“…Figure shows the crystal structure data of pristine h‐BN powders, as‐prepared h‐BNNSs, OH‐BNNSs, APTS‐BNNSs, and CPBA‐BNNSs. In Figure a, it is clearly indicated that the X‐ray diffraction (XRD) pattern of the h‐BN has six characteristic diffraction peaks at 26.9°, 41.6°, 43.8°, 50.2°, 55.2°, and 76.0°, and they are attributed to (002), (100), (101), (102), (004), and (110) planes of hexagonal crystal structure (JCPDS card 34‐0421), respectively . Compared with the pristine h‐BN, the as‐exfoliated h‐BNNSs and surface‐modified h‐BNNSs exhibit the similar characteristic diffraction peaks.…”