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Abstract We explore the decay of bound neutrons in the JUNO liquid scintillator detector into invisible particles (e.g.,$$n\rightarrow 3 \nu $$ $n\to 3\nu$or$$nn \rightarrow 2 \nu $$ $nn\to 2\nu$), which do not produce an observable signal. The invisible decay includes two decay modes:$$ n \rightarrow { inv} $$ $n\to \mathrm{inv}$and$$ nn \rightarrow { inv} $$ $nn\to \mathrm{inv}$. The invisible decays ofs-shell neutrons in$$^{12}\textrm{C}$$ $_{}^{12}\text{C}$will leave a highly excited residual nucleus. Subsequently, some de-excitation modes of the excited residual nuclei can produce a time- and space-correlated triple coincidence signal in the JUNO detector. Based on a full Monte Carlo simulation informed with the latest available data, we estimate all backgrounds, including inverse beta decay events of the reactor antineutrino$${\bar{\nu }}_e$$ ${\overline{\nu }}_e$, natural radioactivity, cosmogenic isotopes and neutral current interactions of atmospheric neutrinos. Pulse shape discrimination and multivariate analysis techniques are employed to further suppress backgrounds. With two years of exposure, JUNO is expected to give an order of magnitude improvement compared to the current best limits. After 10 years of data taking, the JUNO expected sensitivities at a 90% confidence level are$$\tau /B( n \rightarrow { inv} ) > 5.0 \times 10^{31} \, \textrm{years}$$ $\tau /B(n\to \mathrm{inv})>5.0\times {10}^{31}\text{years}$and$$\tau /B( nn \rightarrow { inv} ) > 1.4 \times 10^{32} \, \textrm{years}$$ $\tau /B(nn\to \mathrm{inv})>1.4\times {10}^{32}\text{years}$. 

Abstract Smart materials with coupled optical and mechanical responsiveness to external stimuli, as inspired by nature, are of interest for the biomimetic design of the next generation of soft machines and wearable electronics. A tough polymer that shows adaptable and switchable mechanical and fluorescent properties is designed using a fluorescent lanthanide, europium (Eu). The dynamic Eu‐iminodiacetate (IDA) coordination is incorporated to build up the physical cross‐linking network in the polymer film consisting of two interpenetrated networks. Reversible disruption and reformation of Eu‐IDA complexation endow high stiffness, toughness, and stretchability to the polymer elastomer through energy dissipation of dynamic coordination. Water that binds to Eu³⁺ions shows an interesting impact simultaneously on the mechanical strength and fluorescent emission of the Eu‐containing polymer elastomer. The mechanical states of the polymer, along with the visually optical response through the emission color change of the polymer film, are reversibly switchable with moisture as a stimulus. The coupled response in the mechanical strength and emissive color in one single material is potentially applicable for smart materials requiring an optical readout of their mechanical properties.