Wood is a natural renewable material with a porous structure widely used in construction, furniture, and interior decoration, yet its intrinsic flammability poses safety risks. Therefore, environmentally friendly flame retardants have received increasing attention. In this study, a water-soluble flame retardant, consisting of bio-resourced phytic acid (PA), hydrolyzed collagen (HC), and glycerol (GL), was used to improve the flame retardancy of wood (“PHG/wood”) through full cell vacuum-pressure impregnation. Morphology and Fourier transform infrared analysis results show that the flame retardant impregnated the wood and adhered evenly to the wood vessels. A PA/HC/GL ratio of 3:1:1 (concentration of the flame retardant solution = 30%) maximized the limiting oxygen index (LOI, 41%) and weight gain (51.32%) for PHG-C30/wood. The flame retardant formed an expansive layer after heating, and the treated wood showed an improved combustion safety performance such that the fire performance index and residue of PHG-C30/wood were 75 and 126.8% higher compared with that of untreated wood, respectively. The peak and total heat release were also significantly reduced by 54.7 and 47.7%, respectively. The PHG/wood exhibited good carbon-forming performance and a high degree of graphitization after combustion. The dense carbon layer provides condensed phase protective action, and non-combustible volatile gases, such as H2O, CO2, and NH3, are released simultaneously to dilute the fuel load in the gas phase. Thus, PHG is shown to be an effective flame retardant for wood.

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The elemental proportion of Cu poor and Zn rich in Cu2ZnSn(S,Se)4 (CZTSSe) is well established for achieving highly efficient CZTSSe solar cells. However, how high Zn/Sn ratio can the complicated CZTSSe thin film tolerate remains a question. Therefore, herein, the well control of Zn/Sn ratio in CZTSSe thin film is obtained by multi‐spin‐coating and tuning the initial Zn/Sn ratio in the Cu–Zn–Sn–S precursor ink from 1.0 to 1.9. It is found that the Zn/Sn on the surface of CZTSSe absorber can self‐regulate to around 1.2 even with Zn/Sn ratio up to 1.9 in the precursor solution. Excess Zn presented as Zn(S,Se) secondary phase not only concentrate near the bottom area, but also widely distribute at the grain boundaries (GBs). In addition, it is found that the Zn(S,Se) secondary phase at GBs can promote current transport as revealed by conductive atomic force microscopy measurement. The surface roughness and grain size of the resulting CZTSSe absorber increased, whereas the MoSe2 thickness was reduced with increasing Zn/Sn ratio. More importantly, the device performance increased from 4.5% to 10.0% with a significant decrease in VOC deficit from 0.73 to 0.58 V when the Zn/Sn ratio increases from 1.0 to 1.5 in the precursor ink.