In standard fNIRS, a light source and a detector forming a channel have to be ~2-3cm apart. The light leaves the source, goes into the scalp in a banana shape due to refraction, and reaches the detector. The idea is that due to differential absorption of different wavelengths by oxygenated and deoxygenated haemoglobin, you can send 2 wavelengths and solving a 2x2 system gives you the fluctuations in oxygenated and deoxygenated haemoglobin in the tissue the light transversed. This is a proxy of brain activation in that area. If the neurons fire a lot, they consume more oxygen and the brain then sends more oxygen there, this is called Brain-oxygenation level depedent (BOLD) response. If the path length is too short, the light cannot get refracted deep enough to reach the cortex, so you do not measure brain. If it is longer, too much light is absorbed on the way and less signal reaches the detector. The researchers here try to detect light with source/detector diametrically opposite on the scalp, and they show they can. However, it is not clear what kind of application this can have. It was done under very restrictive conditions (subjects very light-skinned, no hair, 30 minutes recording). Moreover, an advantage of standard fNIRS is the high spatial specificity, and it is not clear how to actually translate the light intensity data in their case to brain activation (and probably it is going to be very noisy) as the light transverses all the head.
In any case, they are experimenting with a novel technique, more like a PoC that they can at least detect photons but nothing more than that, and we are probably far away from any potential applications, if any is even come out of this. But it could also lead to applications we cannot actually imagine right now. As for applying this to measure brain activity in the way current fNIRS and fMRI do, I am skeptical.