Although hydrogenated amorphous silicon is already widely examined regarding its structural and electronic properties, the chemical etching behavior of this material is only roughly understood. We present a detailed study of the etching properties of intrinsic hydrogenated amorphous silicon, (i)a-Si:H, layers on crystalline silicon, c-Si, within the framework of metal assisted chemical etching (MACE) using silver nanoparticles (Ag NPs). The etching processes are examined by in situ photoluminescence (PL) and in situ surface photovoltage (SPV) measurements, as these techniques allow a monitoring of the hole injection that takes place during MACE. By in situ PL measurements and SEM images, we could interpret the different stages of the MACE process of (i)a-Si:H layers and determine etch rates of (i)a-Si:H, that are found to be influenced by the size of the Ag NPs. In situ PL and in situ SPV measurements both enable researchers to determine when the Ag NPs reach the (i)a-Si:H/c-Si interface. Furthermore, a preferential MACE of (i)a-Si:H versus c-Si is revealed for the first time. This effect could be explained by an interplay of the different thermodynamic and structural properties of the two materials as well as by hole injection during MACE resulting in a field effect passivation. The presented results allow an application of the examined MACE processes for Si nanostructuring applications.
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http://dx.doi.org/10.1021/acsami.5b02922 | DOI Listing |
Langmuir
November 2024
School of Materials Science and Engineering, National Institute for Advanced Materials, TKL of Metal and Molecule-Based Material Chemistry, Nankai University, Tianjin 300350, PR China.
Despite their high surface area, remarkable porosity, and efficient charge transfer mechanisms, conductive MOFs have found limited utilization within the domain of photocatalysis. In this study, we synthesized a cutting-edge S-type Ni(HITP)/TiO heterojunction photocatalyst exhibiting outstanding light harvesting and prolonged lifetime of photogenerated electrons through an in situ synthesis approach. Compared with TiO, the composite materials not only significantly increase the specific surface area by 4.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan 750021, PR China; Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan 750021, PR China; Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.
Designing efficient sulfide photocatalysts for the simultaneous split water into H and O continue to be an arduous challenge. Herein, a Zn-vacancy mediated S-scheme MnCdS/ZnS-V heterojunction derived from MnCdS/MOF-5 via in-situ vulcanization of MOF-5 in a new-fashioned sacrificial reagent of NaS/NaHPO was fabricated. The presence of Zn vacancy (V) was certified by TEM, XPS, EPR and PL results, which result in a new defect level in the band structure of ZnS.
View Article and Find Full Text PDFJACS Au
November 2023
School of Physics and Physical Engineering, Qufu Normal University, Qufu 273165, China.
Given the rapid recombination of photogenerated charge carriers and photocorrosion, transition metal sulfide photocatalysts usually suffer from modest photocatalytic performance. Herein, S-vacancy-rich ZnInS (V-ZIS) nanosheets are integrated on 3D bicontinuous nitrogen-doped nanoporous graphene (N-npG), forming 3D heterostructures with well-fitted geometric configuration (V-ZIS/N-npG) for highly efficient photocatalytic hydrogen production. The V-ZIS/N-npG presents ultrafast interfacial photogenerated electrons captured by the S vacancies in V-ZIS and holes neutralization behaviors by the extra free electrons in N-npG during photocatalysis, which are demonstrated by in situ XPS, femtosecond transient absorption (fs-TA) spectroscopy, and transient-state surface photovoltage (TS-SPV) spectra.
View Article and Find Full Text PDFJ Colloid Interface Sci
November 2023
Institute of Physical Chemistry, College of Chemistry, Jilin University, Changchun 130012, PR China. Electronic address:
Ti-ZnFeO photoanode has attracted extensive attention in photoelectrochemical (PEC) water oxidation due to its narrow band gap and good photostability. However, its low efficiency limits its development. Herein, we designed and constructed direct Z-scheme Ti-ZnFeO/InO (Ti-ZFO/InO) photoanode.
View Article and Find Full Text PDFSmall
October 2023
School of Environmental Sciences and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, 710021, China.
How to collaboratively reduce Cr(VI) and break Cr(III) complexes is a technical challenge to solve chromium-containing wastewater (CCW) pollution. Solar photovoltaic (SPV) technology based on semiconductor materials is a potential strategy to solve this issue. Sb S is a typical semiconductor material with total visible-light harvesting capacity, but its large-sized structure highly aggravates disordered photoexciton migration, accelerating the recombination kinetics and resulting low-efficient photon utilization.
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