“…Kesterite powder, Cu 2 ZnSn(S,Se) 4 , was synthesized in ampoules by mixing its constituents according to a previously described method by Shah and co‐workers, although other synthetic routes have been reported . Kesterite was obtained in form of a black mineral, easily pulverized manually.…”
Section: Resultsmentioning
confidence: 99%
“…Elements inside the quartz ampoule reacted for 48–72 h at 500 °C, in a tubular furnace or in a muffle . Finally, kesterite mineralized was obtained and characterized by X‐ray Fluorescence (XRF), Inductively Coupled Plasma Mass Spectrometry (ICP‐MS), Raman Spectroscopy and X‐ray Diffraction (XRD).…”
Section: Methodsmentioning
confidence: 99%
“…Development of CRM – free technology ensures a sustainable and circular economy, and that is why CZT(S)Se thin‐film PV devices are great candidates as an alternative to actual solar panels . Besides, CZT(S)Se thin‐film photovoltaic devices produce less energy consumption and low production costs than the conventional PV devices …”
The use of photovoltaic cells is constantly increasing and, in particular, a new generation of thin‐film photovoltaic (PV) cells is under development. The absorber of these new cells, kesterite (CZT(S)Se), is composed of abundant chemical elements. Nonetheless, the development of the recycling process for these elements is indispensable for circular economy. This research is focused on the recovery of selenium by thermal oxidation and subsequent reduction. Thus, recycling of selenium has been firstly studied on synthetic kesterite and then validated in a real sample of kesterite extracted from glass‐based PV cells. The best results were obtained in a vertical tubular furnace at 750 °C with an input of 20 mL/min of air. The posterior reduction process of selenium oxide was achieved by ascorbic acid, a common and economic reagent. Real kesterite was extracted from PV cells by thermal treatment at 90 °C for 1 hour to remove the encapsulant and ulterior treatment with HCl for the release of kesterite absorber. Optimal conditions from synthetic kesterite were applied to a real sample, recovering more than 90 % of selenium with a purity of 99.4 %.
“…Kesterite powder, Cu 2 ZnSn(S,Se) 4 , was synthesized in ampoules by mixing its constituents according to a previously described method by Shah and co‐workers, although other synthetic routes have been reported . Kesterite was obtained in form of a black mineral, easily pulverized manually.…”
Section: Resultsmentioning
confidence: 99%
“…Elements inside the quartz ampoule reacted for 48–72 h at 500 °C, in a tubular furnace or in a muffle . Finally, kesterite mineralized was obtained and characterized by X‐ray Fluorescence (XRF), Inductively Coupled Plasma Mass Spectrometry (ICP‐MS), Raman Spectroscopy and X‐ray Diffraction (XRD).…”
Section: Methodsmentioning
confidence: 99%
“…Development of CRM – free technology ensures a sustainable and circular economy, and that is why CZT(S)Se thin‐film PV devices are great candidates as an alternative to actual solar panels . Besides, CZT(S)Se thin‐film photovoltaic devices produce less energy consumption and low production costs than the conventional PV devices …”
The use of photovoltaic cells is constantly increasing and, in particular, a new generation of thin‐film photovoltaic (PV) cells is under development. The absorber of these new cells, kesterite (CZT(S)Se), is composed of abundant chemical elements. Nonetheless, the development of the recycling process for these elements is indispensable for circular economy. This research is focused on the recovery of selenium by thermal oxidation and subsequent reduction. Thus, recycling of selenium has been firstly studied on synthetic kesterite and then validated in a real sample of kesterite extracted from glass‐based PV cells. The best results were obtained in a vertical tubular furnace at 750 °C with an input of 20 mL/min of air. The posterior reduction process of selenium oxide was achieved by ascorbic acid, a common and economic reagent. Real kesterite was extracted from PV cells by thermal treatment at 90 °C for 1 hour to remove the encapsulant and ulterior treatment with HCl for the release of kesterite absorber. Optimal conditions from synthetic kesterite were applied to a real sample, recovering more than 90 % of selenium with a purity of 99.4 %.
“…Однако всегда существует вероятность образования других бинарных и тройных фаз из составляющих элементов в процессе роста CZTS [8]. Как видно из рис.…”
Представлены результаты исследований структурных и оптических свойств тонких пленок Cu 2 ZnSn(S,Se) 4 , полученных путем сульфитации (селенизации) пленок Cu 2 ZnSn, которые были напылены методом магне-тронного распыления на постоянном токе с использованием мишени Cu 2 ZnSn (99.99%) стехиометрического состава. Установлено, что тонкие пленки Cu 2 ZnSn(S,Se) 4 являются поликристаллическими с размерами зерен ∼ 60 nm. Определена оптическая ширина запрещенной зоны тонких пленок Cu 2 ZnSnS 4 (E
“…3) show the peaks shared by CZTS, ZnS, and Cu 2 SnS 3 (CTS). 17 Characteristic kesterite peak (101) 18 appears in samples A4 and A5, which denotes a higher degree of kesterite crystallization or less preferential orientation in these precursors. A small shoulder of the (100) peak is present in all the diffractograms.…”
Blister formation in Cu2ZnSnS4 (CZTS) thin films sputtered from a quaternary compound target is investigated. While the thin film structure, composition, and substrate material are not correlated to the blister formation, a strong link between sputtering gas entrapment, in this case argon, and blistering effect is found. It is shown that argon is trapped in the film during sputtering and migrates to locally form blisters during the high temperature annealing. Blister formation in CZTS absorbers is detrimental for thin film solar cell fabrication causing partial peeling of the absorber layer and potential shunt paths in the complete device. Reduced sputtering gas entrapment, and blister formation, is seen for higher sputtering pressure, higher substrate temperature, and change of sputtering gas to larger atoms. This is all in accordance with previous publications on blister formation caused by sputtering gas entrapment in other materials.
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