“…In contrast, as shown in Figures 1g and S3a,b, the characteristic diffraction rings of AISe/ZnSe core/shell QDs match well with the (100), (002), (101), (102), (110), (103), and (112) planes of WZ ZnSe. It is observed that the diffraction pattern signals appeared to be more clear with the growth of ZnSe shell, which implies a better crystallinity of thicker ZnSe shell materials [28] . In addition, the crystal structure of as‐synthesized QDs (Figure 1h) is further investigated by X‐ray diffraction (XRD), in which the AISe core QDs exhibited a crystal structure that corresponds to zinc blend (ZB) AISe (JCPDS No.…”
Section: Resultsmentioning
confidence: 99%
“…It is observed that the diffraction pattern signals appeared to be more clear with the growth of ZnSe shell, which implies a better crystallinity of thicker ZnSe shell materials. [28] In addition, the crystal structure of as-synthesized QDs (Figure 1h) is further investigated by X-ray diffraction (XRD), in which the AISe core QDs exhibited a crystal structure that corresponds to zinc blend (ZB) AISe (JCPDS No. 23-0637), and the AISe/ZnSe core/shell QDs manifested typical diffraction peaks that match the WZ phase ZnSe (JCPDS No.15-0105).…”
Green" colloidal quantum dots (QDs)-based photoelectrochemical (PEC) cells are promising solar energy conversion systems possessing environmental friendliness, cost-effectiveness, and highly efficient solar-to-hydrogen conversion. In this work, ecofriendly AgInSe (AISe)/ZnSe core/shell QDs with wurtzite (WZ) phase were synthesized for solar hydrogen production. It was demonstrated that appropriately engineering the ZnSe shell thickness resulted in effective surface defects passivation of the AISe core for suppressed charge recombination in the consequent core/shell AISe/ZnSe QDs. The fabricated environmentally friendly core/shell QDs-based PEC device exhibited improved photo-excited electrons extraction efficiency under optimized conditions and delivered a maximum photocurrent density as high as 7.5 mA cm À 2 and long-term durability under standard AM 1.5G illumination (100 mW cm À 2 ). These findings suggest that AISe/ZnSe core/shell QDs with tailored optoelectronic properties are potential light sensitizers for eco-friendly, costeffective, and highly efficient solar energy conversion applications.[a] Z. Long, Prof.
“…In contrast, as shown in Figures 1g and S3a,b, the characteristic diffraction rings of AISe/ZnSe core/shell QDs match well with the (100), (002), (101), (102), (110), (103), and (112) planes of WZ ZnSe. It is observed that the diffraction pattern signals appeared to be more clear with the growth of ZnSe shell, which implies a better crystallinity of thicker ZnSe shell materials [28] . In addition, the crystal structure of as‐synthesized QDs (Figure 1h) is further investigated by X‐ray diffraction (XRD), in which the AISe core QDs exhibited a crystal structure that corresponds to zinc blend (ZB) AISe (JCPDS No.…”
Section: Resultsmentioning
confidence: 99%
“…It is observed that the diffraction pattern signals appeared to be more clear with the growth of ZnSe shell, which implies a better crystallinity of thicker ZnSe shell materials. [28] In addition, the crystal structure of as-synthesized QDs (Figure 1h) is further investigated by X-ray diffraction (XRD), in which the AISe core QDs exhibited a crystal structure that corresponds to zinc blend (ZB) AISe (JCPDS No. 23-0637), and the AISe/ZnSe core/shell QDs manifested typical diffraction peaks that match the WZ phase ZnSe (JCPDS No.15-0105).…”
Green" colloidal quantum dots (QDs)-based photoelectrochemical (PEC) cells are promising solar energy conversion systems possessing environmental friendliness, cost-effectiveness, and highly efficient solar-to-hydrogen conversion. In this work, ecofriendly AgInSe (AISe)/ZnSe core/shell QDs with wurtzite (WZ) phase were synthesized for solar hydrogen production. It was demonstrated that appropriately engineering the ZnSe shell thickness resulted in effective surface defects passivation of the AISe core for suppressed charge recombination in the consequent core/shell AISe/ZnSe QDs. The fabricated environmentally friendly core/shell QDs-based PEC device exhibited improved photo-excited electrons extraction efficiency under optimized conditions and delivered a maximum photocurrent density as high as 7.5 mA cm À 2 and long-term durability under standard AM 1.5G illumination (100 mW cm À 2 ). These findings suggest that AISe/ZnSe core/shell QDs with tailored optoelectronic properties are potential light sensitizers for eco-friendly, costeffective, and highly efficient solar energy conversion applications.[a] Z. Long, Prof.
“…1a, (ZnSe) 13 MSCs with a sharp absorption peak at 295 nm can be obtained by dispersing the pre-prepared ZnSe PCs in butane-1,4-diamine (BDA) at room temperature (about 25 °C), which is consistent with the reports in the literature. 40,41 The absorption peak of the (ZnSe) 13 MSCs disappears after standing for 2 h, indicating the poor stability of the (ZnSe) 13 MSCs in BDA solution.…”
Section: Resultsmentioning
confidence: 99%
“…S3, † a broad diffraction signal is observed in the X-ray diffraction (XRD) patterns of the (ZnSe) 13 MSCs or alloy Zn x Cd 13−x Se 13 MSCs, which suggests that the (ZnSe) 13 MSCs or alloy Zn x Cd 13−x Se 13 MSCs might be of relatively small size. 40,41 To further confirm the composition of the alloy MSCs prepared by cation exchange, X-ray photoelectron spectroscopy (XPS) spectra were recorded and are shown in Fig. S4.…”
Section: Resultsmentioning
confidence: 99%
“…Recently, Yu's group reported a two-step approach for MSCs, by which a series of binary ME MSCs (M = Zn or Cd, E = S, Se or Te) in a single-ensemble form have been facilely prepared. [35][36][37][38][39][40][41][42] In the two-step approach reported, precursor compounds (PCs) are first prepared at a relatively high temperature, and MSCs are then formed by dispersing the PCs in a specific solvent at a low temperature (usually at room temperature). Despite extensive efforts in the preparation of MSCs, the synthesis of alloyed MSCs has rarely been reported.…”
Magic-size clusters (MSCs) are molecular-like materials with unique properties at the border between molecules and solids, providing important insights into the nanocrystal formation process. However, the synthesis of multicomponent alloy...
A fundamental understanding of formation pathways is critical to the controlled synthesis of colloidal semiconductor nanocrystals. As ultrasmall‐size quantum dots (QDs) sometimes emerge in reactions along with magic‐size clusters (MSCs), distinguishing their individual pathway of evolution is important, but has proven difficult. To decouple the evolution of QDs and MSCs, an unconventional, selective approach has been developed, along with a two‐pathway model that provides a fundamental understanding of production selectivity. For on‐demand production of either ultrasmall QDs or MSCs, the key enabler is in how to allow a reaction to proceed in the time prior to nucleation and growth of QDs. In this prenucleation stage, an intermediate compound forms, which is the precursor compound (PC) to the MSC. Here, the two‐pathway model and the manipulation of such PCs to synthesize either ultrasmall QDs or binary and ternary MSCs are highlighted. The two‐pathway model will assist the development of nucleation theory as well as provide a basis for a mechanism‐enabled design and predictive synthesis of functional nanomaterials.
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