridge this knowledge gap. To commence our study, we first executed theoretical investigations to locate the energetically diverse excitons within the Brillouin zone. Building on this knowledge, we then utilized transient absorption spectroscopy to investigate their temporal evolution. Herein, we observed the formation of high-energy excitons even when the incident photon energy was below the necessary threshold, which is quite distinctive and intriguing. Of particular interest is the generation of ultraviolet (UV) domain exciton using visible photons, which implies that Cs2SnI6 has the potential for efficient solar light harvesting. Tracking the kinetics revealed that this unique finding arises due to the intertwined formation and decay pathways undertaken by the different excitons, aided by intervalley scattering and phonon absorption processes. In addition, we found that the decay of the UV exciton was unusually slow. Transient mobility investigations were undertaken to probe the carrier transport behavior that further established hot carriers (HCs) in Cs2SnI6 to be highly mobile and susceptible to polaron formation. Overall, our findings demonstrate that Cs2SnI6 is a strong candidate for HC-based photovoltaics because it possesses all the prerequisites desired for such applications.
ABSTRACT
Mn-doped perovskites have already been widely explored in the context of interesting optical, electronic, and magnetic properties. Such fascinating traits showcased by them explain the huge augmentation in the device efficiency, directing their widespread application in the field of solar cells, energy- harvesting sectors, and light-emitting diodes. However, the underlying photophysics governing the overall charge carrier dynamics in Mn-doped CsPbBr3 nanoplatelets (NPLs) has never been discussed and therefore demands an in-depth investigation. Herein, fluorescence up-conversion and femtosecond transient absorption (TA) spectroscopy are employed for gaining a comprehensive understanding of the excited-state dynamics and the fundamental energy/charge-transfer processes for two-dimensional CsPbBr3 nanoplatelets (NPLs) and their Mn-doped counterparts. The up-conversion measurement clearly suggests the possibility of energy-transfer pathways in the Mn-doped CsPbBr3 NPLs. Interestingly, strong indication of charge transfer (CT) in Mn-doped CsPbBr3 NPLs was unambiguously established by an ultrafast TA approach. Our investigation clearly suggests that both the probable processes viz. the ultrafast energy and electron transfers noticeable in the Mn2+-doped CsPbBr3 NPLs are utterly competitive and rapid owing to the highly confined nature of the two-dimensional NPLs. This extensive probing of concurrent charge/energy-transfer processes may pave help clarify unresolved anomalies in Mn-doped perovskites, which may prove advantageous for a wide range of practical applicability.
